Health And Family Welfare Department has published Supply Of Laboratory Items - Total Item No 1 To 2316(Part 1:- Item No 1 To 350)- Pro-Clacitonin,Ferritin,D-Dimer,Vitamin B12,Vitamin B3,Troponin I & T (Quanitative),Beta Hcg,Beta 2 Microglobulin,Alpha 1 Antitrypsin,Apo-Lipoprotein A1 & B,Ceruloplasmin,Hep. Submission Date for this Tender is 17-08-2023. Laboratory Electrophoresis and Blotting System Tenders in Vadodara Gujarat. Bidders can get complete Tender details and download the document.
Sr No | CorrigendumDate | Corrignedum | CorrigendumType | NewSubmissionDate |
1 | 31-Jul-2023 | 17-08-2023 |
Sl. No. | Item Title | Specification |
1 | Pro-Clacitonin | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
2 | ferritin | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
3 | D-dimer | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
4 | Vitamin B12 | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
5 | Vitamin B3 | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
6 | Troponin I & T (Quanitative) | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
7 | Beta HCG | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
8 | Beta 2 microglobulin | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
9 | Alpha 1 Antitrypsin | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
10 | Apo-Lipoprotein A1 & B | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
11 | Ceruloplasmin | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
12 | Heptoglobin | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
13 | BNP | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
14 | Lipoprotein A | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
15 | Insulin | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
16 | PTH | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
17 | Vitamin D | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
18 | Zinc | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
19 | Ammonia | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
20 | Total Iron | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
21 | hs-CRP | Based on Immunoturbidimetry method &Compatible with Fully Automated Biochemistry analyzer Erba XL- 640/ Mindray Bs-430 |
22 | Pro-Clacitonin | Automated Chemileuminisecence based Immunoassay test |
23 | IL-6 | Automated Chemileuminisecence based Immunoassay test |
24 | D-dimer | Automated Chemileuminisecence based Immunoassay test |
25 | Vitamin B12 | Automated Chemileuminisecence based Immunoassay test |
26 | Vitamin B3 | Automated Chemileuminisecence based Immunoassay test |
27 | Troponin I & T (Quanitative) | Automated Chemileuminisecence based Immunoassay test |
28 | Beta HCG | Automated Chemileuminisecence based Immunoassay test |
29 | Beta 2 microglobulin | Automated Chemileuminisecence based Immunoassay test |
30 | Alpha 1 Antitrypsin | Automated Chemileuminisecence based Immunoassay test |
31 | Apo-Lipoprotein A1 | Automated Chemileuminisecence based Immunoassay test |
32 | Apo-Lipoprotein B | Automated Chemileuminisecence based Immunoassay test |
33 | Ceruloplasmin | Automated Chemileuminisecence based Immunoassay test |
34 | Heptoglobin | Automated Chemileuminisecence based Immunoassay test |
35 | Lipoprotein A | Automated Chemileuminisecence based Immunoassay test |
36 | Transferrin | Automated Chemileuminisecence based Immunoassay test |
37 | Galactin-3 | Automated Chemileuminisecence based Immunoassay test |
38 | Estradiol | Automated Chemileuminisecence based Immunoassay test |
39 | Progesterone | Automated Chemileuminisecence based Immunoassay test |
40 | Prolactin | Automated Chemileuminisecence based Immunoassay test |
41 | AMH | Automated Chemileuminisecence based Immunoassay test |
42 | Testosterone | Automated Chemileuminisecence based Immunoassay test |
43 | C-Peptide | Automated Chemileuminisecence based Immunoassay test |
44 | Cortisol | Automated Chemileuminisecence based Immunoassay test |
45 | Insulin | Automated Chemileuminisecence based Immunoassay test |
46 | PTH | Automated Chemileuminisecence based Immunoassay test |
47 | Vitamin D3 | Automated Chemileuminisecence based Immunoassay test |
48 | TSH | Automated Chemileuminisecence based Immunoassay test |
49 | Free T4 | Automated Chemileuminisecence based Immunoassay test |
50 | Free T4 | Automated Chemileuminisecence based Immunoassay test |
51 | Anti- TPO | Automated Chemileuminisecence based Immunoassay test |
52 | Lactate | Automated Chemileuminisecence based Immunoassay test |
53 | Fructosamine | Automated Chemileuminisecence based Immunoassay test |
54 | UIBC | Automated Chemileuminisecence based Immunoassay test |
55 | TIBC | Automated Chemileuminisecence based Immunoassay test |
56 | PSA (Total) | Automated Chemileuminisecence based Immunoassay test |
57 | PSA (Free) | Automated Chemileuminisecence based Immunoassay test |
58 | FSH | Automated Chemileuminisecence based Immunoassay test |
59 | LH | Automated Chemileuminisecence based Immunoassay test |
60 | Leptin | Automated Chemileuminisecence based Immunoassay test |
61 | Adiponectine | Automated Chemileuminisecence based Immunoassay test |
62 | Zinc | Automated Chemileuminisecence based Immunoassay test |
63 | Inhibin | Automated Chemileuminisecence based Immunoassay test |
64 | CA 27.29 | Automated Chemileuminisecence based Immunoassay test |
65 | CA 15.3 | Automated Chemileuminisecence based Immunoassay test |
66 | CA 19-9 | Automated Chemileuminisecence based Immunoassay test |
67 | CEA | Automated Chemileuminisecence based Immunoassay test |
68 | Ca 125 | Automated Chemileuminisecence based Immunoassay test |
69 | AFP | Automated Chemileuminisecence based Immunoassay test |
70 | Cystatin C | Automated Chemileuminisecence based Immunoassay test |
71 | BNP | Compatible with ELISA Reader and Washer. |
72 | Transferrin | Compatible with ELISA Reader and Washer. |
73 | Galactin-3 | Compatible with ELISA Reader and Washer. |
74 | Estradiol | Compatible with ELISA Reader and Washer. |
75 | Progesterone | Compatible with ELISA Reader and Washer. |
76 | Prolactin | Compatible with ELISA Reader and Washer. |
77 | AMH | Compatible with ELISA Reader and Washer. |
78 | Testosterone | Compatible with ELISA Reader and Washer. |
79 | C-Peptide | Compatible with ELISA Reader and Washer. |
80 | Cortisol | Compatible with ELISA Reader and Washer. |
81 | Insulin | Compatible with ELISA Reader and Washer. |
82 | PTH | Compatible with ELISA Reader and Washer. |
83 | Vitamin D | Compatible with ELISA Reader and Washer. |
84 | Free T3 | Compatible with ELISA Reader and Washer. |
85 | Free T4 | Compatible with ELISA Reader and Washer. |
86 | Lactate | Compatible with ELISA Reader and Washer. |
87 | Fructosamine | Compatible with ELISA Reader and Washer. |
88 | UIBC | Compatible with ELISA Reader and Washer. |
89 | TIBC | Compatible with ELISA Reader and Washer. |
90 | PSA (Total &Free) | Compatible with ELISA Reader and Washer. |
91 | FSH | Compatible with ELISA Reader and Washer. |
92 | LH | Compatible with ELISA Reader and Washer. |
