膜杰作
Star Staining
| ID | Components | Size |
| RAS070-C01 | Pre-coated SARS-CoV-2 Spike Trimer(B.1.617.2) Microplate | 1 plate |
| RAS070-C02 | Positive Control | 100 μL |
| RAS070-C03 | Negative Control | 100 μL |
| RAS070-C04 | HRP-Conjugated Antibody | 10 μg |
| RAS070-C05 | 10xWashing Buffer | 50 mL |
| RAS070-C06 | Dilution Buffer | 50 mL |
| RAS070-C07 | Substrate Solution | 12 mL |
| RAS070-C08 | Stop Solution | 7 mL |
背景（Background）
Identification of some familiar mutations that also appeared on other VOCs gives rises to concerns of its immune escape potential and higher transmissibility. To facilitate the mutant-related research, drug trials and vaccine development, a high-throughput assay to measure IgG antibodies against the mutants is in urgent need.
应用说明（Application）
This kit is developed for titer measurement of Anti-SARS-CoV-2 (B.1.617.2) Antibody IgG in Mouse serum.
It is for research use only.
重构方法（Reconstitution）
Please see Certificate of Analysis for details of reconstitution instruction and specific concentration.
存储 & 运输（Storage & Shipping）
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.
原理（Assay Principles）
This assay kit employs a standard indirect-ELISA format, providing a rapid detection of Anti-SARS-CoV-2 antibodies in Mouse serum by SARS-CoV-2 Spike Trimer. The Kit consists of Pre-coated with SARS-CoV-2 Spike Trimer Microplate, an Positive Control, an Negative Control, an HRP-Anti-Goat anti mouse IgG secondary antibody.
Your experiment will include 4 simple steps:
a) The samples and Control are diluted by Dilution Buffer. Add your sample to the plate.
b) Add diluted Secondary antibody HRP-Goat anti-Mouse IgG to the plate.The Secondary antibody is diluted by Dilution Buffer.
c) Wash the plate and add TMB or other colorimetric HRP substrate.
d) Stop the substrate reaction by add 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 antibody bound.
