SARS-CoV-2 Spike Trimer (JN.1) ELISA Kit (For Vaccine Development)

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RAS-A199-96tests
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Materials Provided

ID
Components
Size
RAS199-C01
Pre-coated Anti-SARS-CoV-2 Spike Trimer (JN.1) Antibody Microplate
1 plate
RAS199-C02
SARS-CoV-2 Spike Trimer (JN.1)
30 μg
RAS199-C03
Biotin-Anti-SARS-CoV-2 Spike Trimer Antibody
100 μL
RAS199-C04
Streptavidin-HRP
10 μg
RAS199-C05
10xWashing Buffer
50 mL
RAS199-C06
2xDilution Buffer
50 mL
RAS199-C07
Substrate Solution
12 mL
RAS199-C08
Stop Solution
7 mL

Product Overview

The newly identified Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has posed a serious threat to human health. A rapid and effective assay kit detecting the levels of SARS-CoV-2 Spike protein is urgently needed to accelerate the development of COVID-19 vaccines.

Application

This kit is developed for quantitative detection of SARS-CoV-2 Spike Trimer (JN.1) in samples.

It is for research use only.

Reconstitution

Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.

Storage

1. Unopened kit should be stored at 2℃-8℃ upon receiving.

2. Find the expiration date on the outside packaging and do not use reagents past their expiration date.

3. The opened kit should be stored per components table. The shelf life is 30 days from the date of opening.

Assay Principles

This assay kit employs a standard sandwich-ELISA format, providing a rapid detection of SARS-CoV-2 Spike Trimer (JN.1). The kit consists of microplate pre-coated with Anti-SARS-CoV-2 Spike Trimer (JN.1) Antibody, an SARS-CoV-2 Spike Trimer (JN.1) as Control,biotin-Anti-SARS-CoV-2 Spike Trimer Antibody, HRP-Streptavidin and buffers.

Your experiment will include 6 simple steps:

a) Bring all reagents and samples to room temperature (20℃-25℃) before use.

b) Add your sample to the plate, take the SARS-CoV-2 Spike Trimer as Control sample. The samples and Control sample are diluted by Dilution Buffer.

c) Add the Secondary antibody biotin-Anti-SARS-CoV-2 Spike Trimer Antibody diluted by Dilution Buffer to the plate.

d) Add the diluted Streptavidin-HRP to the plate.

e) Wash the plate and add TMB or other colorimetric HRP substrate.

f) Stop the substrate reaction by adding diluted acid. Absorbance (OD) is calculated as the absorbance at 450 nm minus the absorbance at 630 nm to remove background prior to statistical analysis. The OD Value reflects the amount of protein bound.