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IHC analysis of mouse skeletal muscle (first panel, and in green in third panel) using GTX88050 MYO5A antibody, Internal. Alpha-bungaratoxin staining in middle panel and in red in third panel. Dilution : 1microg/ml
IHC analysis of mouse skeletal muscle (first panel, and in green in third panel) using GTX88050 MYO5A antibody, Internal. Alpha-bungaratoxin staining in middle panel and in red in third panel. Dilution : 1microg/ml
IHC analysis of mouse skeletal muscle (first panel, and in green in third panel) using GTX88050 MYO5A antibody, Internal. Alpha-bungaratoxin staining in middle panel and in red in third panel. Dilution : 1microg/ml

MYO5A antibody, Internal

GTX88050
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry
DownloadDatasheet
Product group Antibodies
ReactivityHuman, Mouse
TargetMYO5A
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Overview

  • Supplier
    GeneTex
  • Product Name
    MYO5A antibody, Internal
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody is expected to recognize both reported isoforms (NP_000250.3; NP_001135967.1).
  • Application Supplier Note
    WB: 1-3microg/ml. IHC: 1-3microg/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.50 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4644
  • Target name
    MYO5A
  • Target description
    myosin VA
  • Target synonyms
    dilute myosin heavy chain, non-muscle; GS1; MYH12; MYO5; myosin V; myosin VA (heavy chain 12, myoxin); myosin, heavy polypeptide kinase; myosin-12; myosin-Va; myoxin; MYR12; unconventional myosin-Va
  • Host
    Goat
  • Isotype
    IgG
  • Protein IDQ9Y4I1
  • Protein Name
    Unconventional myosin-Va
  • Scientific Description
    This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq, Dec 2008]
  • Reactivity
    Human, Mouse
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203