93 | Leptin | Compatible with ELISA Reader and Washer. |
94 | Adiponectine | Compatible with ELISA Reader and Washer. |
95 | Zinc | Compatible with ELISA Reader and Washer. |
96 | Ammonia | Compatible with ELISA Reader and Washer. |
97 | Measuring Cartridge | Compatible with ABG analyzer RAPID Point 500e |
98 | Wash Cartridge | Compatible with ABG analyzer RAPID Point 500e |
99 | Sample Cup | Compatible with Fully Automated analyzer Erba XL- 640/ Mindray Bs-430 |
100 | Auto wash | Compatible with Fully Automated Analyzer Erba Xl-640 |
101 | Acid -Alkaline Wash | Compatible with Fully Automated Analyzer Erba Xl-640 |
102 | Cuvette | Compatible with Fully Automated analyzer Erba XL- 640 |
103 | Cuvette | Compatible with Fully Automated analyzer Mindray Bs-430 |
104 | Reagent Bottle | 20 ml size bottle & compatible with Fully Automated analyzer Erba XL- 6400 |
105 | Reagent Bottle | 40 ml size bottle & compatible with Fully Automated analyzer Erba XL- 6400 |
106 | Reagent Bottle | 20 ml size bottle & compatible with Fully Automated analyzer Mindray Bs-430 |
107 | Reagent Bottle | 40 ml size bottle & compatible with Fully Automated analyzer Mindray Bs-430 |
108 | CD-8 Wash Solution | Compatible with Fully Automated Analyzer Mindray BS-430 |
109 | Electrolyte Reagent Pack | Compatible with Acculyte 3P Electrolyte Analyzer |
110 | Deproteinizer | Compatible with Acculyte 3P Electrolyte Analyzer |
111 | Heparinized Glass capillaries for Bill-P Bilirubinometer | Compatible with Bill-P Bilirubinometer |
112 | Serum Iron estimation kit* | Based on Ferrozine Colorimetric End Point Method, R1 & R2 reagent, liquid reagent,linearity 1000 µg/dI |
113 | Serum Ferritin estimation kit* | Based on Immunoturbidimetric method, R1 & R2 reagent,liquid reagent, linearity 600 µg/dI |
114 | Hank’s Balanced Salt Solution 10 X With Phenol red without Sodium bicarbonate | As per Column no.2 |
115 | D-dimer (Quantitative estimation of D-dimer based on turbidimetric immunoassay. R1 & R2 liquid reagent , measuring the range of 200-4000 ng/ml, linearity 10000 ng/ml | As per Column no.2 |
116 | Hb-sensor unit | Original |
117 | Hb-sensor casing | Original |
118 | Photo-electric sensor device(LS) | Original |
119 | device for specimen input (DS) | Original |
120 | Waste bottle sensor device with cable | Original |
121 | Plasma GLUCOSE Estimation kit based on GOD-POD ENZYMATIC End – point method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid / Lypholysed Reagents.Adaptable to Endpoint 505 nm / Fixed time Kinetic method. GOD = 8 U/mL, Peroxidase = 0.6 U/L, Linearity = 500 mg/dL, Std : 100 mg/dL Sensitivity =1 mg/dL. CV < 2 %. Compatible to Semi Auto and Miura Fully Auto Analysers. Long expiry date & stability. Reagent stable for atleast 4 weeks after reconstitution. |
122 | Plasma GLUCOSE Estimation kit based on HEXOKINASE ENZYMATIC UV Method (2 point analysis) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. Hexokinase-UV-End Point 340 nm Method. Hexokinase>1500 U/L, G6PDH>3000 U/L, NAD>2mmol/L Linearity = 500 mg/dL Std :100 / 200 mg/dL CV < 5 %. Compatible with Miura Fully Auto + Semi Auto Analysers. Long expiry date & stability. |
123 | Serum Ferritin Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
124 | Serum UREA Estimation Kit Based on GLDH ENZYMATIC UV KINETIC METHOD (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. GLDH UV-Kinetic Method. Urease>6000 U/L, Linearity : 300 mg / dL. Sensitivity = 2 mg/dL. %CV= 1. Compatible with Miura Fully Auto + Semi Auto Analysers. |
125 | Serum UREA Estimation Kit Based on GLDH ENZYMATIC UV KINETIC METHOD (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. GLDH UV-Kinetic Method. Urease>6000 U/L, Linearity : 300 mg / dL. Sensitivity = 2 mg/dL. %CV= 1. Compatible with Miura Fully Auto + Semi Auto Analysers. |
126 | Serum UREA Estimation Kit Based on MODIFIED BERTHELOT METHOD (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. Modified Berthelot Method. Urease>4 U/L, Linearity : 300 mg / dL. Sensitivity = 2 mg/dL. CV < 1% Compatible with Miura Fully Auto + Semi Auto Analysers. |
127 | Serum TOTAL CHOLESTEROL Estimation kit based on CHOD-POD ENZYMATIC End – point method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use, Single Reagent. Enzymatic - End Point 510 nm Method. Cholesterol Oxidase > 100 U / L., POD > 500 U / L., Linearity = 600 mg/dL. Sensitivity =4 mg/dL. %CV= 2 Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry & stable reagents. |
128 | Serum CREATININE Estimation Kit based on Jaffe’s Method 2-point rate reaction (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use & Single Reagent. Fixed-Rate 510 nm. Method Without Deproteinization.Picric acid = 9-10 mMol/L Standard : 2 mg / dL Linearity upto 20 mg/dL Sensitivity =0.2 mg/dL. %CV= 2. Compatible to Miura Fully Auto + Semi Auto Analysers. |
129 | Serum CREATININE Estimation Kit based on Enzymatic method(Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use & Single Reagent. Fixed-Rate 510 nm. Method Without Deproteinization.Picric acid = 9-10 mMol/L Standard : 2 mg / dL Linearity upto 20 mg/dL Sensitivity =0.2 mg/dL. %CV= 2. Compatible to Miura Fully Auto + Semi Auto Analysers. |
130 | Serum TOTAL PROTEIN Estimation Kit Based on BIURET Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready Use Single Reagent. Biuret - End Point 540 nm Method. Linearity: 15 Gm / dL Compatible with Miura Fully Auto + Semi Auto Analysers. |
131 | Serum ALBUMIN Estimation Kit Colorimetric B.C.G. Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Single Reagent. Colorimetric 630 nm End-Point Method. Succinate Buffer. BromoCresolGreen > 0.15mmol / L Standard 5 G / dL. Linearity 0.2-6 G / dL Sensitivity 0.02 g/L. Compatible with Miura AutoAnalyser & Semi Auto analyzers. |
132 | Serum TOTAL AND DIRECT BILIRUBIN Estimation kit based on JENDRASSIK & GROF Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use R1 & R2 Reagents. Colorimetric Diazo End Point 546 nm Jendrassik & Groff Method. Sulphanilic acid=5 mmol / L. Sufficient Nitrite Reagent. Two Point Calibrator within Kit. Onboard Stability of Working Reagents = 21 days. Linearity =25 mg/dL Sensitivity = 0.05 mg.% CV= 1.5 Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry date & stability. |
133 | Serum TOTAL AND DIRECT BILIRUBIN Estimation kit based on JENDRASSIK & GROF Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use R1 & R2 Reagents. Colorimetric Diazo End Point 546 nm Jendrassik & Groff Method. Sulphanilic acid=5 mmol / L. Sufficient Nitrite Reagent. Two Point Calibrator within Kit. Onboard Stability of Working Reagents = 21 days. Linearity =25 mg/dL Sensitivity = 0.05 mg.% CV= 1.5 Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry date & stability. |
