SARS-CoV-2 (COVID-19) Spike 681P Antibody [8G10B1]
Infectious Disease,COVID-19
- 产品详情
- 实验流程
- 背景知识
Application
| WB, E |
|---|---|
| Other Accession | QHD43416 |
| Host | Mouse |
| Clonality | Monoclonal |
| Isotype | IgG3 |
| Clone Names | S |
| Concentration (mg/ml) | 1 mg/mL |
| Conjugate | Unconjugated |
| Gene ID | 43740568 |
|---|---|
| Alias Symbol | S |
| Other Names | SARS-CoV-2 Spike 681P antibody: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), Surface Glycoprotein, Spike protein |
| Reconstitution & Storage | SARS-CoV-2 Spike 681P antibody can be stored at 4˚C for three months and -20˚C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures. |
| Precautions | SARS-CoV-2 (COVID-19) Spike 681P Antibody [8G10B1] is for research use only and not for use in diagnostic or therapeutic procedures. |
For Research Use Only. Not For Use In Diagnostic Procedures.
Provided below are standard protocols that you may find useful for product applications.
BACKGROUND
In September of 2020 a new lineage of SARS-CoV-2, known as B.1.1.7 and named as Alpha variant, was discovered in the United Kingdom. This lineage developed 14 lineage-specific amino acid replacements and 3 deletions. These changes caused an increase in transmission of Alpha variant (B.1.1.7 lineage) by at least 50%, leading to increased disease severity and higher death rates. The effectiveness of COVID19 vaccines are not affected by the Alpha variant. One of the mutations associated with this lineage is a N501Y in the spike protein of the virus. It is believed that this mutation is able to increase the spike protein's affinity for the host ACE2 receptor and it has been associated with increased infectivity and virulence. B.1.1.7 viruses have also been shown to have a P681H mutation in the cleavage site of spike protein. This location is one of the residues that make up the furin proteolytic cleavage site between S1 and S2 in spike protein.
REFERENCES
Duchene et al. Virus Evolution 6(2): veaa061. Gu et al. Science 369(6511):1603-1607 Hoffmann et al. Molecular Cell 78(4):779-784.e5 Davies et al. Science 372(6538):eabg3055. Davies et al. Nature. 593(7858):270-274. Graham, et al. The Lancet Public Health. 6(5): e335-e345. Horby et al. New & Emerging Threats Advisory Group. 2020;91:264-266.
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