Hangzhou Funworld Biotech Co.,Ltd

Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

favorite supplier

verified Gold Member
Hangzhou Funworld Biotech Co.,Ltd
favorite supplier

Hangzhou Funworld Biotech Co.,Ltd

Zhejiang,China

Scan QR code

Access to mobile station

Clear All
Alternate Text

COVID-19 Ag Rapid Test Device (Nasopharyngeal swabs/ Nasal swab/Saliva)

FOB Price : Get a Price/Quote

Min.Order : 1000 Piece(s)

Certification : ISO13485,CE

Brand Name : Funworld

Payment Terms : T/T,D/P

share :

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 : China

product description

The detection of SARS-COV-2 adopts the principle of double antibody sandwich method and colloidal gold immunochromatography to qualitatively detect SARS-COV-2 antigen in human Nasopharyngeal swabs, Nasal swab, Saliva, etc., with two highly specific and highly sensitive SARS-COV- 2 N antigen monoclonal antibodies, wherein monoclonal antibody I is a capture antibody, fixed in the detection area on the NC membrane, monoclonal antibody II is a colloidal gold-labeled antibody, sprayed on the binding pad, and the NC membrane quality control area C is coated with goat anti-chicken IgY antibody. The double antibody sandwich method is used in the detection area, and the antigen-antibody reaction is used in the quality control area, combined with colloidal gold immunochromatography technology to detect the SARS-COV-2 in the human body. During detection, the sample is chromatographed under the capillary effect. If the tested sample contains SARS-COV-2, the gold-labeled SARS-COV-2 N antigen monoclonal antibody I combines with SARS-COV-2 to form a complex, and combines with the a SARS-COV-2 N antigen monoclonal antibody II fixed at the detection line during the chromatography process, which will form the "Au-antibody I-N antigen- antibody II" sandwich, so that a purple band appears in the detection area (T); Otherwise, no magenta bands appear in the detection area (T). Regardless of whether there is a SARS-COV-2 antigen in the sample, the complex will continue to be chromatographed up to the control area (C), and a purple band appears when reacting with the goat anti- chicken IgY. The purple-red band presented in the control area (C) is a standard for judging whether the chromatographic process is normal, and also serves as an internal control standard for reagents.

People who viewed this also viewed

  • Prostate Specific Antigen Rapid Test Device (Whole Blood/Serum/Plasma)

    FOB Price :

    Min.Order : 1000 Piece(s)

  • Malaria Pf Rapid Test Strip (Whole Blood)

    FOB Price :

    Min.Order : 1000 Piece(s)

  • H. Pylori Ab Rapid Test Strip (Whole Blood/Serum/Plasma)

    FOB Price :

    Min.Order : 1000 Piece(s)

  • fFN rapid test Strip (Vaginal secretion)

    FOB Price :

    Min.Order : 1000 Piece(s)

  • HIV 1/2 Rapid Test Strip (WB/S/P)

    FOB Price :

    Min.Order : 1000 Piece(s)

COVID-19 Ag Rapid Test Device (Nasopharyngeal swabs/ Nasal swab/Saliva)
share :

product information

product description

The detection of SARS-COV-2 adopts the principle of double antibody sandwich method and colloidal gold immunochromatography to qualitatively detect SARS-COV-2 antigen in human Nasopharyngeal swabs, Nasal swab, Saliva, etc., with two highly specific and highly sensitive SARS-COV- 2 N antigen monoclonal antibodies, wherein monoclonal antibody I is a capture antibody, fixed in the detection area on the NC membrane, monoclonal antibody II is a colloidal gold-labeled antibody, sprayed on the binding pad, and the NC membrane quality control area C is coated with goat anti-chicken IgY antibody. The double antibody sandwich method is used in the detection area, and the antigen-antibody reaction is used in the quality control area, combined with colloidal gold immunochromatography technology to detect the SARS-COV-2 in the human body. During detection, the sample is chromatographed under the capillary effect. If the tested sample contains SARS-COV-2, the gold-labeled SARS-COV-2 N antigen monoclonal antibody I combines with SARS-COV-2 to form a complex, and combines with the a SARS-COV-2 N antigen monoclonal antibody II fixed at the detection line during the chromatography process, which will form the "Au-antibody I-N antigen- antibody II" sandwich, so that a purple band appears in the detection area (T); Otherwise, no magenta bands appear in the detection area (T). Regardless of whether there is a SARS-COV-2 antigen in the sample, the complex will continue to be chromatographed up to the control area (C), and a purple band appears when reacting with the goat anti- chicken IgY. The purple-red band presented in the control area (C) is a standard for judging whether the chromatographic process is normal, and also serves as an internal control standard for reagents.

Recommend

Join Free

Create New Account

Leave your contact information for the suppliers. If you're our member, Please Sign In to use your account information.

Sign in