Request For Quotation Laboratory Consumables/Gratkhanalyk Shygyn Material

Urea 10505. Kinetic Test For Determining Urea In Serum, Plasma And Urine Urea Liquicolor Packing 2X100 Ml. Method. Urea Is Hydrolyzed In The Presence Of Water And Urease With The Formation Of Ammonia And Carbon Dioxide. In The Modified Reaction Of Bertelot, Ammonia Ions React With Hypochlorite And Salicylate With The Formation Of Green. An Increase In Absorption At 578 Nm Is Proportional To The Concentration Of Urea In The Examined Sample. Reagent 1 Phosphate Buffer (Ph 7.0) 120 Mmol/L Salicilate Sodium 60 Mmol/L Nitroprusside Sodium 5 Mmol/L Edta 1 Mmol/L Reagent 2. Phosphate Buffer (Ph <13) 120 Mmol/L Hypochlorite ≈ 0 Urea Standard 3 Ml Of Urea Equivalent To Bun 37.28 Mg/Dl Or 6.2 Mmol/L Azid Sodium 0.095 % Stability Of Reagents. The Reagents Are Stable Before Their Expiration Date, Provided That They Are Stored In A Sealed Form At A Temperature Of 2 ... 8 ° C. [Rgt1], [Rgt2] And [Enz] After Opening Are Stable For 6 Weeks, Provided That They Are Stored At A Temperature Of 2 ... 8 ° C Or 2 Weeks At 15 ... 25 ° C. The Standard Is Stable Before The Expiration Of The Expiration Date, Even After The Opening. Enzyme Reagent 1A Is Stable For 4 Weeks At A Temperature Of 2 ... 8 ° C Or 2 Weeks At A Temperature Of 15 ... 25 ° C., Cholesterol 10017. A Set Of Reagents For Determining Cholesterol In Serum Or Blood Plasma “Cholesterol Liquicolor” Packing 4 X 30 Ml Method Of Cholesterol Is Determined After Enzymatic Hydrolysis And Oxidation. The Hydrogen Peroxide Formed As A Result Of These Reactions Interacts Under The Influence Of Peroxidase With 4-Aminoantypio And Phenol With The Formation Of A Painted Product- Chinonine An Enzymatic Reagent Phosphate Buffer (Ph 6.5) 100 Mmol/L 4- Aminoantilin 0.25 Mmol/L Phenol/L Peroxidase> 5000 E/L Cholesteringallase> 150 E/L Cholesterinsidase> 100 E/L Azid Sodium> 0.05% Std - A Standard Cholesterol Solution 200 Mg/Dl Or 5.17 Mmol/L Samples Of Serum Or Plasma Treated With Heparin Or Edta. Measurement Conditions Of The Wavelength Of 500 Nm, Hg 546 Nm Optical Path 1 Cm Temperature 20Os-25Os Or 37Os Measurement Against The Idle Test Along The Reagent. We Need One Idle Test For The Series., Calibration Solutions: Humatrol P 6X5 Ml. Humatrol P Is A Serum To Control The Quality Of Clinical Biochemical Studies. Each Set Contains A Reagent In The Amount Of 6Í5.0 Ml To Perform Diagnostic Studies In Vitro Ivd. Ref Lamp 13512. Humatrol P Liophilizate Catalog Number, Alkaline Phosphatase 12017. Colorimetric Test For Determining Alkaline Phosphotase In Serum And Blood Plasma Alkaline Phosphatase Liquicolor Packing 10X10 Ml., Alat 12011. Liquid -Uf Test Determining The Activity Of Alaninaminotransferase - Alat In Serum And Blood Plasma Gpt (Alat) Ifcc Mod. Liquiuv Humazym Test ”, Packing 10X10ml No More, R1- Reagent 1, Enzymatic Reagent Tris Buffer (Ph 7.5) -100 Mmol/L L-Alanin- 500 Mmol/L. Lactate Dehydeghenase (Ldh)> 1200 E/L R2 - Reagent 2, Starting Reagent 2 -Oxoglurat 15 Mmol/L Nadh 0.18 Mmol/L. Samples. Serum Or Plasma Treated With Heparin Or Edt Plasma. Do Not Allow Hemolysis! The Loss Of Activity In 3 Days Is: At +4 ° ~ 10%, At 20-25 ° C-17% Of The Measurement Condition. The Wavelength Of Hg 365 Nm, 340Nm Or Hg 334 Nm Optical Path 1 Cm Temperature 25 ° C, 30 ° C Or 37 ° C. Measurement: