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SEBOV GP antibody

This anti-SEBOV GP antibody is a Rabbit Monoclonal antibody detecting SEBOV GP in ELISA and WB. Suitable for Sudan ebolavirus.
Catalog No. ABIN7383898

Quick Overview for SEBOV GP antibody (ABIN7383898)

Target

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

Reactivity

Sudan ebolavirus

Host

  • 1
Rabbit

Clonality

  • 1
Monoclonal

Conjugate

  • 1
This SEBOV GP antibody is un-conjugated

Application

ELISA, Western Blotting (WB)

Clone

106
  • Specificity

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

    Purification

    Protein A Affinity

    Immunogen

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

    Isotype

    IgG
  • Application Notes

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

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    0.2 μm filtered solution in PBS

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

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

    Alternative Name

    SEBOV Glycoprotein/GP1

    Background

    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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