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WB analysis of various sample lysates using GTX33232 GTF2IRD1 antibody. The signal was developed with ECL plus-Enhanced. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX33232 GTF2IRD1 antibody. The signal was developed with ECL plus-Enhanced. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX33232 GTF2IRD1 antibody. The signal was developed with ECL plus-Enhanced. Dilution : 1:1000 Loading : 25microg per lane

GTF2IRD1 antibody

GTX33232
GeneTex
ApplicationsWestern Blot
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetGTF2IRD1
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Overview

  • Supplier
    GeneTex
  • Product Name
    GTF2IRD1 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 ID9569
  • Target name
    GTF2IRD1
  • Target description
    GTF2I repeat domain containing 1
  • Target synonyms
    BEN, CREAM1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1, general transcription factor II-I repeat domain-containing protein 1, USE B1-binding protein, Williams-Beuren syndrome chromosome region 11, binding factor for early enhancer, general transcription factor 3, general transcription factor III, muscle TFII-I repeat domain-containing protein 1 alpha 1, slow-muscle-fiber enhancer-binding protein, williams-Beuren syndrome chromosomal region 12 protein
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9UHL9
  • Protein Name
    General transcription factor II-I repeat domain-containing protein 1
  • Scientific Description
    The protein encoded by this gene contains five GTF2I-like repeats and each repeat possesses a potential helix-loop-helix (HLH) motif. It may have the ability to interact with other HLH-proteins and function as a transcription factor or as a positive transcriptional regulator under the control of Retinoblastoma protein. This gene plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]
  • Reactivity
    Human, Mouse, Rat
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203