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FGD4 抗体 (AA 99-198)

This anti-FGD4 antibody is a 兔 多克隆 antibody detecting FGD4 in WB. Suitable for 人.
产品编号 ABIN6140588
发货至: 中国

Quick Overview for FGD4 抗体 (AA 99-198) (ABIN6140588)

抗原

See all FGD4 抗体
FGD4 (FYVE, RhoGEF and PH Domain Containing 4 (FGD4))

适用

  • 18
  • 2
  • 2

宿主

  • 18

克隆类型

  • 18
多克隆

标记

  • 13
  • 1
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  • 1
This FGD4 antibody is un-conjugated

应用范围

  • 17
  • 8
  • 2
  • 2
  • 2
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  • 2
  • 1
  • 1
Western Blotting (WB)
  • 抗原表位

    • 8
    • 3
    • 2
    • 2
    • 1
    AA 99-198

    序列

    QMECEEEKAA TLSSDTSIQA SEPLLDTHIV NGERDETATA PASPTTDSCD GNASDSSYRT PGIGPVLPLE ERGAETETKV QERENGESPL ELEQLDQHHE

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 99-198 of human FGD4 (NP_640334.2).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000

    说明

    HIGH QUALITY

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

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

    FGD4 (FYVE, RhoGEF and PH Domain Containing 4 (FGD4))

    别名

    FGD4

    背景

    This gene encodes a protein that is involved in the regulation of the actin cytoskeleton and cell shape. This protein contains an actin filament-binding domain, which together with its Dbl homology domain and one of its pleckstrin homology domains, can form microspikes. This protein can activate MAPK8 independently of the actin filament-binding domain, and it is also involved in the activation of CDC42 via the exchange of bound GDP for free GTP. The activation of CDC42 also enables this protein to play a role in mediating the cellular invasion of Cryptosporidium parvum, an intracellular parasite that infects the gastrointestinal tract. Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H), a disorder of the peripheral nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.,FGD4,CMT4H,FRABP,ZFYVE6,FYVE,FGD4

    分子量

    20 kDa/32 kDa/86 kDa

    基因ID

    121512

    UniProt

    Q96M96

    途径

    Neurotrophin Signaling Pathway
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