L’anticorps anti-SARS-CoV-2 Spike Monoclonal produit chez le Souris a été validé pour ELISA. Il convient pour la détection de SARS-CoV-2 Spike dans des échantillons provenant de SARS Coronavirus-2 (SARS-CoV-2).
}
S Recombinant Monoclonal Antibody, FITC conjugated
Attributs du produit
Recombinant anti-SARS-CoV-2 spike Mouse ScFv is expressed from 293 cells (HEK293) with a human IgG1 Fc tag on C-terminal. Mouse scFv fusion with human IgG1 Fc AA 16-685
Purification
Affinity-chromatography
Immunogène
Recombinant Human Novel Coronavirus Spike glycoprotein (S) (16-685aa) (CSB-MP3324GMY)
SARS-CoV-2 S
Reactivité: SARS Coronavirus-2 (SARS-CoV-2)
ELISA, Neut, GICA
Hôte: Human
Monoclonal
A1
Fc Tag
single-domain Antibody (sdAb)
Recombinant Antibody
This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Stock
-20 °C,-80 °C
Stockage commentaire
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze
Antigène
SARS-CoV-2 Spike (SARS-CoV-2 S)
Autre désignation
SARS-CoV-2 (SARS-CoV-2/ 2019-nCoV) S
Classe de substances
Viral Protein
Sujet
Spike glycoprotein comprises two functional subunits responsible for binding to the host cell receptor (S1 subunit) and fusion of the viral and cellular membranes (S2 subunit). For many coronavirus (CoVs), S is cleaved at the boundary between the S1 and S2 subunits, which remain non-covalently bound in the prefusion conformation. The distal S1 subunit comprises the receptor-binding domain(s) and contributes to stabilization of the prefusion state of the membrane-anchored S2 subunit that contains the fusion machinery. S is further cleaved by host proteases at the so-called S2' site located immediately upstream of the fusion peptide in all CoVs. This cleavage has been proposed to activate the protein for membrane fusion via extensive irreversible conformational changes. However, different CoVs use distinct domains within the S1 subunit to recognize a variety of attachment and entry receptors, depending on the viral species. Endemic human coronaviruses OC43 and HKU1 attach via their S domain A to 5-N-acetyl-9-O-acetyl-sialosides found on glycoproteins and glycolipids at the host cell surface to enable entry into susceptible cells. MERS-CoV S uses domain A to recognize non-acetylated sialoside attachment receptors, which likely promote subsequent binding of domain B to the entry receptor, dipeptidyl-peptidase 4. SARS-CoV and several SARS-related coronaviruses (SARSr-CoV) interact directly with angiotensin-converting enzyme 2 (ACE2) via SB to enter target cells.