SARS-CoV-2 Nucleocapsid Protein IgG ELISA Kit
Item No:
E-EL-E600
Chinese Name:
Alias:
COVID 19 IgG,N protein IgG
Keywords:
Classification:
Retail Price
¥ 2400
Market Price
¥ 1
-
Spec
- 48T
- 96T
- 96T*5
Inventory surplus
3
隐藏域元素占位
- Product Comparison
Describe
Product Properties
| Product specification | 96T,96T*5 |
| Experiment Length | 1.5h |
| Sample type | Human serum, plasma |
| Sample volume | 100 μL |
| Storage conditions | 2-8℃ |
| Test range | Qualitative Assay |
| Product use | This kit is used for the in vitro qualitative detection of SARS-CoV-2 IgG in human serum and plasma. |
| Repeatability | Both intra-batch CV & inter-batch CV are less than 10%. |
| Product alias | COVID 19 IgG,N protein IgG |
| Experiment type | Indirect-ELISA |
Detection principle
The kit uses an indirect ELISA method. The recombinant purified SARS-CoV-2 Nucleocapsid protein (N protein) is pre-coated on the enzyme plate. The anti-SARS-CoV-2 Nucleocapsid protein IgG antibody in the sample or positive control will bind to the precoated SARS-CoV-2 Nucleocapsid protein antigen on the ELISA plate, and the free components will be washed away. Horseradish peroxidase-labeled mouse anti-human IgG secondary antibody is then added to form a SARS-CoV-2 nuclear coat protein antigen-anti-SARS-CoV-2 nuclear coat protein IgG-mouse anti-human IgG secondary antibody immune complex, and the free components are washed away. The chromogenic substrate (TMB) was added, and TMB appeared blue catalyzed by horseradish peroxidase and turned yellow after the addition of termination solution. The OD value was measured at 450 nm using an enzyme marker and compared with the calculated Cut Off value to qualitatively determine whether anti-SARS-CoV-2 nucleocapsid protein IgG antibody was present in the test sample.
Operation steps
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1. Add 100 μL of the sample and the quality control to the corresponding plate wells and incubate at 37°C for 45 minutes. |
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2. Discard the liquid in the plate and wash the plate 3 times. |
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3. Add 100uL of binding solution to each well and incubate at 37°C for 30 minutes. Discard the liquid in the plate and wash the plate 5 times. |
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4. Add 90 μL of the conjugate solution to each well and incubate at 37C for about 15 minutes. |
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5. . Add 50μL of stop solution to each well |
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6. Read immediately at 450nm and process the data |
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