Recombinant SARS-CoV-2 (B.1.617.1) Spike Glycoprotein (S1) RBD, His-tagged
Specification
Related Products
| Cat#: |
HUM-337 |
| Product Name: |
Recombinant SARS-CoV-2 (B.1.617.1) Spike Glycoprotein (S1) RBD, His-tagged |
| Description: |
SARS-CoV-2 (B.1.617.1) RBD mutant from the Kerala variant. Contains amino acid changes E484Q, L452R relative to Wuhan Hu-1. The protein was produced in HEK293 cells and purified from culture supernatant. SARS-CoV-2, previously known as the 2019 Novel Coronavirus (2019-nCoV), causes the pandemic COVID-19 disease. |
| Gene: |
Spike Glycoprotein (S1) RBD |
| Species: |
SARS-CoV-2 (B.1.617.1) |
| Source: |
HEK293 |
| Synonyms: |
SARS-CoV-2 (B.1.617.1) Spike Glycoprotein (S1) RBD |
| Formulation: |
DPBS |
| Notes: |
This product is intended for research and manufacturing uses only. It is not a diagnostic device. The user assumes all responsibility for care, custody and control of the material, including its disposal, in accordance with all regulations. |
| Tags: |
His |
| Background: |
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the virus that causes coronavirus disease 2019 (COVID-19). The sequence WIV04/2019, belonging to the GISAID S clade / PANGOLIN A lineage / Nextstrain 19B clade, is believed to be the original sequence infecting humans (Zhukova et al., 2020). However, there are many thousands of variants of SARS-CoV-2 (Koyama et al., 2020) and subtypes of the virus can be placed into much larger groupings such as lineages or clades.
B.1.617, also known as the "double mutant" variant, was first detected in India in October 2020. Since then, three sub lineages of this variant have been detected, namely B.1.617.1, B.1.617.2 and B.1.617.3. The B.1.617.2 is extremely transmissible and is the fourth strain of the SARS-CoV-2 virus to have undergone a mutation toward a more virulent and transmissible form. The B.1.617 lineage possesses 13 to 17 mutations, three of which are in the virus' spike protein. The E484Q mutation appears to confer the virus increased binding capacity to the human ACE2 receptor and better ability to evade the immune system compared to other variants. The L452R mutation provides a similar enhancement of functions as the E484Q. The third mutation, P681R, may increase the infectivity of the virus particles by facilitating the splicing of a unique precursor protein into its active infective conformation. B.1.617.1 shows potential reduction in neutralization by some monoclonal antibody treatments and reduction in neutralization by post-vaccination sera (WHO; CDC). |
For research use only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.
