Request For Quotation Purchase Of A Reagent Kit And Medical Product For The Provision Of Paid Services

Antigen-B-Hbs Confirmatory Test A Set Of Reagents For Enzyme-Linked Immunosorbent Confirmation Of The Presence Of Hbsag In Serum And Blood Plasma, No Less Than 48 Od Per Set (6*8), Sensitivity No Less Than 0.5/0.01 Iu/Ml, D0558 Shelf Life No Less Than 24 Months, Physiological Solution Nacl 0.9% Not Less Than 400 Ml In A Bottle For Therapeutic Plasmapheresis, Medical Laboratory Tray Made Of Stainless Steel, Size No Less Than 18 Centimeters, Height No Less Than 2 Centimeters, Standard Panels Of Red Blood Cells For Antibody Screening Using The Gel Method On A Saxo Bio-Rad Apparatus. In A Package Of At Least 3 Bottles Of 10 Ml, One Package For At Least 100 Studies, Anti-Hcv - Strip Set Of Reagents For Enzyme Immunoassay Detection Of Immunoglobulins Of Classes G And M To The Hepatitis C Virus, 60X8, Indirect Elisa, Two-Stage Method. The Number Of Definitions Is At Least 480 (60X8). Possibility Of Spectrophotometric Control Of The Addition Of Samples And Reagents. The Minimum Analysis Time Is No More Than 1 Hour 30 Minutes. The Number Of Elisa Protocols Is At Least 2. The Calculation Of The Positivity Rate Is Provided. The Shelf Life At The Time Of Delivery Is At Least 80% Of The Standard. Fractional Use Of The Kit Can Be Realized Throughout The Shelf Life. Availability: Films For Sealing The Tablet, A Zip-Lock Bag For The Tablet, Trays For Reagents, Tips For Pipettes, Standardized Non-Specific Components Of Fsb-T, Stop Reagent, Registration Certificate. Possibility Of Transportation At Temperatures Up To 25ºс For At Least 9 Days. Contents Of The Kit: - Collapsible Tablet With Immobilized Recombinant Antigens Of The Hepatitis C Virus, Ready For Use - 1 Piece; - Positive Control Sample (K+) Based On Inactivated Human Blood Serum, Containing Antibodies To Hcv, Ready For Use - 1 Vial, 1 Ml; - Negative Control Sample (K–) For Based On Inactivated Human Blood Serum, Not Containing Antibodies To Hcv, Ready For Use - 1 Vial, 1 Ml; - Conjugate (A Mixture Of Antibodies To Human Igg And Igm, Labeled With Horseradish Peroxidase), Concentrate - 1 Vial, 1.5 Ml; - Solution For Diluting The Conjugate (Rc) - 1 Vial, 13 Ml; Solution For Diluting Serums (Rs) - 1 Vial, 10 Ml; - 25-Fold Concentrate Of Phosphate-Buffered Saline Solution With Tween (Fsb-T×25) - 1 Vial, 28 Ml; - Tetramethylbenzidine (Tmb), Concentrate - 1 Vial, 1.5 Ml; -Substrate Buffer Solution (Sbr) – 1 Fl., 13 Ml;  Stop Reagent, Ready For Use – 1 Vial, 12 Ml. The Set Is Additionally Equipped With: Films For Sealing The Tablet – 3 Pcs., Baths For The Reagent – ​​2 Pcs., Tips For Pipettes – 16 Pcs., Anti-Hcv Set Of Reagents For Enzyme Immunoassay Detection And Confirmation Of The Presence Of Immunoglobulins G And M To The Hepatitis C Virus, 48 ​​Samples, Indirect Elisa, Two-Stage Method, Number Of Determinations 48 (12X4). The Antigens Are Arranged Horizontally On The Plate: Core In Rows A, C, E, G; Ns In Rows B, D, F, H. Possibility Of Spectrophotometric Control Of The Addition Of Samples And Reagents. The Minimum Duration Of Analysis Is No More Than 1 Hour 30 Minutes. The Number Of Elisa Protocols Is At