134 | Serum Total Bilirubin Estimation kit for Fully Automated Biochemistry Analyzer (Single reagent) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Total bilirubin estimation kit compatible with Fully Automated Biochemistry Analyzer MIURA 2. Single reagent procedure 3. Reagent should be stabilized liquid form for ready to use. 4. Linearity: at least up to 15 mg/dL 5. Reagent stability: stable either at 2-8°C or at room temperature till date of expiry. Working reagent stable at least for 1 day. 6. Incubation time: not more than 10 minutes |
135 | Serum Direct Bilirubin Estimation kit for Fully Automated Biochemistry Analyzer (Single reagent) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Direct bilirubin estimation kit compatible with Fully Automated Biochemistry Analyzer MIURA 2. Single reagent procedure 3. Reagent should be stabilized liquid form for ready to use. 4. Linearity: at least up to 15 mg/dL 5. Reagent stability: stable either at 2-8°C or at room temperature till date of expiry. Working reagent stable at least for 1 day. 6. Incubation time: not more than 10 minutes |
136 | Serum ALP (Alkaline Phosphatase) Estimation Kit, AMP ( 2-Amino 2-Methyl 1-Propanol ) Buffer, Based on IFCC optimised KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Reagents. R1 & R2, Enzymatic - Kinetic 405 nm Method. Incubation : Only 1 Min. 1-Nitrophenylphosphate = 15 mmol / L Linearity > 700 U/L. Sensitivity = 5 U/L %CV = 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers.long expiry date & stability. |
137 | Serum ALP (Alkaline Phosphatase) Estimation Kit, DEA ( Diethanolamine ) Buffer (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Reagents. R1 & R2, Enzymatic - Kinetic 405 nm Method. Incubation : Only 1 Min. 1-Nitrophenylphosphate = 15 mmol / L Linearity > 700 U/L. Sensitivity = 5 U/L %CV = 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers. long expiry date & stability. |
138 | Serum SGOT Estimation Kit Based on IFCC optimised KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use, Single Reagent. Enzymatic - UV Kinetic 340 nm Method. ( IFCC ) Incubation : Only 1 Minute. w/o PLP. MDH>600 U/L , NADH>0.18mmol/L Linearity 5-600 U/L Sensitivity =5 IU/L. %CV= 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers Long Expiry & Stability. |
139 | Serum SGPT Estimation Kit Based on IFCC optimised KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Single Reagent. Enzymatic-UV Kinetic 340 nm Method.( IFCC). Linearity 5-400 U/L LDH>1200 U/L, NADH = 0.18mmol/L %CV= 2. Compatible with Miura AutoAnalyser & Semi Auto analyzers Long expiry & stability. |
140 | Serum CK-MB Estimation Kit Based on IFCC Kinetic Method (Immunoinhibition) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Stable Liquid or Lypholysed Reagent reconstitution stability 30 days at 2 - 8*C Immuno inhibition UV Kinetic Method. Linearity = 1500 U/L Required CK-MB Controls Level-1 & 2 must be given with Kit. Compatible with Miura AutoAnalyser & Semi Auto analyzers . |
141 | Serum Total CK Estimation Kit Based on IFCC UV Kinetic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Reagents R1 & R2. Enzymatic - Kinetic 340 nm, IFCC Method. Linearity = 1500 U/L Compatible with Miura AutoAnalyser & Semi Auto analyzers Long Expiry date & stability. |
142 | Serum LDH Estimation Kit Based on IFCC KINETIC Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use R1 & R2 Reagents. UV - Kinetic 340 nm Modified Wacker Method. Linearity : 1000 U/L Compatible with Miura Fully Auto + Semi Auto Analyser. Long expiry date & stability. |
143 | Serum GGT Estimation Kit Based on IFCC Kinetic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Reagents. R1 & R2, Enzymatic-Kinetic 405 nm Method.Glycylglycine > 100 mmol / L Linearity upto 1000 U / L. Compatible with Miura Fully Automated Analysers. Long expiry date & stability. |
144 | Serum HDL Precipitation reagent based on Polyethylene Glycol (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagent should be stabilized liquid form 2. Should be stable at room temperature till the date of expiry 3. Sample : Precipitating reagent ratio should be 1:1 4. To be supplied with HDL cholesterol standard: 40 or 50 mg/dL or calibrator 5 mL standard to be provided per 50 mL of reagent. 5. Linearity not less than 150 mg/dL.HDL Calibrator must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers |
145 | Serum HDL Estimation Kit Direct Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagents should be stabilized liquid form ready to use 2. To be supplied with HDL cholesterol calibrator 3. Linearity not less than 150 mg/dL.HDL Calibrator must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers |
146 | Serum LDL Estimation Kit Direct Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use R1 & R2 Reagents.Direct Enzymatic 600 nm. Colorimetric Method. Incubation : Only 5 Minutes. Linearity = 400mg/dL Calibrator for LDL must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers. |
147 | Serum TRIGLYCERIDE Estimation Kit based on GPO-PAP Enzymatic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Single Reagents. Enzymatic-End Point 505nm, 37"C Method. Incubation : Only 5 Min. LP.Lipase>2000U/L, POD>500U/L TG Calibrator : 200 or 300 mg/dL must be given with kit. Linearity :1000 mg/dL Compatible with Miura Fully Auto + SemiAuto Analysers. |
148 | Serum TOTAL CALCIUM Estimation Kit based on Arsenazo III Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready Use Single Reagent. Arsenazo III Colorimetric 650 nm Endpoint Method. Incubation : Only 1 Min. Arsenazo III > 0.12 mmol / L. Linearity = 15 mg/dL Standard : 10 mg / dL. Sensitivity 0.4 mg/dL.%CV= 1.5 Compatible with Miura AutoAnalyser & Semi Auto analyzers, reagents should be in 1 ml single test vial |
149 | CALCIUM - OCPC ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Reagents. OCPC Colorimetric 570 nm Endpoint Method. Linearity = 15 mg/dL Sensitivity = 0.2mg/dL CV < 2 % Standard : 8.0mg /d L. Compatible with Miura Fully Auto + Semi Auto Analysers. About 500 - 1000 ml. Packs. |
150 | Serum PHOSPHORUS Estimation Kit based on Phospho-Molybdate UV End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use single Reagent. UV End Point 340 nm Method. Standard : 5 mg% , Linearity : 15 mg/dL Sensitivity = 1 mg/dL. Compatible with Miura Fully Auto + Semi Auto Analysers. Long expiry date & stability. |
151 | Serum CHLORIDE Estimation Kit based on Mercuric Thiocyanate Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagent should be stabilized liquid form 2. To be supplied with chloride standard: 100 mEq/L 3. Linearity not less than 150 mEq/L |
152 | Serum MAGNESIUM Estimation Kit based on Xylidyl Blue Colorimetric End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Single Reagent. Colorimetric 570 nm End Point Method. Calmagite / Arsenazo I Standard : 2 mg/dL Calibrated. Linearity : 5 mg/dL Compatible with Miura Fully Auto + Semi Auto Analysers. |
153 | Serum BICARBONATE Estimation Kit based on Colorimetric UV End Point/Fixed Time Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagent should be stabilized liquid form or lyophilized powder with buffer for reconstitution provided 2. Reconstituted working reagent stability: at least 1 week at 2-8 degree C 3. Provided with bicarbonate standard of 20 or 25 mmol/L 4. Linearity not less than 50 mmol/L |
