SARS-CoV-2 Spike RBD Titer Assay Kit | RAS-A021

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SKU:
RAS-A021
Sample:
Human Serum
Size:
96 Tests
zł3,096.08
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Description

SARS-CoV-2 Spike RBD Titer Assay Kit | RAS-A021 | Acro Biosystems | SARS-CoV-2 Antigen Titer Assay Kits

Background
 
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 RBD is urgently needed to accelerate the development of COVID-19 vaccines.
 
Application
 
This kit is developed for detecting SARS-CoV-2 Spike RBD in the sample.
It is for research use only.
 
Reconstitution
 
Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.
 
Storage
 

The unopened kit is stable for at least 1 year from the date of manufacture if stored at 2°C to 8°C, and the opened kit is stable for up to 1 month from the date of opening at 2°C to 8°C.

It is recommended not to freeze thaw more than 3 times for powder.

This product is stable under storage conditions: ● 12 months in sealed state. ● Used within 1 months after opening.

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

Your experiment will include 6 simple steps:

a)  All reagents were returned to room temperature(20℃-25℃) before use.

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

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

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

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

f)  Stop the substrate reaction by add diluted acid. Absorbance (OD) is calculated as the absorbance at 450 nm minus the absorbance at 650 nm to remove background prior to statistical analysis. The OD Value reflects the amount of protein bound.

Typical Data
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