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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Influenza A+B/ COVID-19 Antigen Rapid Test Device (swab)

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 : 20 Tests/ box

  • place of origin : Zhejiang

product description

The Influenza A+B/SARS-CoV-2 Antigen Rapid Test Device detects influenza A and B viral antigens and SARS-CoV-2 Antigen through visual interpretation of color development on the strip. Anti-influenza A and B antibodies and Anti-SARS-CoV-2 antibodies are immobilized on the test region A, B and N of the membrane respectively. During testing, the extracted specimen reacts with anti-influenza A, B and SARS-CoV-2 antibodies conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient influenza A and B viral antigens or SARS-CoV-2 antigen in the specimen, colored band(s) will form at the according test region of the membrane. The presence of a colored band in the A and/or B and/or N region indicates a positive result for the particular viral antigens, while its absence indicates a negative result.
The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.

 

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Influenza A+B/ COVID-19 Antigen Rapid Test Device (swab)
share :

product information

product description

The Influenza A+B/SARS-CoV-2 Antigen Rapid Test Device detects influenza A and B viral antigens and SARS-CoV-2 Antigen through visual interpretation of color development on the strip. Anti-influenza A and B antibodies and Anti-SARS-CoV-2 antibodies are immobilized on the test region A, B and N of the membrane respectively. During testing, the extracted specimen reacts with anti-influenza A, B and SARS-CoV-2 antibodies conjugated to colored particles and precoated onto the sample pad of the test. The mixture then migrates through the membrane by capillary action and interacts with reagents on the membrane. If there is sufficient influenza A and B viral antigens or SARS-CoV-2 antigen in the specimen, colored band(s) will form at the according test region of the membrane. The presence of a colored band in the A and/or B and/or N region indicates a positive result for the particular viral antigens, while its absence indicates a negative result.
The appearance of a colored band at the control region serves as a procedural control, indicating that the proper volume of specimen has been added and membrane wicking has occurred.

 

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