154 | Serum ALPHA(a) AMYLASE Estimation Kit based on Enzymatic Kinetic (IFCC) Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Single Reagent. Enzymatic - Kinetic 405 nm Method. Incubation : Only 1 Min. 37" C EPS / CNPG3 Substrate Linearity = 2000 U/L. Compatible with Miura AutoAnalyser & Semi Auto analyzers. long expiry date & stability |
155 | Serum LIPASE Estimation Kit based on Enzymatic Kinetic (IFCC) Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Lypholysed Stable Reagents. 550 nm Enzymatic -Colorimetric Method. Incubation : 10 Min. Substrate+ Activator + Buffer & Calibrator in Kit. Working reagent to have reconstituted Stability : 21 days. Linearity = 600 U/L Calibrator must be given with kit.Compatible with Miura Fully Auto + Semi Auto Analysers. |
156 | Serum Uric Acid estimation Kit based on Uricase-POD End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Reagents. Enzymatic End Point 500 nm Method. Incubation : 5 Minutes. Uricase> 200 U/L, Standard : 6 mg%, Linearity :20 mg% Sensitivity = 0.1 mg/dL. %CV=2. Compatible with Miura Fully Auto + Semi Auto Analysers. |
157 | Micro protein estimation Kit for determination of protein in urine & CSF based on Pyrogallol Red End-point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagent should be stabilized liquid form, ready to use. 2. To be supplied with standard of microprotein or calibrator. 3. Linearity at least 1000 mg/dL 4. Incubation up to 10 min maximum.5. Endpoint colour stability: at least 60 minutes. |
158 | Serum Fructosamine estimation kit based on NBT Kinetic Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Stable Lypholysed Reagents with buffer IFCC Kinetic 550 nm Method. Incubation : 5 Min. Working Reagent Onboard Stability = 30 days. Proteinase-K & Ketoamine Oxidase. Linearity upto 10 mMol/L 1 x 2 mL Liquid Calibrator & 2 x 1 mL Liquid Controls having open bottle stability of 30 days must be given with Kit. Compatible with Miura Fully Auto + Semi Auto Analysers. About 100 ml. Packs. |
159 | Serum Total Iron estimation kit based on Ferrozine Colorimetric End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagents are liquid stable ready to use or powder or tablets with buffer for reconstitution provided 2. Stability of the reconstituted reagent at least 4 weeks at 2 to 8 degree C. 1 or 2 mL reconstitution possible at a time. 3. Provided with iron standard of 1mg/L (100µg/dL) 5mL standard to be provided every 20 mL of reagent 4. Linearity not less than 800 µg/dL |
160 | Serum Copper estimation kit based on Colorimetric End Point Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. Colorimetric End Point Method. Reagents : 3,5,Di Br PAESA , Ascorbic acid and Calibrated. Standard of 100 microgram / dL Incubation : 5 Minutes. Linearity : 500 microgram/dL. Compatible with Miura Fully Auto + Semi Auto Analysers. |
161 | HDL-LDL Cholesterol Calibrator (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Lyophilized calibrator for HDL and LDL cholesterol 2. Reconstitution stability of at least 1 week at 2 to 8 degree C and at least 4 weeks at -20 degree C |
162 | CK-MB Calibrator (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Lyophilized calibrator for CK-MB 2. Reconstitution stability of at least 1 week at 2 to 8 degree C 3. Provided with method specific values |
163 | CK-MB Control Set (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Set of quality control sera of two different levels for CK-MB 2. Reconstitution stability of at least 1 week at 2 to 8 degree °C 3. Provided with method specific values. |
164 | Bilirubin Standard (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Aqueous bilirubin standard based on human/bovine serum for total and direct bilirubin assay standardization 2. Stable for at least 1 week after opening the bottles at 2 to 8 degree C when stored in dark |
165 | Bilirubin Standards Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Kit containing 3 to 5 levels of total and direct bilirubin standards intended for calibration verification, method evaluation and linearity check 2. Stable for at least 1 week after opening the bottles at 2 to 8 degree C when stored in dark. Kit containing 2 x 5 levels x 5 ml Combined Reference Material for Total Bilirubin and Direct Bilirubin to eneble Calibration, Linearity Checks, Method evaluation & Recovery studies. Adaptable to Miura Fully Autoanalyzer & Semi-Autoanalyzer. |
166 | Chemistry Standards Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Kit containing 3 to 5 levels of combined reference material for glucose, urea, creatinine, triglycerides, potassium, sodium & chloride in aqueous matrix for calibration verification, method evaluation and linearity check 2. Stable for at least 6 months after opening the bottles when stored as per manufacturer’s instructions |
167 | Blood Gas Controls – Pack of Normal and Abnormal level (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Multilevel Multianalyte blood gas controls containing pO2, pCO2, pH, sodium, potassium, ionized calcium 2. Stable till expiry at 2 to 8 degree C 3. Provided with method and instrument specific values |
168 | Blood Gas Controls –Abnormal level (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Multianalyte blood gas controls containing pO2, pCO2, pH, sodium, potassium, ionized calcium 2. Stable till expiry at 2 to 8 degree C 3. Provided with method and instrument specific values |
169 | Fructosamine Calibrator (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Lyophilized calibrator for fructosamine 2. Reconstitution stability of at least 1 week at 2 to 8 degree C 3. Provided with method specific values |
170 | Sampling Precision Test Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Kit for checking proper functioning of the sample fluid metering and photometric measuring system 2. Provided with detailed literature and/or software for calculation of sampling precision |
171 | Reagent Precision Test Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Kit for checking proper functioning of the reagent fluid metering and photometric measuring system 2. Provided with detailed literature and/or software for calculation of reagent precision |
172 | Quality Control Serum (Normal Level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature ) | 1. The product must be multi-analyte normal level quality control serum prepared from pooled human sera and intended for verification of precision of clinical chemistry assays suitable for automated analyzers and manual procedures. 2. It should contain all routinely measured parameters and hormones i.e. Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH 3. The quality control sera must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 4. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 5. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 6. Company should have ISO certificate. 7. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests. |
