SARS Spike Protein (C-terminal) [GST] (DAG539)

Recombinant SARS Spike Protein (C-terminal) from E. coli [GST]

Product Overview
Recombinant SARS Coronavirus antigen (37 kDa), contains a mosaic of the immunodominant regions of the C-terminal of the Spike protein and a GST fusion partner, was expressed in Ecoli, and puried in vitro using Metal affinity chromatography techniques.
Nature
Recombinant
Tag/Conjugate
GST
Molecular Weight
37 kDa
Alternative Names
SARS Spike Protein; SARS; SARS S Protein; SARS Spike; SARS S
Procedure
None
Purity
> 95% pure (10% PAGE, coomassie staining). GS-4B Sepharose-Affinity Purification.
Format
Liquid
Concentration
1 mg/ml
Buffer
25mM Tris-HCl, 0.4% sarcosyl, 0.25% Triton-X100, 50% glycerol
Preservative
None
Storage
Upon receipt, store at -20°C
Introduction
The SARS coronavirus, sometimes shortened to SARS-CoV, is the virus that causes severe acute respiratory syndrome (SARS). On April 16, 2003, following the outbreak of SARS in Asia and secondary cases elsewhere in the world, the World Health Organization (WHO) issued a press release stating that the coronavirus identified by a number of laboratories was the official cause of SARS. Samples of the virus are being held in laboratories in New York, San Francisco, Manila, Hong Kong, and Toronto. protein E is a kinesin-like motor protein that accumulates in the G2 phase of the cell cycle. Unlike other centromere-associated proteins, it is not present during interphase and first appears at the centromere region of chromosomes during prometaphase. CENPE is proposed to be one of the motors responsible for mammalian chromosome movement and/or spindle elongation.
Keywords
SARS Spike Protein; SARS; SARS S Protein; SARS Spike; SARS S

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References


Hu, HB; Li, L; et al. Screening and identification of linear B-cell epitopes and entry-blocking peptide of severe acute respiratory syndrome (SARS)-associated coronavirus using synthetic overlapping peptide library. JOURNAL OF COMBINATORIAL CHEMISTRY 7:648-656(2005).
Rani, M; Bolles, M; et al. Increased Antibody Affinity Confers Broad In Vitro Protection against Escape Mutants of Severe Acute Respiratory Syndrome Coronavirus. JOURNAL OF VIROLOGY 86:9113-9121(2012).

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