Anti-SARS-CoV-2 Nucleocapsid (N) (Clone NP1-B9) - Biotin

Cat# LT7081-50

Size : 50µg

Brand : Leinco Technologies

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AntiSARSCoV2 Nucleocapsid (N) (Clone NP1B9) – Biotin

Product No.: LT7081

Product No.LT7081
Clone
NP1B9
Target
SARSCoV2 Nucleocapsid (N)
Product Type
Recombinant Monoclonal Antibody
Alternate Names
COV2NP1B9, SARSCoV2 Nucleocapsid, SARSCoV2 Nucleoprotein, Protein N, SARSCoV N Protein
Isotype
Human IgG1
Applications
ELISA

Antibody Details

Product Details

Reactive Species
SARSCoV2
Virus
Expression Host
HEK293 Cells
Immunogen
SARSCoV2 Nucleocapsid (N) Protein
Product Concentration
0.5 mg/ml
Formulation
This Biotinylated antibody is formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.4, 1% BSA and 0.09% sodium azide as a preservative.
Storage and Handling
This biotinylated antibody is stable when stored at 28°C. Do not freeze.
Country of Origin
USA
Shipping
Ships Overnight on Blue Ice
Applications and Recommended Usage?
Quality Tested by Leinco
ELISA
Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change.

Description

Description

Specificity
AntiSARSCoV2 Nucleocapsid, clone NP1B9, specifically targets an epitope on the SARSCoV2 nucleocapsid protein. Futhermore, it is reported to bind to the oligomerization domain of the N protein.
Background
Severe acute respiratory syndrome coronavirus 2 (SARSCoV2), the causative agent of coronavirus disease 2019 (COVID19), is an enveloped, singlestranded, positivesense RNA virus belonging to the Coronaviridae family1. The SARSCoV2 genome encodes four essential proteins: the spike (S), envelope (E), membrane (M), and nucleocapsid (N) proteins2. SARSCoV2 shares 79.6% identity with the original SARSCoV2. 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 a couple of primary functions, including RNA binding and selfoligomerization3,4. This results in binding to and packaging of the viral RNA genome into a helical ribonucleoprotein5. The N protein is involved in other critical steps of the viral life cycle, including transcription, replication, and modulating infected cell signaling pathways6,7. The N protein is a suitable candidate for vaccine development and diagnostic assays8 for several reasons. It is abundantly expressed during infection and is highly conserved, sharing 90% amino acid homology with the SARSCoV N protein9. Furthermore, antibodies9,10 and memory T cells11,12 targeting the N protein are identified in the sera of convalescent COVID19 patients, demonstrating it as immunogenic. The N protein also suppresses antiviral RNAi, evading the innate immune system13, suggesting its potential value as a targeted therapeutic.
Antigen Distribution
The nucleocapsid protein is expressed in the internal nucleocapsid of SARSCoV2.
NCBI Gene Bank ID
Research Area
COVID19
.
Infectious Disease
.
Seasonal and Respiratory Infections
.
Viral
.
IVD Raw Material

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. 10.1016/j.apsb.2020.04.009. 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. Liu L, Liu W, Zheng Y, et al. Microbes Infect. 22(45):206211. 2020.
9. Guo L., Ren L., Yang S., et al. Clinical Infectious Diseases: an Official Publication of the Infectious Diseases Society of America. 2020.
10. To K.K., Tsang O.T., Leung W.S., et al. Lancet Infect. Dis. 2020.
11. Grifoni A., Weiskopf D., Ramirez S.I., et al. Cell. 2020.
12. Ni L, Ye F, Cheng ML, et al. Immunity. 52(6):971977.e3. 2020.
13. Mu J, Xu J, Zhang L, et al. Sci China Life Sci. 14. 2020.