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ZEBOV GP Antikörper

ZEBOV GP Reaktivität: Zaire ebolavirus ELISA Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7383906
  • Target Alle ZEBOV GP Produkte
    ZEBOV GP (Zaire Ebola Virus Envelope Glycoprotein (ZEBOV GP))
    Reaktivität
    Zaire ebolavirus
    Wirt
    • 1
    • 1
    Kaninchen
    Klonalität
    • 1
    • 1
    Polyklonal
    Konjugat
    • 2
    Dieser ZEBOV GP Antikörper ist unkonjugiert
    Applikation
    • 2
    • 1
    ELISA
    Spezifität
    Anti-Ebola virus EBOV(subtype Zaire, strain H.sapiens-wt/GIN/2014/Kissidougou-C15) Glycoprotein/GP Polyclonal Antibody
    Aufreinigung
    Antigen Affinity
    Immunogen
    Recombinant EBOV (subtype Zaire, strain H.sapiens-wt/GIN/2014/Kissidougou-C15) Glycoprotein / GP Protein (His Tag), ABIN7198910
    Isotyp
    IgG
  • Applikationshinweise
    ELISA 1:5000-1:10000
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • 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.
  • Target
    ZEBOV GP (Zaire Ebola Virus Envelope Glycoprotein (ZEBOV GP))
    Andere Bezeichnung
    ZEBOV Glycoprotein/GP (ZEBOV 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.
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