173 | Quality Control Serum (Pathological- Higher level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature ) | 1. The product must be multi-analyte pathological (high level) quality control serum prepared from pooled human sera and intended for verification of precision and accuracy of clinical chemistry assays suitable for automated analyzers and manual procedures. 2. It should contain all routinely measured parameters and hormones i.e. Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH. 3. The quality control sera must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 4. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 5. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 6. Company should have ISO certificate. 7. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached.8. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests. |
174 | Quality Control Serum (Pathological- Lower level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature ) | 1. The product must be multi-analyte lower level quality control serum prepared from pooled human sera and intended for verification of precision and accuracy of clinical chemistry assays suitable for automated analyzers and manual procedures. 2. It should contain all routinely measured parameters. 3. The quality control sera must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 4. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 5. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 6. Company should have ISO certificate. 7. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached. 8. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests. |
175 | Multicalibrator Sera for Clinical Chemistry Assays (Normal Level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature) | 1. The product must be Normal level multicalibration serum intended for calibration of clinical chemistry assays suitable for automated analyzers and manual procedures. Calibrator sera should contain all routinely measured parameters. It must contain the following parameters: Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH 2. The calibrator must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 3. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 4. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 5. Company should have ISO certificate. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached. 6. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests. |
176 | Multicalibrator Sera for Clinical Chemistry Assays (Higher Level) (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature) | 1. The product must be Higher Level multicalibration serum intended for calibration of clinical chemistry assays suitable for automated analyzers and manual procedures.Calibrator sera should contain all routinely measured parameters. It must contain the following parameters: Glucose, Urea, Creatinine, SGOT, SGPT, Alkaline Phosphatase, Sodium, Potassium, Total Calcium, Bicarbonate/Total CO2, Total Bilirubin, Direct Bilirubin, Total Protein, Albumin, Total Cholesterol, HDL, LDL, Triglycerides, CK, T3, T4, TSH 2. The calibrator must be lyophilised human serum based product. The chemicals and biological components included in the product must act in the serum matrix in a similar manner to the corresponding components found in human sera. The calibrator should be provided with diluent for reconstitution if applicable. 3. Analyte concentration should be stable for at least 5 days in reconstituted product at 2 to 8oC; and for not less than 1 month when frozen. 4. The product should be supplied with detailed literature consisting of method of using the product and values of individual analytes specific for instruments available in the Clinical Chemistry Laboratory. 5. Company should have ISO certificate. Supplied calibrator sera should be preferably approved by FDA – USA / equivalent foreign/Indian institution. Copy of certificate should be attached. 6. The product must be free of known infectious agents/viruses and must have been proven non-reactive in relevant tests. |
177 | Multi-parameter External Quality Assessment Scheme for Routine Clinical Chemistry Investigations (Vendor must provide Application Sheets / MSDS and Protocol for use of material. Temperature, Instrument and Method Specific Data, Values for all tests in User Menu. Quote the Cost per mL of the Reconstituted Liquid Material and Pack Size. Manufacturer must have all quality certifications ISO 13485 + CE mark + US.FDA Attach complete Kit Literature) | 1.It should a well recognized scheme having large number of participants and effective consolidated programme having once monthly or once biweekly sample frequency. 2. The samples provided should be lyophilized human serum samples.3. The analyte values in the sample should cover clinically relevant ranges to test accuracy and precision of the reported results. 4.The scheme must deliver regular reports in user friendly format with rapid turnaround. 5. The results must include reference method results as well as results for instruments and methods used by participating laboratory and other routine methods. 6. The results should help identify trends, biases and precision problems using appropriate statistical data and graphs. 7. The participating laboratory should have access to advisory panel to troubleshoot any technical queries and to get advice regarding corrective actions. 8. The scheme must provide certificate of participation at the end of the cycle. 9. The EQA scheme system must be ISO/IEC certified |
178 | AMMONIA ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable / Lypholysed Reagents. UV - End Point Method. NADPH > 0.25mmol/L GLDH>1000U/L. Standard: 0.5 mg% Linearity : 2 mg% Compatible with Miura Fully Auto + Semi Auto Analysers. About 100 ml. Packs |
179 | C - Reactive Protein Calibrator Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid ready use calibrator having 30 days open bottle stability when stored at 2-8*C, Adaptable to MiuraFully Autoanalyzer. 5 x 2 mL packs |
180 | C - Reactive Protein Control Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Kit containing liquid control solutions Level-1 and Level -2 for High sensitivity CRP Immunoturbidimetric Estimation Kit. Open bottle atability of 30 days at 2 - 8*C.Adaptable to Miura Autoanalyzer.2 x 3 mL packs |
181 | CHOLINESTERASE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. Enzymatic - Kinetic Method. DTNB , Butyryl thiocholine substrate Linearity > 6000 U / L Compatible with MiuraFully Auto + Semi Auto Analyser. About 50 ml. Packs. |
182 | G6 PDH ESTIMATION KIT (QUANTITATIVE) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable R1, R2, R3 Ready use Reagents. Enzymatic Kinetic 340 nm Method. Incubation : Only 5 Minutes. Cholesterol Oxidase > 180 U / L Compatible with Miura Fully Auto + SemiAuto Analyser. About 50 - 100 Test Packs. |
