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2021 High quality Fluorescence Immunoassay Instrument - KaiBiLi COVID-19 IgG/IgM – Genesis


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Our growth depends on the superior equipment ,exceptional talents and continuously strengthened technology forces for Antigen Rapid Test Results, SARS-CoV-2, Saliva Sampling, Standing still today and searching into the long run, we sincerely welcome shoppers all around the globe to cooperate with us.
2021 High quality Fluorescence Immunoassay Instrument - KaiBiLi COVID-19 IgG/IgM – Genesis Detail:

Introduction

The KaiBiLiTM COVID-19 IgG/IgM Rapid Test Device is a lateral flow chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to 2019- Novel Coronavirus in human whole blood, serum or plasma specimen. It is only used as a supplementary detection indicator for new suspected cases of negative coronavirus nucleic acid detection or in conjunction with nucleic acid detection in the diagnosis of suspected cases. It cannot be used as a basis for the diagnosis and exclusion of pneumonitis infected by 2019-nCoV infection. It is not suitable for general population screening.

Any reactive specimen with the COVID-19 IgG/IgM Rapid Test Device must be confirmed with alternative testing method(s) and clinical findings. A positive test result requires further confirmation. A negative results do not preclude acute 2019-nCoV infection. If acute infection is suspected, direct testing for COVID-19 antigen is necessary. False positive results for COVID-19 IgG/IgM Rapid Test may occur due to cross-reactivity from preexisting antibodies or other possible causes. Due to the risk of false positive results, confirmation of positive results should be considered using second, different IgG or IgM assay.

Detection

The COVID-19 IgG/IgM Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative lateral flow immunechromatographic assay for the detection of IgG and IgM antibodies to 2019-nCoV in whole blood, serum or plasma specimen. 

Specimen

IgG and IgM antibodies to 2019 nCoV in whole blood, serum or plasma specimen.

Accuracy

IgG Result:

Relative Sensitivity: 98.28%   

Relative Specificity: 97.01%  

Accuracy: 97.40%

IgM Result:

Relative Sensitivity: 82.76%  

Relative Specificity: 98.51% 

Accuracy: 93.75%  

Time to Results

Read results at 15minutes and no more than 30 minutes. 

Kit storage conditions

2~30°C. 

Contents

  P231133 P231134 P231135
COVID-19 IgG/IgM test device 40 pcs 30 pcs 1 each 
Sample buffer 5mL/Bot.

1Bot

80μl/vial 

30 vial

 80μl/vial 

1 vial

Capillary dropper* 40 pcs 30 pcs  1 each
Package insert 1 each 1 each 1 each

*Capillary dropper: For whole blood.

Ordering Information

Product

Cat.No.

Contents

KaiBiLiTM COVID-19 IgG/IgM P231133 40 Tests
KaiBiLiTM COVID-19 IgG/IgM P231134 30 Tests
KaiBiLiTM COVID-19 IgG/IgM P231135 1 Tests

Product detail pictures:

2021 High quality Fluorescence Immunoassay Instrument - KaiBiLi COVID-19 IgG/IgM – Genesis detail pictures

2021 High quality Fluorescence Immunoassay Instrument - KaiBiLi COVID-19 IgG/IgM – Genesis detail pictures

2021 High quality Fluorescence Immunoassay Instrument - KaiBiLi COVID-19 IgG/IgM – Genesis detail pictures


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As for competitive charges, we believe that you will be searching far and wide for anything that can beat us. We will state with absolute certainty that for such excellent at such charges we have been the lowest around for 2021 High quality Fluorescence Immunoassay Instrument - KaiBiLi COVID-19 IgG/IgM – Genesis , The product will supply to all over the world, such as: Switzerland, Malaysia, Jersey, Due to good quality and reasonable prices, our items have been exported to more than 10 countries and regions. We are looking forward to cooperating with all customers from at home and abroad. Moreover, customer satisfaction is our eternal pursuit.
This is a honest and trustworthy company, technology and equipment are very advanced and the prodduct is very adequate, there is no worry in the suppliment.
5 Stars By Janet from Jamaica - 2018.12.28 15:18
This company can be well to meet our needs on product quantity and delivery time, so we always choose them when we have procurement requirements.
5 Stars By Michaelia from Chicago - 2017.12.31 14:53
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