GTR 113418438
Request For Quotation Laboratory Consumables/Zerthanalyk Shygyn Materials
ICB — International Competitive Bid
Closed
Central Asia
Tender Information
GTR Reference
113418438
Tendering Authority
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Tender No
17044888
Financer Name
Self-Funded
Work Title
Request For Quotation Laboratory Consumables/Zerthanalyk Shygyn Materials
Bid Type
ICB — International Competitive Bid
Country
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Geographical Region
Central Asia
Political Region
Commonwealth of Independent States, CIS
Last Date of Bid Submission
25-05-2026
Closed
Work Detail
Immunochromatographic Express Test For Determining Antibodies To The Hepatitis C Virus Hexagon Hcv Immunochromatographic Express Test For Determining Antibodies To The Hepatitis C Virus Hexagon Hcv. 40 Tests Kit Contains: 1. 40 Pcs Single-Use Test Devices With Recombinant (E. Coli) Hcv Antigens (Core, Ns3, Ns4 And Ns5), Dye-Protein A Conjugate And Goat Anti-Human Ig Antibodies, Individually Packaged In Sealed Bags. 2. 7 Ml Solution For Diluting Samples: Tris Buffer (50 Mmol/L) With The Addition Of Sodium Azide (0.02% W/V). 3. 40 Pcs Single Use Pipettes With A Volume Of About 10 Μl When Drawing To The Black Mark. Each Kit Contains Reagents Sufficient For 40 In Vitro Diagnostic Studies. Hexagon Hcv Is Based On An Immunochromatographic Method Using Recombinant Antigens Representing The Core, Ns3, Ns4 And Ns5 Regions Of The Hcv Genome, Which Are Known To Be Highly Immunodominant. These Antigens Are Fixed In A Test Line (T) On The Membrane. Protein A, As An Igg Reactive Material, Is Bound To The Dye And Located In The Conjugate Pad On The Strip. A Small Area Of The Membrane Is Prepared Using Anti-Human (Goat) Ig Antibodies To Form A Control Line (C). As The Sample Passes Through The Absorbent Pad, Anti-Hcv Antibodies Specific For The Recombinant Antigens Bind To The Protein A-Dye Conjugate To Form Immune Complexes. They Bind To The Corresponding Recombinant Antigens In The Test Line (T) And Form A Red-Violet Line. Excess Conjugate Is Reacted In The Control Line (C) To Demonstrate Proper Functioning Of The Reagents And Proper Test Performance. When Stored At 2...30°C, The Test Is Stable Until The Indicated Expiration Date. Whole Blood, Plasma Or Serum Samples Can Be Used. Sensitivity: 99.3%. Specificity: 99.5%, Hiv Ag/Ab 4Th Gen. Rapid Test, (Cassettes) Express Test Hiv Antigen/Ab 4Th Generation Rapid Test Is A Lateral Flow Immunoassay For The Qualitative Detection Of Antibodies To The Hiv-1 Virus (Including O) And The Hiv-2 Virus (Igg, Igm, Iga), As Well As The Hiv-1 P24 Antigen In Human Serum, Plasma Or Whole Blood. It Is Intended For Use By Healthcare Professionals To Diagnose Hiv Infection. The Presence Of Specific Antibodies To The Hiv-1 Or Hiv-2 Virus In Whole Blood, Serum Or Plasma Indicates A Persons Exposure To Hiv-1 Or Hiv-2, Which Is Of Great Importance For Clinical Diagnosis. The Hiv P24 Antigen Test Is Useful For The Early Diagnosis Of Hiv, Since The P24 Antigen Is One Of The Earliest Markers Of Hiv Infection. The Test Strip In The Cassette Consists Of: 1) A Colored Pad With A Conjugate Containing Recombinant Hiv Gp120-41 And Gp-36 Antigens Conjugated With Colloidal Gold (Hiv Conjugates), A Monoclonal Antibody Anti-Hiv-P24 Conjugated To Colloidal Gold (P24 Conjugates) And A Control Antibody Conjugated To Colloidal Gold, 2) A Nitrocellulose Membrane Strip Containing Two Test Lines (Ag Line And Ab Line) And A Control Line (C Line). The Ab Line Is Precoated With Hiv-Gp120-41 And Hiv-2 Gp-36 Antigens To Detect Antibodies To Hiv-1, Including O Or Hiv-2, The Ag Line Is Precoated With Another Monoclonal Anti-Hiv P24 Antibody To Detect The P24 Antigen, And The C Line Is Precoated With A Control Line Antibody. Relative Sensitivity: 100% (95% Ci: 97.5–100%) Relative Specificity: 100% (95% Ci: 98.9–100%) Ingredients: Individually Packaged Cassettes And Sample Diluent, Instructions. Designed For Reading On The Alta Analyzer. Installation And Activation Of The Test Kit On Board The Analyzer Through The Manufacturers Server Is Required., Immunochromatographic One-Step Test For The Determination Of Hepatitis B Surface Antigen (Hbsag) In Serum Or Blood Plasma “Hexagon Hbsag” 3 X 20 Tests Hepatitis B Hexagon Is A One-Step Immunochromatographic Test Designed For The Qualitative Determination Of Hepatitis B Surface Antigen (Hbsag) In Human Serum Or Plasma. During The Analysis, A Sample Of Blood Serum Migrates Along The Membrane. If Hbsag Is Present In The Serum, It Reacts With Mouse Monoclonal Antibodies To Hbsag Adsorbed On Colloidal Gold Particles. The Immune Complexes Formed As A Result Of The Reaction Migrate Along With The Liquid To The Results Zone, Where They Bind To Immobilized Secondary Mouse Monoclonal Antibodies To Hbsag. As A Result, A Red Stripe Appears On The Test Strip. Unbound Immune Complexes And/Or Colloidal Particles Migrate Further, Reacting With Immobilized Rabbit Anti-Mouse Igg Antibodies To Form A Control Colored Band. The Appearance Of The Latter Indicates The Correct Execution Of The Test. Thus, If Hbsag (>1 U/Ml) Is Present In The Sample, Two Colored Lines Will Form On The Test Strip. If Hbsag Is Absent Or Its Concentration Is Less Than 1 U/Ml, Only One Control Line Appears. The Absence Of Visible Lines In The Results Area Indicates That The Test Was Performed Incorrectly Or The Test Strip Is Unusable. Kit Contents: 3 X 20 Test Strips In Plastic Containers. Stopper With Desiccant, 2 Additional Bags Of Silica Gel. The Test Strips Are Coated With Monoclonal Anti-Hbs (Mouse), Hemocyanin (Shellfish), Immobilized Monoclonal Anti-Hbs (Mouse), And Anti-Hemocyanin (Mouse). Hexagon Hbsag Is Stable Until The Stated Expiration Date When Stored At 2...25°C In A Dry Place. Samples: Serum Or Plasma (Edta, Citrate, Heparin)., Slide Glass With Polished Edges 75X50xl Mm
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3,620,000 - KZT
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