Anti-SARS-CoV-2 Nucleocapsid (N) (Clone NP1-E9) - HRP

Referência LT7017-50

Tamanho : 50ug

Marca : Leinco Technologies

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AntiSARSCoV2 Nucleocapsid (N) (Clone NP1E9) – HRP

Product No.: LT7017

Product No.LT7017
Clone
NP1E9
Target
SARSCoV2 Nucleocapsid (N)
Product Type
Recombinant Monoclonal Antibody
Alternate Names
COV2NP1E9, SARSCoV2 Nucleocapsid, SARSCoV2 Nucleoprotein, Protein N, SARSCoV N Protein
Isotype
Human IgG1
Applications
ELISA

Data

AntiSARSCoV2 N (Clone NP1E9) Data Image

Antibody Details

Product Details

Reactive Species
SARSCoV2
Virus
Host Species
Mouse
Expression Host
HEK293 Cells
Immunogen
SARSCoV2 Nucleocapsid (N) Protein
Product Concentration
0.5 mg/ml
Formulation
This HRPconjugated antibody is formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 7.4, 1% BSA. (Warning: Use of sodium azide as a preservative will inhibit the enzyme activity of horseradish peroxidase)
Storage and Handling
This horseradish peroxidase conjugated monoclonal 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 NP1E9, 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 that belongs to the Coronaviridae family 1. 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, respectively 3, 4. The primary function of the N protein is to bind to and package the viral RNA genome into a helical ribonucleoprotein complex 5. The N protein is also involved in other critical steps of the viral life cycle, including transcription, replication, and modulating infected cell signaling pathways 6, 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 antibodies 8,9 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 SARSCoV2 12. The N protein also contributes to immune evasion by antagonizing antiviral RNAi 13, 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. Guo L., Ren L., Yang S., et al. Clinical Infectious Diseases: an Official Publication of the Infectious Diseases Society of America. 2020.
9. To K.K., Tsang O.T., Leung W.S., et al. Lancet Infect. Dis. 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. Mu J, Xu J, Zhang L, et al. Sci China Life Sci. 14. 2020.