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SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection

Shenzhen Kisshealth Biotechnology Co., Ltd
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SARS-CoV-2 Antigen Detection Kit Rtk Saliva Accuracy Delta Variant Detection

Brand Name : KISSH

Model Number : K903-1

Certification : CE

Place of Origin : CHINA

MOQ : 1000 tests

Price : Negotiable

Payment Terms : T/T

Supply Ability : 1,000,000 tests per day

Delivery Time : Within 7 days

Packaging Details : 1 Test/Kit, 5 Tests/Kit, 10 Tests/Kit, 20 Tests/Kit

Product namee : SARS-CoV-2 Antigen Detection Kit(Immunofluorescence)

Usage : Qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP), nasal swab and saliva specimens

Sample Type : Nasopharyngeal (NP) and Nasal swab,Saliva,Oropharyngeal (OP) swab

Pattern : KISSH

Methodology : Immunofluorescence

Function : Delta Variant Detection

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SARS-CoV-2 Antigen Detection Kit(Immunofluorescence)

Product Information

Product name SARS-CoV-2 Antigen Detection Kit(Immunofluorescence)
Main Composition Test Cassette individually foil pouched with a desiccant, Sample Tube, with cap and antigen extraction buffer,Sampling swab, Instruction for use
Package 1 Test/Kit
Keep temperature 2-30℃
Shelf-life 12 months
Place of Origin Shenzhen China

Basis Information

The SARS-CoV-2 Antigen Detection Kit is a fluorescence immunoassay that is intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal (NP) and nasal swab, saliva specimens and superficial nasal swab directly from individuals who are suspected of COVID- 19 by their healthcare provider.

Results are for the identification of SARS-CoV-2 nucleocapsid protein antigen. Antigen is generally detectable in upper respiratory specimens during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out bacterial infection or co-infection with other viruses. The agent detected may not be the definite cause of disease.

Negative results should be treated as presumptive and confirmed with a molecular assay, if necessary for patient management. Negative results do not rule out COVID- 19 and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID- 19.The SARS-CoV-2 Antigen Test is intended for use by trained clinical laboratory personnel and individuals trained in point of care settings.


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SARS-CoV-2 Antigen Detection Kit

      

Rtk Saliva Accuracy Delta Variant Detection

      

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