183 | Immunoturbidi metric Kit for HbA1C (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Kit containing Ready use, liquid stable reagents R1, R2 & R3 having linearity upto 15 gm %, Immunoturbidimetric 660 nm photometric method. Adaptable on Miura FullyAuto analyzer & semi auto analyzer, with controls level 1 and 2, calibrator |
184 | HbA1C Calibrator Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Lyophilised calibrators having reconstitution stability of minimum 30 days at 2-8*C Adaptable to Miura Fully Autoanalyzer. 4 x 0.5 mL packs. |
185 | HbA1C Control Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Set of Controls Level 1 & Level 2 having reconstitution stability of minimum 30 days at 2-8*C Adaptable to Miura Fully Autoanalyzer. 2 x 0.5 mL packs |
186 | Hemolysis Reagent for Immunoturbidi metric HbA1C Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Kit containing Ready use, liquid stable reagent for Total HbA1C Immunoturbidimetric estimation. |
187 | Homocysteine Calibrator Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid ready use calibrators having long stability when stored at 2-8*C, Adaptable to Semi-Auto & Miura Fully Autoanalyzer. 2 x 2 x 3 mL packs |
188 | HOMOCYSTEINE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Reagents. R1, R2, R3. Enzymatic UV Kinetic 340 nm Method. Calibrators must be supplied with Kit having reconsituted open bottle stability of 30 days.Linearity 50 umol / L. Compatible with MiuraFully Auto + Semi Auto Analysers. 50 - 100 mL Packs. |
189 | IgA. Immunoglobulin A ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable / Lypholysed Reagents. Immunoturbidimetric UV-Manual Method. Incubation : 5 Minutes. Anti IgA antibody (human) Calibrator/ Controls with kit. Compatible with Miura Fully Automated Analyser. About 50 ml. Packs. |
190 | IgG. Immunoglobulin G ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable / Lyophilised Reagents. Immunoturbidimetric UV-Manual Method. Incubation : 5 Minutes. Anti IgG antibody (human) Calibrator / Controls with kit. Compatible with Miura Fully Automated Analysers. About 50 ml. Packs. |
191 | IgM. Immunoglobulin M ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable / Lyophilysed Reagents. Immunoturbidimetric UV-Manual Method. Incubation : 5 Minutes. Anti IgM antibody (human) Calibrator or Controls with kit. Compatible with Miura Fully Automated Analysers. About 50 ml. Packs. |
192 | Immunoturbidi metric Kit for C -Reactive Protein (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Kit containing liquid stable reagents R1 & R2 having linearity of 0.1 - 300 mg / dL High sensitivity CRP Antibody / Latex Turbidity, 570 nm photometric method. Adaptable on Miura FullyAutoanalyzer |
193 | Immunoturbidi metric Kit for Microalbumin (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Kit containing liquid stable reagents R1 & R2 having linearity of 0.5 - 30 mg / dL, 340 / 700 nm photometric method. Adaptable on Miura FullyAutoanalyzer |
194 | Immunoturbidi metric Kit for Pre Albumin (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Kit containing ready use liquid stable reagents R1 & R2 having linearity upto 60 mg / dL, Immunoturbidimetric 340 / 700 nm photometric method. Adaptable on Miura Fully Autoanalyzer |
195 | IRON ( TOTAL ) ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. 630 nm Chromazurol - End Point Method. Incubation : Only 5 Min. Chromazurol : 2 mmol/L Standard : 1mg/L , Linearity : 5 mg/L Compatible with Miura Fully Auto + Semi Auto Analysers. About 200 - 500 ml. Packs. |
196 | LACTATE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. Enzymatic - End Point Method. Incubation : Only 5 Minutes. Peroxidase>1800 U/L , Standard : 40 mg/dL Linearity : 100 mg / dL. Compatible with Miura Fully Auto + Semi Auto Analysers. About 100 ml. Packs. |
197 | MICRO-ALBUMIN ( Micro-Protein ) IN CSF / SERUM / URINE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready use Single Reagents. Colorimetric End Point 600 nm Method. Pyrogallol red : 0.06 mmol / L Standard : 50 mg % Sensitivity 10 mg/dL. %CV=1.5 Calibrator & Controls Level 1& 2 having 6 months open bottle stability with Kit. Linearity : 200 mg % Compatible with Miura Fully Auto + Semi Auto Analysers. About 500 ml. Packs. |
198 | Micro-Albumin Calibrator Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid ready use Liquid calibrators having stability of minimum 30 days at 2 - 8*C Adaptable to Miura Fully Autoanalyzer. 6 x 1 mL packs |
199 | Micro-Albumin Controls Set Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid ready use Liquid calibrators having stability of minimum 30 days at 2 - 8*C Adaptable to Miura Fully Autoanalyzer. 6 x 1 mL packs |
200 | PANCREATIC ALPHA AMYLASE ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. Antibody-Enzymatic Kinetic Method. Incubation : Only 5 Min. Substrate : Ethylidene G7pNP Glucosidase >20 U/L Linearity : 1500 U/L. Compatible with Miura Fully Auto + Semi Auto Analysers. 100 mL Packs |
201 | Serum Cystatin -C Estimation Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagent Kit. Photometric Assay. Adaptable to Miura Autoanalyzer. Shelf life = 1 year and on board stability of opened reagent should be atleast 14 days. Kit must contain Calibrators & QC material |
202 | HbA1c Estimation kit for Fully Automated Biochemistry Analyzer (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagents are liquid stable ready to use 2. Provided with HbA1c calibrator 3. Sensitivity: 0.3 gm/dL or better 4. Linearity: 2.5 gm/dL or better (or up to 15%) |
203 | HbA1c estimation kit based on affinity chromatography Method (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. Reagents are liquid stable ready to use or powder or tablets with buffer for reconstitution provided 2. Provided with HbA1c calibrator 3. Detection range: 3% to 15% or wider |
204 | Serum Ferritin kit (Latex Turbidimetry Method) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1x40 ml R1 Diluent, 1x10 ml R2 Latex, 1x3 ml FERR-CAL |
205 | Total Iron Standard Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Kit containing 5 x 15 ml Combined Reference Material for Total Iron & Ammonia to eneble Calibration, Linearity Checks, Method evaluation & Recovery studies. Adaptable to Miura Fully Autoanalyzer. |
206 | UIBC ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Ready Use Reagents. Ferrozine EndPoint 560 nm method. Linearity upto 500 ugm/dL Adaptable to Miura Autoanalyzer & Semi-Auto analysers. 200 - 500 mL packs. |
207 | ZINC ESTIMATION KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Liquid Stable Reagents. Colorimetric Method. Chelation with 5-Br-PAPS. Standard of 200 micrograms. Linearity : 1000 micrograms. Incubation : 5 Min. Compatible with MiuraFully Auto + semi Auto Analysers. About 100 mL Packs |
208 | HDL / LDL Cholesterol Control Kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Lyophilised combined reagent having reconstitution stability of minimum 7 days at 2-8*C Adaptable to Miura Fully Autoanalyzer. 10 x 3 mL packs |
