SARS-CoV-2 Spike Protein (RBD) (E2T6M) Mouse Monoclonal Antibody#69323,Cell Signaling Technology (CST),69323

SARS-CoV-2 Spike Protein (RBD) (E2T6M) Mouse Monoclonal Antibody recognizes endogenous levels of total SARS-CoV-2 spike protein. This antibody detects full-length protein, and also detects the S1 fragment generated by furin cleavage. This antibody does not cross-react with spike proteins from SARS or MERS coronaviruses.

Host

Mouse

Reactivity

Virus

Application

Western Blotting: 1:1000

Platform ID

BAB756393752

Cell Signaling Technology (CST)

Headquarters

3 Trask Lane Danvers, MA 01923

Contact

Tel: 877-616-2355,978-867-2388
Fax: 877-616-2355

Product Specifications
Scientific Background
Synonyms

Specifications

NameSARS-CoV-2 Spike Protein (RBD) (E2T6M) Mouse Monoclonal Antibody#69323
Cat. No.69323
Accession NumberP0DTC2, 437405
Gene ID (Entrez)43740568
HostMouse
SensitivityEndogenous
ReactivityVirus
ApplicationWestern Blotting: 1:1000
Molecular Weight110, 220
ImmunogenIgG1
FormulationSupplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C.Do not aliquot the antibody.
StorageSupplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C.Do not aliquot the antibody.
Regulatory StatusResearch Use Only

Scientific Background

The cause of the COVID-19 pandemic is a novel and highly pathogenic coronavirus, termed SARS-CoV-2 (severe acute respiratory syndrome coronavirus-2). SARS-CoV-2 is a member of the Coronaviridae family of viruses (1). The genome of SARS-CoV-2 is similar to other coronaviruses, and is comprised of four key structural proteins: S, the spike protein, E, the envelope protein, M, the membrane protein, and N, the nucleocapsid protein (2). Coronavirus spike proteins are class I fusion proteins and harbor an ectodomain, a transmembrane domain, and an intracellular tail (3,4). The highly glycosylated ectodomain projects from the viral envelope surface and facilitates attachment and fusion with the host cell plasma membrane. The ectodomain can be further subdivided into host receptor-binding domain (RBD) (S1) and membrane-fusion (S2) subunits, which are produced upon proteolysis by host proteases at S1/S2 and S2’ sites. S1 and S2 subunits remain associated after cleavage and assemble into crown-like homotrimers (2,4). In humans, both SARS-CoV and SARS-CoV-2 spike proteins utilize the angiotensin-converting enzyme 2 (ACE2) protein as a receptor for cellular entry (5-7). Spike protein subunits represent a key antigenic feature of coronavirus virions, and therefore represent an important target of vaccines, novel therapeutic antibodies, and small-molecule inhibitors (8,9).Zhou, P. et al. (2020)Nature579, 270-3.Tortorici, M.A. and Veesler, D. (2019)Adv Virus Res105, 93-116.Li, F. et al. (2006)J Virol80, 6794-800.Li, F. (2016)Annu Rev Virol3, 237-61.Shang, J. et al. (2020)Nature581, 221-4.Wrapp, D. et al. (2020)Science367, 1260-3.Yan, R. et al. (2020)Science367, 1444-8.Yuan, Y. et al. (2017)Nat Commun8, 15092.Amanat, F. and Krammer, F. (2020)Immunity52, 583-9.Alternate Names2019-nCoV surface glycoprotein; Peplomer protein; S glycoprotein; SARS-CoV-2 spike protein; spike glycoprotein; SPIKE_SARS2; surface glycoprotein

Synonyms

2019-nCoV surface glycoprotein; Peplomer protein; S glycoprotein; SARS-CoV-2 spike protein; spike glycoprotein; SPIKE_SARS2; surface glycoprotein

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