Hangzhou Funworld Biotech Co.,Ltd

Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

Hangzhou Funworld Biotech Co.,Ltd
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Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

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HIV 1/2 Rapid Test Device(WB/S/P)

FOB Price : Get a Price/Quote

Min.Order : 1000 Piece(s)

Certification : ISO13485,CE

Brand Name : Funworld

Payment Terms : T/T,D/P

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product information

  • brand name : Funworld

  • certification : ISO13485,CE

  • min.order : 1000 Piece(s)

  • warranty : 2 years

  • payment terms : T/T,D/P

  • Packaging : Standard Export Carton

  • Specification : 25 Tests/ box

  • place of origin : Zhejiang

product description

The HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative, membrane based immunoassay for the detection of antibodies to HIV 1/2 in whole blood, serum or plasma. The membrane is pre‐coated with recombinant HIV antigens. During testing, the whole blood, serum or plasma specimen reacts with HIV antigen coated particles in the test strip. The mixture then migrates upward on the membrane chromatographically by capillary action and reacts with recombinant HIV antigen on the membrane in the test line region. If the specimen contains antibodies to HIV 1 and/or HIV 2, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain HIV 1 and/or HIV 2 antibodies, a colored line will not appear in the test line region indicating a negative result. To serve as a procedural control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.

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HIV 1/2 Rapid Test Device(WB/S/P)
share :

product information

product description

The HIV 1/2 Human Immunodeficiency Virus Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative, membrane based immunoassay for the detection of antibodies to HIV 1/2 in whole blood, serum or plasma. The membrane is pre‐coated with recombinant HIV antigens. During testing, the whole blood, serum or plasma specimen reacts with HIV antigen coated particles in the test strip. The mixture then migrates upward on the membrane chromatographically by capillary action and reacts with recombinant HIV antigen on the membrane in the test line region. If the specimen contains antibodies to HIV 1 and/or HIV 2, a colored line will appear in the test line region indicating a positive result. If the specimen does not contain HIV 1 and/or HIV 2 antibodies, a colored line will not appear in the test line region indicating a negative result. To serve as a procedural control, a colored line will always appear in the control line region indicating that proper volume of specimen has been added and membrane wicking has occurred.

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