SEBOV GP 抗体
The 兔 单克隆 anti-SEBOV GP antibody (Clone 106) (ABIN7383898) specifically detects SEBOV GP in ELISA 和 WB.
The antibody is reactive with Sudan ebolavirus samples.
产品编号 ABIN7383898
发货至:
中国
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北京 101111
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Quick Overview for SEBOV GP 抗体 (ABIN7383898)
抗原
SEBOV GP
(Sudan Ebola Virus Envelope Glycoprotein (SEBOV GP))
适用
Sudan ebolavirus
宿主
兔
克隆类型
单克隆
标记
This SEBOV GP antibody is un-conjugated
应用范围
ELISA, Western Blotting (WB)
克隆位点
106
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特异性
- Anti-Ebola virus EBOV(Subtype Sudan, strain Gulu) Glycoprotein/GP1(mucin domain deleted) Monoclonal Antibody
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纯化方法
- Protein A Affinity
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免疫原
- Recombinant EBOV (Subtype Sudan, strain Gulu) Glycoprotein / GP1 (mucin domain deleted) Protein (His Tag), ABIN7198917
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亚型
- IgG
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应用备注
- WB 1:1000-1:5000 ELISA 1:5000-1:10000
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限制
- 仅限研究用
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浓度
- 1 mg/mL
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缓冲液
- 0.2 μm filtered solution in PBS
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- SEBOV GP (Sudan Ebola Virus Envelope Glycoprotein (SEBOV GP))
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别名
- SEBOV Glycoprotein/GP1
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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.
抗原
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