Against Air (Or Dist. Water), Reaction With A Decrease In The Optical Density Of Calculation Of The Calculation Of The Change In The Wholesale. Density In 1 Minute (Da/Min) In The Range Of 0.06-0.08 (Hg 365 Nm) Or 0.12-0.16 (Hg 334 Nm, 340 Nm) (Procedures 1+2), Use Only The Results Of The First 2 Minutes (1 Minute Of Incubation, 2 Minutes Of Measurement)., Asat 12011. Liquid -Uf Test Determining The Activity Of Alaninaminotransferase - Assat In Serum And Blood Plasma Gpt (Asat) Ifcc Mod. Liquiuv Humazym Test ”, Packing 10X10ml No More, R1- Reagent 1, Enzymatic Reagent Tris Buffer (Ph 7.5) -100 Mmol/L L-Alanin- 500 Mmol/L. Lactate Dehydeghenase (Ldh)> 1200 E/L R2 - Reagent 2, Starting Reagent 2 -Oxoglurat 15 Mmol/L Nadh 0.18 Mmol/L. Samples. Serum Or Plasma Treated With Heparin Or Edt Plasma. Do Not Allow Hemolysis! The Loss Of Activity In 3 Days Is: At +4 ° ~ 10%, At 20-25 ° C-17% Of The Measurement Condition. The Wavelength Of Hg 365 Nm, 340Nm Or Hg 334 Nm Optical Path 1 Cm Temperature 25 ° C, 30 ° C Or 37 ° C. Measurement: Against Air (Or Dist. Water), Reaction With A Decrease In The Optical Density Of Calculation Of The Calculation Of The Change In The Wholesale. Density In 1 Minute (Da/Min) In The Range Of 0.06-0.08 (Hg 365 Nm) Or 0.12-0.16 (Hg 334 Nm, 340 Nm) (Procedures 1+2), Use Only The Results Of The First 2 Minutes (1 Minute Of Incubation, 2 Minutes Of Measurement)., Bilirubin 10740. Bilirubin D+T Test - Bilirubin Straight/General, Full Test Set, 2X100 Ml Of Indirect Bilirubin Is Released Under The Influence Of The Detergent. Bilirubin Is Direct/General, Interacts With The Diazocomplex Of 3.5-Dichlorophenil-Diazonium-Tetrafluorobortic (Dpd) With The Formation Of A Nibilirubin. The Value Of The Optical Density Of The Azobilirubin At 546 Nm Is Directly Proportional To The Concentration Of The Total Bilirubin In The Rgt 1 Sample. Detergent (Green Cover) 3.5-Dichlorophenil-Diazonium-Tetrafluoroboratt 0.9 Mmol/L Caffeine 5.2 Mmol/L Lid) To Determine The General Bilirubin Nitrite Sodium 390 Mmol/L, Preparation And Stability Of Reagents. Reagents Are Ready For Use. Before Opening, The Reagents Are Stable Up To The Specified Date At Storage Temperature 2 ... 8 ° C. After Opening, The Reagents Retain Stability For 30 Days When Storing The “On Board” Of The Analyzer At 2 ... 12 ° C. The Coloring Reagent Should Be Protected From Light. Serum, Heparinized Plasma. Avoid Hemolysis! Samples Must Be Protected From Light. Bilirubin In A Sample Is Stable When Stored In A Place Protected From Light For 3 Days At A Temperature Of 2 ... 8 ° C Or 3 Months At –20 ° C. Measurement Conditions. The Wavelength Of 546 Nm (520-560 Nm) Is An Optical Path Of 1 Cm Temperature Of 20 ° C Or 37 ° ° C To A Single Test Along The Reagent, A Reaction With An Increase In Optical Density., The Total Protein 157004. A Photometric Colorimetric Test For Determining The Total Protein By The Burea Method In Serum Or Blood Plasma “Total Protein Liquicolor” Packing Of 1000 Ml Of Copper Iona Is Reacted With Protein In An Alkaline Solution With The Formation Of A Violet Complex. The Absorption Of This Complex Is Proportional To The Concentration Of Protein In The Studied Sample Color Codroxide Sodium 200 Mmol/L Tartrap Potassium And Sodium 32 Mmol/L Sulfate Copali 30 Mmol/L Iodide Of Potassium 30 Mmol/L Standard