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WB analysis of HeLa cell lysate (in RIPA buffer) using GTX13703 MITF antibody [21D1418]. Loading : 35μg Dilution : 0.1μg/ml
WB analysis of HeLa cell lysate (in RIPA buffer) using GTX13703 MITF antibody [21D1418]. Loading : 35μg Dilution : 0.1μg/ml
WB analysis of HeLa cell lysate (in RIPA buffer) using GTX13703 MITF antibody [21D1418]. Loading : 35μg Dilution : 0.1μg/ml

MITF antibody [21D1418]

GTX13703
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetMITF
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Overview

  • Supplier
    GeneTex
  • Product Name
    MITF antibody [21D1418]
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.1 - 1 microg/ml. ICC/IF: 1-5 microg/ml. IHC-P: 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    21D1418
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID4286
  • Target name
    MITF
  • Target description
    melanocyte inducing transcription factor
  • Target synonyms
    CMM8, COMMAD, MI, MITF-A, WS2, WS2A, bHLHe32, microphthalmia-associated transcription factor, class E basic helix-loop-helix protein 32, melanogenesis associated transcription factor, microphtalmia-associated transcription factor
  • Host
    Mouse
  • Isotype
    IgG1
  • Protein IDO75030
  • Protein Name
    Microphthalmia-associated transcription factor
  • Scientific Description
    This gene encodes a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. It regulates the differentiation and development of melanocytes retinal pigment epithelium and is also responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    41116161