Recombinant SARS-CoV-2 Spike S2 Subunit His-tag Protein, CF Summary
Details of Functionality |
Bioassay data are not available. |
Source |
Trichoplusia ni, T. ni (baculovirus)-derived sars-cov-2 Spike S2 Subunit protein Ser686-Lys1211, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Ser686 |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
Dilutions |
|
Theoretical MW |
60 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
SDS-PAGE |
65-75 kDa, under reducing conditions |
Packaging, Storage & Formulations
Storage |
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 3 months, -20 to -70 °C under sterile conditions after reconstitution.
|
Buffer |
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. |
Purity |
>95%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining. |
Reconstitution Instructions |
Reconstitute at 500 μg/mL in PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant SARS-CoV-2 Spike S2 Subunit His-tag Protein, CF
Background
SARS-CoV-2,
which causes the global pandemic coronavirus disease 2019 (Covid-19), belongs
to a family of viruses known as coronaviruses that also include MERS and
SARS-CoV-1. Coronaviruses are commonly comprised of four structural proteins:
Spike protein(S), Envelope protein (E), Membrane protein (M) and Nucleocapsid
protein (N) (1). SARS-CoV-2 Spike Protein (S Protein) is a glycoprotein that
mediates membrane fusion and viral entry. The S protein is homotrimeric, with
each ~180-kDa monomer consisting of two subunits, S1 and S2 (2). As with most coronaviruses,
proteolytic cleavage of the S protein into two distinct peptides, S1 and S2
subunits, is required for activation. The S1 subunit is focused on attachment of
the protein to the host receptor while the S2 subunit is involved with cell
fusion (2-4). A metallopeptidase, angiotensin-converting enzyme 2 (ACE-2), has
been identified as a functional receptor for SARS-CoV2, similar to SARS-CoV-1, through
interaction with a receptor binding domain (RBD) located at the C-terminus of
S1 subunit (5, 6). The S2 subunit of SARS-CoV-2 shares 90% and 41% amino acid
sequence identity with the S2 subunit of SARS-CoV-1 and MERS, respectively. It
has been demonstrated the S Protein can invade host cells through the
CD147/EMMPRIN receptor and mediate membrane fusion (7, 8).
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