The SARS-CoV-2 IgG ELISA kit is a colorimetric immunoassay kit with results in under 2 hours. Absorbance is read at 450 nm. Measure up to 86 samples with 1 kit.

Schematic diagram of the assay protocol for the SARS-CoV-2 IgG ELISA Kit.

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Product Details

Alternative Name:	Coronavirus (COVID-19) IgG

Assay Time:	<2 hours

Applications:	ELISA, Colorimetric detection

Application Notes:	For the qualitative determination of human SARS-CoV-2 IgG in serum.

Wavelength:	450 nm

Species reactivity:	Human

Shipping:	Blue Ice Not Frozen

Long Term Storage:	+4°C

Contents:	SARS-CoV-2 Antigen Coated Microplate High Positive Control Low Positive Control Negative Control Sample Diluent Wash Buffer Concentrate Stop Solution TMB Substrate HRP Conjugate Plate Sealer

Technical Info/Product Notes:	SARS-CoV-2 IgG ELISA Kit - Fact Sheet for Healthcare Providers SARS-CoV-2 IgG ELISA Kit - Fact Sheet for Recipients

Regulatory Status:	IVD - For In vitro Diagnostic Use Only, Rx Only - For Prescription Use Only

Disclaimer:	The SARS-CoV-2 IgG ELISA Kit is an Enzyme-Linked Immunosorbent Assay (ELISA) intended for qualitative detection of IgG antibodies to SARS-CoV-2 in human serum. The SARS-CoV-2 IgG ELISA Kit is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity. Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C 263a, to perform moderate or high complexity tests. Results are for the detection of SARS CoV-2 antibodies. IgG antibodies to SARS-CoV-2 are generally detectable in blood several days after initial infection, although the duration of time antibodies are present post-infection is not well characterized. Individuals may have detectable virus present for several weeks following seroconversion. Laboratories within the United States and its territories are required to report all positive results to the appropriate public health authorities. This test has been validated but FDA’s independent review of this validation is pending. Negative results do not preclude acute SARS-CoV-2 infection. If acute infection is suspected, direct testing for SARS-CoV-2 is necessary. Results from antibody testing should not be used to diagnose or exclude acute SARS-CoV-2 infection. Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E. This test should not be used for screening of donated blood.

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