Recombinant HCoV-229E Nucleocapsid His-tag Protein, CF Summary
Details of Functionality |
Bioassay data are not available. |
Source |
Spodoptera frugiperda, Sf 21 (baculovirus)-derived hcov-229e Nucleocapsid protein Met1-Asn389, with a C-terminal 6-His tag |
Accession # |
|
N-terminal Sequence |
Ala2, determined by protein ID. |
Protein/Peptide Type |
Recombinant Proteins |
Purity |
>90%, 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 |
44 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 |
48-53 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 |
>90%, 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 HCoV-229E Nucleocapsid His-tag Protein, CF
Background
HCoV-229E belongs to a family of viruses known as coronaviruses that are
commonly comprised of a large plus-strand RNA genome and four structural
proteins: Spike protein (S), Envelope protein (E), Membrane protein (M), and
Nucleocapsid protein (N). HCoV-229E is a
member of the alpha-coronavirus family and was discovered in 1966 (1, 2). Other well-known human coronaviruses include three
viruses that cause relatively mild respiratory disease: HCoV-NL63, HCoV-HKU1
and HCov-OC43, plus three viruses that caused the Severe Acute Respiratory Syndrome
(SARS-CoV), the Middle East Respirator Syndrome (MERS-CoV), and the global
pandemic Covid-19 (SARS-CoV2). While the S, E and M proteins build up the viral envelop, the N protein is involved transcription, replication, and packaging of the viral RNA genome into a helical ribonucleocapsid (RNP) (3). The CoV-229E N protein is a ~50 kDa protein composed of two independent structural domains connected by a linker region. Both the N-terminal and the linker regions contain RNA binding domains, while the C-terminal region is responsible for the oligomerization of the N protein (4). The CoV‑229E protein shares 45% amino acid sequence identity with CoV-NL63 N protein. the N protein is an abundant protein during coronavirus infection and displays high immunogenic activity. Cross activity of antibodies among different strains should be rigorously tested when designing serological diagnostic kits (5).
- Hamre, D. and J.J. Procknow (1966) Proc. Soc. Exp. Biol. Med. 121:190.
- Van der Hoek, L. et al. (2004) Nat. Med. 10:368.
- Chang, C.K. et al. (2006) J.Biomed. Sci. 13:59.
- Lo, Y. et al. (2013) FEBS Letters. 587:120.
- Chan, K.H. et al. (2005) Clin. Diagn. Lab. Immunol. 12:1317.
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