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WB analysis of various sample lysates using GTX64656 FGD4 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX64656 FGD4 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX64656 FGD4 antibody. Dilution : 1:1000 Loading : 25microg per lane

FGD4 antibody

GTX64656
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetFGD4
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Overview

  • Supplier
    GeneTex
  • Product Name
    FGD4 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID121512
  • Target name
    FGD4
  • Target description
    FYVE, RhoGEF and PH domain containing 4
  • Target synonyms
    actin-filament binding protein frabin; CMT4H; FGD1 family, member 4; FGD1-related F-actin-binding protein; FRABP; FYVE, RhoGEF and PH domain-containing protein 4; ZFYVE6; zinc finger FYVE domain-containing protein 6
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ96M96
  • Protein Name
    FYVE, RhoGEF and PH domain-containing protein 4
  • Scientific Description
    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. [provided by RefSeq, Jan 2015]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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