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GTF2IRD1 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00009569-T01
  • Visit Frequency :
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-GTF2IRD1 full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 106
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-GTF2IRD1 antibody (H00009569-B01) by Western Blots.
    SDS-PAGE Gel
    QC Testing of H00009569-T01
    GTF2IRD1 transfected lysate.
    Western Blot
    QC Testing of H00009569-T01
    Lane 1: GTF2IRD1 transfected lysate ( 106 KDa)
    Lane 2: Non-transfected lysate.
  • Storage Buffer:
  • 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Application Image
  • Western Blot
  • Gene Information
  • Entrez GeneID:
  • 9569
  • Protein Accession#:
  • -
  • Gene Name:
  • GTF2IRD1
  • Gene Alias:
  • BEN,CREAM1,GTF3,MUSTRD1,RBAP2,WBS,WBSCR11,WBSCR12,hMusTRD1alpha1
  • Gene Description:
  • GTF2I repeat domain containing 1
  • Gene Summary:
  • 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 is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing of this gene generates at least 2 transcript variants. [provided by RefSeq
  • Other Designations:
  • GTF2I repeat domain-containing 1,Williams-Beuren syndrome chromosome region 11,binding factor for early enhancer,general transcription factor 3,muscle TFII-I repeat domain-containing protein 1 alpha 1
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