麻疹病毒融合蛋白F抗体

货号:bs-0886R
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概述

产品编号
bs-0886R
英文名称
MeV F Rabbit pAb
中文名称
麻疹病毒融合蛋白F抗体
英文别名
FUS_MEASE; F; MeVgp4; HEMA_MEASE; H; MeVgp5;
抗体来源
Rabbit
免疫原
KLH conjugated synthetic peptide derived from Measles virus fusion protein: 451-550/550
亚型
IgG
性状
Liquid
纯化方法
affinity purified by Protein A
克隆类型
Polyclonal
理论分子量
57 kDa
浓度
1mg/ml
储存液
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件
Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
产品介绍
麻疹病毒血凝素蛋白(Hemagglutinin protein,H)是介导麻疹病毒吸附、侵入宿主细胞的关键分子,麻疹病毒H蛋白在细胞膜上的表达,以及被麻疹病毒感染的细胞和未感染细胞的直接接触能够引起其受体CD46的表达下调.
背景资料
No data available.

产品应用

应用已检合格种属预测种属推荐稀释比例
ELISAMeasles virus1:5000-10000

交叉反应

交叉反应: (predicted: Measles virus)

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靶标

基因名
F
蛋白名
Fusion glycoprotein F0
亚基
Homotrimer of disulfide-linked F1-F2 (By similarity).
亚细胞定位
Virion. Host cytoplasm.
组织特异性
Virion membrane; Single-pass type I membrane protein. Host cell membrane; Single-pass membrane protein.
翻译后修饰
The inactive precursor F0 is glycosylated and proteolytically cleaved into F1 and F2 to be functionally active. The cleavage is mediated by cellular proteases during the transport and maturation of the polypeptide (By similarity).
相似性
Belongs to the paramyxoviruses fusion glycoprotein family.
功能
Class I viral fusion protein. Under the current model, the protein has at least 3 conformational states: pre-fusion native state, pre-hairpin intermediate state, and post-fusion hairpin state. During viral and plasma cell membrane fusion, the heptad repeat (HR) regions assume a trimer-of-hairpins structure, positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain. The formation of this structure appears to drive apposition and subsequent fusion of viral and plasma cell membranes. Directs fusion of viral and cellular membranes leading to delivery of the nucleocapsid into the cytoplasm. This fusion is pH independent and occurs directly at the outer cell membrane. The trimer of F1-F2 (F protein) probably interacts with H at the virion surface. Upon HN binding to its cellular receptor, the hydrophobic fusion peptide is unmasked and interacts with the cellular membrane, inducing the fusion between cell and virion membranes. Later in infection, F proteins expressed at the plasma membrane of infected cells could mediate fusion with adjacent cells to form syncytia, a cytopathic effect that could lead to tissue necrosis (By similarity).

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