Recombinant SARS-CoV-2, Nucleocapsid (N) Protein

Cat# S854-500

Size : 500µg

Brand : Leinco Technologies

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Recombinant SARSCoV2, Nucleocapsid (N) Protein

Product No.: S854

Alternate Names
Nucleocapsid Protein, N Protein SARSCoV2
Product Type
Recombinant Protein
Expression Host
HEK293 Cells
Species
SARSCoV2
Virus
Applications
ELISA
WB

Data

N Protein (Prod. No. S854) DataPurified SARSCoV2 Nucleocapsid (N) Protein (Prod. No. S854)

Background

Severe acute respiratory syndrome coronavirus 2 (SARSCoV2), the causative agent of coronavirus disease 2019 (COVID19), is an enveloped, singlestranded, positivesense RNA virus that belongs to the Coronaviridae family1. The SARSCoV2 genome, which shares 79.6% identity with SARSCoV, encodes four essential structural proteins: the spike (S), envelope (E), membrane (M), and nucleocapsid protein (N)2. The N protein is 46 kDa and consists of two highly conserved structural domains, the Nterminal domain (NTD) and Cterminal domain (CTD), connected by a linker region. The NTD and CTD are involved in RNA binding and selfoligomerization, respectively3,4. The primary function of the N protein is to bind to and package the viral RNA genome into a helical ribonucleoprotein complex5. The N protein is also involved in other critical steps of the viral life cycle, including transcription, replication, and modulating infected cell signaling pathways6,7. The N protein is abundantly expressed during infection and is highly conserved, sharing 90% amino acid homology with the SARSCoV N protein (8). It is also immunogenic, and antibodies8,9 and memory T cells 10,11 targeting the N protein are present in the sera of convalescent COVID19 patients, identifying the N protein as a suitable candidate for vaccine development and diagnostic assays. Diagnostic assays based on the N protein effectively detect antibodies in the sera of patients infected with SARSCoV212. The N protein also contributes to immune evasion by antagonizing antiviral RNAi13, suggesting its potential value as a targeted therapeutic.

Protein Details

Format
Purified No Carrier Protein
Purity
>95% by SDS Page
Product Concentration
0.5 mg/ml
Endotoxin Level
<0.10 EU per 1 μg of the protein by the LAL method
Protein Accession No.
Amino Acid Sequence
MSDNGPQNQRNAPRITFGGPSDSTGSNQNGERSGARSKQRRPQGLPNNTASWFTALTQHGKEDLKFPRGQGVPINTNSSPDDQIGYYRRATRRIRGGDGKMKDLSPRWYFYYLGTGPEAGLPYGANKDGIIWVATEGALNTPKDHIGTRNPANNAAIVLQLPQGTTLPKGFYAEGSRGGSQASSRSSSRSRNSSRNSTPGSSRGTSPARMAGNGGDAALALLLLDRLNQLESKMSGKGQQQQGQTVTKKSAAEASKKPRQKRTATKAYNVTQAFGRRGPEQTQGNFGDQELIRQGTDYKHWPQIAQFAPSASAFFGMSRIGMEVTPSGTWLTYTGAIKLDDKDPNFKDQVILLNKHIDAYKTFPPTEPKKDKKKKADETQALPQRQKKQQTVTLLPAADLDDFSKQLQQSMSSADSTQA
State of Matter
Liquid
Predicted Molecular Mass
The predicted molecular weight of Recombinant SARSCoV2, Nucleocapsid (N) Protein is Mr 47 kDa.
Predicted Molecular Mass
47 kDa
Formulation
This recombinant protein is aseptically packaged and formulated in 0.01 M phosphate buffered saline (PBS) pH 7.2 7.4, 150 mM NaCl with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of proteins, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration.
Storage and Stability
We recommended to store this recombinant protein as received at 28°C for up to one month. For longerterm storage, aseptically aliquot in working volumes without diluting and store at 80°C. Avoid Repeated Freeze Thaw Cycles.
Country of Origin
USA
Shipping
Blue Ice via Next Day Air
NCBI Gene Bank
Applications and Recommended Usage ?
(Quality Tested by Leinco)
ELISA
WB

References & Citations

1. Zhou, P., Yang, X., Wang, X. et al. Nature 579, 270–273. 2020.
2. Wu, F., Zhao, S., Yu, B. et al. Nature 579, 265–269. 2020.
3. Kang S, Yang M, Hong Z, et al. Acta Pharm Sin B. 2020
4. Chang CK, Sue SC, Yu TH, et al. J Biomed Sci. 13(1):5972. 2006
5. Hsieh PK, Chang SC, Huang CC, et al. J Virol. 79(22):1384813855. 2005
6. Surjit M, Lal SK. Infect Genet Evol. 8(4):397405. 2008
7. Hurst KR, Ye R, Goebel SJ, Jayaraman P, Masters PS. J Virol. 84(19):1027610288. 2010
8. Guo L., Ren L., et al. Diseases Society of America. 2020
9. To K.K., Tsang O.T., et al. Lancet Infect. Dis. 2020
10. Grifoni A, Weiskopf D, Ramirez SI, et al. Cell. 181(7):14891501.e15. 2020
11. Ni L, Ye F, Cheng ML, et al. Immunity.52(6):971977.e3. 2020
12. Liu L, Liu W, Zheng Y, et al. Microbes Infect. 22(45):206211. 2020
13. 26. Mu J, Xu J, Zhang L, et al. Sci China Life Sci. 2020