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IP analysis of HeLa cell lysate using GTX55718 MYH9 antibody. Antibody amount : 3microg / 300microg lysate Dilution : 1:1000
IP analysis of HeLa cell lysate using GTX55718 MYH9 antibody. Antibody amount : 3microg / 300microg lysate Dilution : 1:1000
IP analysis of HeLa cell lysate using GTX55718 MYH9 antibody. Antibody amount : 3microg / 300microg lysate Dilution : 1:1000

MYH9 antibody

GTX55718
GeneTex
ApplicationsImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetMYH9
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Overview

  • Supplier
    GeneTex
  • Product Name
    MYH9 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:1000 - 1:2000. IHC-P: 1:50 - 1:100. IP: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoPrecipitation, Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID4627
  • Target name
    MYH9
  • Target description
    myosin heavy chain 9
  • Target synonyms
    BDPLT6, DFNA17, EPSTS, FTNS, MATINS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA, myosin-9, cellular myosin heavy chain, type A, myosin, heavy chain 9, non-muscle, non-muscle myosin heavy chain 9, non-muscle myosin heavy chain A, non-muscle myosin heavy chain IIa, non-muscle myosin heavy polypeptide 9, nonmuscle myosin IIA2, nonmuscle myosin heavy chain II-A
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP35579
  • Protein Name
    Myosin-9
  • Scientific Description
    This gene encodes a conventional non-muscle myosin; this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness. [provided by RefSeq, Dec 2011]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203