209 | Rapid Troponin-I Card Test (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. One step rapid chromatographic immunoassay for detection of troponin-I in whole blood or serum 2. Read time not more than 15 minutes 3. Sensitivity 1ng/mL or better 4. Sample volume required 200µL or less 5. Each cassette provided with dropper 6. Stable at room temperature till expiry |
210 | Cassette for detection of Acute Myocardial Infarction (Troponin-I, CK-MB and Myoglobin) (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. One step rapid chromatographic immunoassay for detection of troponin-I, CK-MB and Myoglobin in whole blood or serum 2. Read time not more than 15 minutes 3. Sensitivity: Troponin-I : 1ng/mL or better CK-MB : 5 ng/mL or better Myoglobin : 100 ng/mL or better 4. Sample volume required 300µL or less 5. Each cassette provided with dropper 6. Stable at room temperature till expiry |
211 | Serum T3 (Triiodothyronine) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. ELISA kit for quantitative determination of T3 in human serum containing 96 well antibody coated microtitre plate, ready to use T3 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.1 ng/mL or lower 4. Opened kit stable till expiry date when stored as per manufacture instructionsEnclose all details of Composition, CV & Precision data of Kit. |
212 | Serum Free T3 (Free Triiodothyronine) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | 1. ELISA kit for quantitative determination of T3 in human serum containing 96 well antibody coated microtitre plate, ready to use T3 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.07 pg/mL or lower 4. Opened kit stable till expiry date when stored as per manufactures instructionsEnclose all details of Composition, CV & Precision data of Kit. |
213 | Serum T4 (Thyroxin) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of T4 in human serum containing 96 well antibody coated microtitre plate, ready to use T4 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 10 nmol/L or lower 4. Opened kit stable till expiry date when stored as per manufactures instructionsEnclose all details of Composition, CV & Precision data of Kit. |
214 | Serum Free T4 (Free Thyroxin) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of T4 in human serum containing 96 well antibody coated microtitre plate, ready to use T4 reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.08 ng/dL or lower |
215 | Serum TSH (Thyroid Stimulating Hormone) Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer. ELISA kit for quantitative determination of TSH in human serum containing 96 well antibody coated microtitre plate, ready to use TSH reference standards of at least 6 levels and necessary reagents and buffers 2. 450nm procedure 3. Minimum detectable concentration: 0.1 mIU/mL or lower 4. Opened kit stable till expiry date when stored as per manufactures instructionsEnclose all details of Composition, CV & Precision data of Kit. |
216 | Preventive maintenance (PM) kit for Erba CHEM 5 Plus V2 semiauto-analyzer (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Preventive maintenance (PM) kit for Transasia Erba CHEM 5 Plus V2 semiauto-analyzer |
217 | Serum Anti-TPO Antibodies Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ).Streptavidin Biotin Based Sandwich Assay 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
218 | Serum CA-19.9 Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
219 | Serum Alpha Feto Protein Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
220 | Serum beta-HCG Estimation Elisa kit (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
221 | Serum PSA Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
222 | Serum CEA Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
223 | Serum FSH Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
224 | Serum LH Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
225 | MULTI ASSAY HUMAN SERA BASED TUMOUR MARKER CONTROLS KIT FOR LABORATORY Q.C. (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer. LEVEL I & II (Normal & pathological) |
226 | Serum CA-125 Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of CA 125 in human serum containing 96 well antibody coated microtitre plate, ready to use CA 125 reference standards of at least 6 levels and necessary reagents and buffers . 450nm procedure |
227 | Serum Adiponectin Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of adiponectin in human serum containing 96 well antibody coated microtitre plate, ready to use adiponectin reference standards of at least 6 levels and necessary reagents and buffers . 450nm procedure . sensitivity of < 25 pg/ml. sample volume less than 100 µL |
228 | Serum Leptin Estimation Kit based on ELISA (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.ELISA kit for quantitative determination of leptin in human serum containing 96 well antibody coated microtitre plate, ready to use leptin reference standards of at least 6 levels and necessary reagents and buffers . 450nm procedure . sensitivity of < 3.5 pg/ml. sample volume less than 100 µL |
229 | Serum CA-15.3 Estimation ELISA KIT (Attach complete Kit Literature with Valid ISO 13485 & CE Mark or US.FDA Certificate of Kit Manufacturer ) | Compatible with ELISA Reader and Washer.Coated Microwell Enzyme Immuno - Assay ( EIA ) 450 nm read method. Enz-antibody Conjugate & biotinylated monoclonal antibody, Substrate-TMB, Buffer & Stop Solution. Must have Six 1 mL Serum Reference Standards. with control level I and II. Enclose all details of Composition, CV & Precision data of Kit. Stability : 60 days. Packs : 96 Tests. |
230 | Bees wax | As per Column no.2 |
231 | TLE 1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
232 | PDL 1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
233 | PAX 5 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
234 | DOG-1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
235 | STAT6 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
236 | NUT | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
237 | MUC 1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
238 | MUC5AC | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
239 | MUC6 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
240 | MUC4 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
241 | TFE3B | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
242 | B72.3 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
243 | BCL10 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
244 | BCL6 Oncoprotein | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
245 | Beta-Amyloid | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
246 | BG-8 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
247 | CA19-9 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
248 | Cathepsin B | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
249 | CD3 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
250 | CD103 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
251 | Cd11c | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
