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ZEBOV GP 抗体

This anti-ZEBOV GP antibody is a 小鼠 单克隆 antibody detecting ZEBOV GP in ELISA. Suitable for Zaire ebolavirus.
产品编号 ABIN7383905
发货至: 中国

Quick Overview for ZEBOV GP 抗体 (ABIN7383905)

抗原

ZEBOV GP (Zaire Ebola Virus Envelope Glycoprotein (ZEBOV GP))

适用

Zaire ebolavirus

宿主

  • 2
小鼠

克隆类型

  • 2
单克隆

标记

  • 2
This ZEBOV GP antibody is un-conjugated

应用范围

  • 2
  • 1
ELISA

克隆位点

2
  • 特异性

    Anti-Ebola virus EBOV(subtype Zaire, strain H.sapiens-wt/GIN/2014/Kissidougou-C15) Glycoprotein/GP Monoclonal Antibody

    纯化方法

    Protein A Affinity

    免疫原

    Recombinant EBOV (subtype Zaire, strain H.sapiens-wt/GIN/2014/Kissidougou-C15) Glycoprotein / GP Protein (His Tag), ABIN7198910

    亚型

    IgG1
  • 应用备注

    ELISA 1:1000-1:2000

    限制

    仅限研究用
  • 浓度

    1 mg/mL

    缓冲液

    0.2 μm filtered solution in PBS

    储存条件

    -20 °C

    储存方法

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

    ZEBOV GP (Zaire Ebola Virus Envelope Glycoprotein (ZEBOV GP))

    别名

    ZEBOV Glycoprotein/GP

    背景

    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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