Anti-SARS-CoV-2 Spike NTD (Clone 2146) - HRP

Referência LT2010-50

Tamanho : 50ug

Marca : Leinco Technologies

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AntiSARSCoV2 Spike NTD (Clone 2146) – HRP

Product No.: LT2010

Product No.LT2010
Clone
2146
Target
SARSCoV2 Spike NTD
Product Type
Recombinant Monoclonal Antibody
Alternate Names
COV22146, SARSCoV2 Spike NTD, COVID19, 2019nCoV, Severe acute respiratory syndrome coronavirus 2, SARSCoV2
Isotype
Human IgG1
Applications
ELISA
,
IHC

Data

AntiSARS CoV2 NTD, Clone 2146 ELISA DataCoating: Purified Recombinant SARSCoV2 Spike NTD (Prod. No. S853) concentration of 1 ug/ml, 100 ul/well overnight at 28°C. Detection: AntiSARSCoV2 NTD (Clone 2146) conjugated to HRP was serially diluted starting at 25 ng/ml down to 0.23 ng/ml, 100 ul/well for 1 hour at 37°C. Substrate: TMB (Leinco T118), 100 ul/well for 15 min. at room temperature followed by Leinco 450 nm Stop Solution (Leinco T125), 50 ul/well.

Antibody Details

Product Details

Reactive Species
SARSCoV2
Virus
Expression Host
HEK293 Cells
Immunogen
Sequenced from human survivors of COVID19 (SARSCoV2)
Product Concentration
0.5 mg/ml
Formulation
This recombinant 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
Overnight on Blue Ice
Applications and Recommended Usage?
Quality Tested by Leinco
ELISA
Additional Applications Reported In Literature ?
IHC
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 Spike NTDHRP, clone 2146, specifically targets an epitope on the SARSCoV2 spike protein Nterminal domain.
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 S protein is a transmembrane, homotrimeric, class I fusion glycoprotein that mediates viral attachment, fusion, and entry into host cells 3. Each ~180 kDa monomer contains two functional subunits, S1 (~700 a.a) and S2 (~600 a.a), that mediate viral attachment and membrane fusion, respectively. S1 contains two major domains, the Nterminal (NTD) and Cterminal domains (CTD). In both SARSCoV and SARSCoV2, the CTD contains the receptorbinding domain (RBD), which binds to the angiotensinconverting enzyme 2 (ACE2) receptor on host cells35. The NTD of SARSCoV2 does not bind to ACE26, and the function of NTD in SARSCoV2 infection is not well understood. In other CoVs, the NTD may promote attachment by binding to sugar moieties7 and might play a role in the conformational change of S2 required for membrane fusion8. While most neutralizing antibodies target the RBD domain and block receptor binding, potent neutralizing antibodies targeting NTD were isolated from convalescent COVID19 patients9, identifying the NTD as an attractive candidate for vaccines and therapeutics. In addition, the NTD is a promising antigen for diagnostic tests, as there is only 53.5% homology between the NTD of SARSCoV2 and SARSCoV10.
Antigen Distribution
The spike NTD is expressed on the surface 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. Wrapp D, Wang N, Corbett KS, et al. bioRxiv. 2020.
4. Walls AC, Park YJ, Tortorici MA, et al. Cell. 181(2):281292.e6. 2020.
5. Li W, Zhang C, Sui J, et al. EMBO J. 24(8):16341643. 2020.
6. Wang Q, Zhang Y, Wu L, et al. Cell. 181(4):894904.e9. 2020.
7. Park, Y., Walls, A.C., Wang, Z. et al. Nat Struct Mol Biol 26, 1151–1157. 2019.
8. Zhou, H., Chen, Y., Zhang, S. et al. Nat Commun 10, 3068. 2019.
9. Chi X, Yan R, Zhang J, et al. Science. eabc6952. 2020.
10. Ou, X., Liu, Y., Lei, X. et al. Nat Commun 11, 1620. 2020.

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