Least 2. The Calculation Of The Positivity Rate Is Provided. Availability: Film For Sealing The Tablet, A Zip-Lock Bag For The Tablet, Standardized Non-Specific Components Fsb-T, Stop Reagent, Registration Certificate. Possibility Of Transportation At Temperatures Up To 25ºс For At Least 9 Days. Composition: The Kit Includes: - A Collapsible Tablet With Immobilized Recombinant Antigens Of The Hepatitis C Virus, Ready For Use - 1 Pc.; - Positive Control Sample (K+) Based On Inactivated Human Blood Serum, Containing Antibodies To Hcv, Ready For Use – 1 Vial, 1.0 Ml; - Negative Control Sample (K–) Based On Inactivated Human Blood Serum, Not Containing Antibodies To Hcv, Ready For Use – 1 Vial, 1.0 Ml; - Conjugate (A Mixture Of Antibodies To Human Igg And Igm Labeled With Horseradish Peroxidase), Concentrate – 1 Vial, 1.5 Ml; - Solution For Diluting The Conjugate (Rc) – 1 Vial, 13.0 Ml; - Serum Dilution Solution (Rs) – 1 Vial, 10.0 Ml; - Tetramethylbenzidine (Tmb), Concentrate – 1 Vial, 1.5 Ml; - Substrate Buffer Solution (Sbr) – 1 Fl., 13.0 Ml; - 25-Fold Concentrate Of Phosphate-Buffered Saline Solution With Tween (Fsb-T×25) – 1 Vial, 28.0 Ml; - Stop Reagent, Ready For Use – 1 Vial, 12.0 Ml. The Set Is Additionally Equipped With: - Films For Sealing The Tablet - 3 Pcs., - Baths For The Reagent - 2 Pcs., - Tips For Pipettes For 5-200 Μl - 16 Pcs., Set Of Reagents For Enzyme Immunoassay Detection Of Hbsag. Composition: - Collapsible Tablet With Immobilized Monoclonal Antibodies To Hbsag – At Least 5 Pcs.; - Positive Control Sample (K+), Inactivated, Contains (4.0±2.0) Iu/Ml Hbsag - At Least 2 Fl. 1.5 Ml Each; - Weakly Positive Control Sample (K+Weak), Inactivated, Contains (0.2±0.1) Iu/Ml Hbsag - At Least 2 Fl. 1.5 Ml Each; - Negative Control Sample (K–), Inactivated – At Least 2 Fl. 2.5 Ml; - Conjugate, Concentrate - Polyclonal Antibodies To Hbsag, Labeled With Horseradish Peroxidase - At Least 3 Fl. 1.4 Ml Each; Solution For Diluting The Conjugate (Rc) – At Least 3 Fl. 14 Ml Each; - Phosphate-Buffered Saline Solution Concentrate With Tween (Fsb-T×25) - No Less Than 1 Fl., 100 Ml; - Tetramethylbenzidine, Concentrate (Tmb) - No Less Than 3 Fl. 1.5 Ml Each; - Substrate Buffer Solution (Sbs) - At Least 3 Fl. 20 Ml Each; - Stop Reagent – ​​At Least 3 Fl. 21 Ml Each. The Kit Is Additionally Equipped With: - Films For Sealing The Plate - At Least 10 Pcs.; - Baths For Reagents - At Least 10 Pcs.; - Tips For Pipettes For 4-200 Μl - At Least 80 Pcs. The Kit Is Designed To Carry Out At Least 480 Determinations, Including Controls. Fractional Use Of The Kit Is Allowed (From One Strip) With The Ability To Conduct Up To 16 Independent Analytical Series. The Kit Can Be Used In Automatic Open-Type Elisa Analyzers. The Shelf Life Of The Reagent Kit Is At Least 24 Months From The Date Of Release. Mandatory Condition For Delivery: - Availability Of A Registration Certificate. - Certificate Of Product Conformity, - Availability Of Approved Instructions For Use. Labeling Of A Medical Device, Standard Erythrocyte Panels For Determining Blood Groups Using The Reverse Method On The Saho Biorad Apparatus. 1 Package - At Least 2 Bottles * 10 Ml, 1 Package For At Least 100 Studies