Protein 8 G/Dl Or 80 G/L Azid Sodium 0.095%., Glucose 10260. An Enzymatic Colorimetric Test For Determining Glucose Without Depropetheinization In Serum And Blood Plasma “Glucose Liquicolor” Packing 4X100 Ml Is No Less Than The Method: Glucose Is Enzymaticly Oxidized In The Presence Of Glucoseoxidase. The Hydrogen Peroxide Formed In The Reaction Process Reacts In The Presence Of Peroxidase With Phenol And 4-Aminophenazone And Forms A Red-Violet Chinon-Imin Product That Is Fotomethy. Enzymatic Reagent Phosphate Buffer (Ph 7.5) 0.1 Mol/L 4-Aminophenazone 0.25 Mmol/L Phenol 0.75 Mmol/L Glucose Oxidase (Go)> 15 Kep/L Peroxidase (N) 1.5 Kep/L Mutarotase> 2.0 Kep/L Stabilizers Of The Deproteinizing Solution Of Uraceuity 1.6 G/L Sodium Chloride 9 G/L, The Stability Of Reagents Are Stable Up To The Specified Date (Exp. Date) At Storage Temperature 2..8ºс. After Opening The Bottles, Avoid Bacterial Infection Of Reagents. An Enzyme Reagent Is Stable For 2 Weeks At A Temperature Of 15-25ºс. The Linearity Of The Reagent Test Is Lines To The Concentration Of Glucose 700 Mg/Dl Or 38.85 Mmol/L. If The Concentration Of Glucose In The Sample Exceeds The Specified Values, Dilute The Defosited Baise Fluid With A Defoster Solution In A Ratio Of 1: 1 And Repeat The Study. Multiply By 2 (Breeding Factor)., Ggt 12013. Colorimetric Test For Determining The Activity Of Gamma Glutamiltransferase In Serum And Blood Plasma “G-Gt Liquicolor Humazym Test” Packing 10X10 Ml., Calibration Solutions: Humatrol N 6X5 Ml Humatrol. N Is A Serum For Controlling The Quality Of Clinical Biochemical Studies Control. Each Set Contains A Reagent In The Amount Of 6Í5.0 Ml To Perform Diagnostic Set Of 1,39,850 Studies In Vitro Ivd. Ref Lamp 13511. Humatrol N Lio -Liolete, Prepared From Bull Serum With The Established Content Of All Important Components Of Human Serum., Creatinine 10051. The Kinetic Method Without Deproteinization For Measuring Creatinine In Serum, Plasma And Urine “Creatinine Liquicolor” Packaging 200 Ml Is No Less Complexity Of Sodium Hydroxide Xi, (R36/38) (S 26-37/39-45) 2 × 100 Ml Of At Least Picrinoic Acid 1 × 50 Ml Standard Createnin 1 × 5 Ml. The Scope Is Used In Clinical And Diagnostic Laboratories Of Medical Organizations And Is Intended For The Quantitative Determination Of Creatinine In Serum, Heparinized Plasma And Urine. The Principle Of Method1.2 Creatinine Interacts With Picrinic Acid In An Alkaline Environment With The Formation Of An Orange-Red Complex. The Optical Density Of The Formed Complex Is Proportional To The Concentration Of Creatinine In The Sample. Creatinine Reaction Scheme + Picrinic Acid ------> Creatinin-Pikrata Complex. The Stability Of The Reagents Are Stable Even After Opening The Packaging Up To The Specified Date Of Expiration Date [] If They Were Stored In A Closed Container At A Temperature Of [] From +15 ° C To +25 ° C. Contamination Of Reagents Should Be Avoided. The Working Reagent Retains Stability For 4 Weeks At A Temperature Of +15 ° C To +25 ° C In A Closed Container In A Place Protected From Light. Determination Of The Wavelength: Hg 492 Nm (490-510 Nm) Optical Path: 1Cm Temperature: +37 ° C Measurement: Against Air (Increasing Optical Density). Warm Up Reagents And Cuvettes To The Desired Temperature And Maintain It Constant (± 0.5 ° C) During The Test.