252 | CD123 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
253 | CD13 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
254 | CD138 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
255 | CD14 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
256 | CD19 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
257 | CD1a | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
258 | CD2 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
259 | CD22 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
260 | CD23 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
261 | CD24 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
262 | CD25 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
263 | CD33 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
264 | CD36 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
265 | CD38 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
266 | CD3-epsilon chain | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
267 | CD4 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
268 | CD43 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
269 | CD45 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
270 | CD45RA | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
271 | CD45RO | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
272 | CD61 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
273 | CD64 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
274 | CD7 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
275 | CD71 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
276 | CD9 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
277 | Collagen IV | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
278 | Cytokerain18 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
279 | D2-40 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
280 | EBER | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
281 | EBV | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
282 | EGFR | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
283 | Epstein barr virus early antigen | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
284 | Epstein-Barr Virus(LMP) | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
285 | F13a | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
286 | F8 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
287 | FL1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
288 | GH | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
289 | Glucagon | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
290 | Glycophorin A | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
291 | Growth hormone | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
292 | HBME-1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
293 | HbsAg | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
294 | Hemoglobin A | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
295 | HIV,p24 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
296 | HLADR | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
297 | IgA,Specific for Alpha-Chains | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
298 | IgG,Specific for gamma chains | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
299 | IgM,specific for Mu-chains | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
300 | IMP3 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
301 | INI 1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
302 | Insulin | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
303 | J chain | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
304 | Kappa light chains | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
305 | Lambda light chains | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
306 | Mammaglobin | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
307 | Mast cell tryptase | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
308 | MITF | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
309 | MOC-31 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
310 | MUC2 Protein | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
311 | MUM1 Protein | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
312 | Myelin Basic Protein | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
313 | MyoD1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
314 | NapsinA | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
315 | NESTIN | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
316 | OCT--4 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
317 | PAP(Prostatic acid phosphatase) | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
318 | P 16 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
319 | PCNA | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
320 | PE-10 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
321 | Plasma cell (Clone Vs38c) | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
322 | PP | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
323 | PR | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
324 | PTEN | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
325 | PTH | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
326 | RCC | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
327 | S-100 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
328 | Somatostatin | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
329 | TIA-1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
330 | TRAP | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
331 | Tryptase | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
332 | NKX3.1 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
333 | EZ-Dewax solution | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
334 | Alpha - 1 - Antitrypsin | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
335 | Alpha - 1 - Antichymotrypsin | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
336 | CD 13 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
337 | CD 14 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
338 | CD 16 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
339 | CDw 75 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
340 | CK 5 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
341 | CK8 & 18 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
342 | CK 14 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
343 | CK 15 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
344 | CK 16 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
345 | CK 17 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
346 | CK 18 | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
347 | WT 1(Antibody to carboxy terminal) | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
348 | Epcam | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
349 | Factor VIII related antigen | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
350 | Factor XIII A | Antibodies (IMMUNOHISTOCHEMISTRY ITEM) Ready to use |
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