SEBOV GP Antikörper

Produktnummer ABIN7383898

Produktdetails anti-SEBOV GP Antikörper

Target: SEBOV GP (Sudan Ebola Virus Envelope Glycoprotein (SEBOV GP))

Reaktivität: Sudan ebolavirus

Wirt: Kaninchen

Klonalität: Monoklonal

Konjugat: Dieser SEBOV GP Antikörper ist unkonjugiert

Applikation: ELISA, Western Blotting (WB)

Spezifität: Anti-Ebola virus EBOV(Subtype Sudan, strain Gulu) Glycoprotein/GP1(mucin domain deleted) Monoclonal Antibody

Aufreinigung: Protein A Affinity

Immunogen: Recombinant EBOV (Subtype Sudan, strain Gulu) Glycoprotein / GP1 (mucin domain deleted) Protein (His Tag), ABIN7198917

Klon: 106

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:1000-1:5000 ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 1 mg/mL

Buffer: 0.2 μm filtered solution in PBS

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu SEBOV GP

Target: SEBOV GP (Sudan Ebola Virus Envelope Glycoprotein (SEBOV GP))

Andere Bezeichnung: SEBOV Glycoprotein/GP1 (SEBOV GP Produkte)

Hintergrund: Glycoprotein,GP,The fourth gene of the EBOV genome encodes a 16- kDa envelope-attached glycoprotein (GP) and a 11 kDa secreted glycoprotein (sGP). Both GP and sGP have an identical 295-residue N-terminus, however, they have different C-terminal sequences. Recently, great attention has been paid to GP for vaccines design and entry inhibitors isolation. GP is a class I fusion protein which assembles as trimers on viral surface and plays an important role in virus entry and attachment. Mature GP is a disulfide-linked heterodimer formed by two subunits, GP1 and GP2, which are generated from the proteolytical process of GP precursor (pre-GP) by cellular furin during virus assembly . The GP1 subunit contains a mucin domain and a receptor-binding domain (RBD), the GP2 subunit has a fusion peptide, a helical heptad-repeat (HR) region, a transmembrane (TM) domain, and a 4-residue cytoplasmic tail. The RBD of GP1 mediates the interaction of EBOV with cellular receptor (e.g. DC-SIGN/LSIGN, TIM-1, hMGL, NPC1, β-integrins, folate receptor-α, and Tyro3 family receptors), of which TIM1 and NPC1 are essential for EBOV entry, the mucin domain having N- and O-linked glycans enhances the viral attachment to cellular hMGL, and participates in shielding key neutralization epitopes, which helps the virus evades immune elimination. There are large conformation changes of GP2 during membrane fusion, which enhance the insertion of fusion loop into cellular membrane and facilitate the release of viral nucleocapsid core to cytoplasm.