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GTF2I (Human) Recombinant Protein (P02)

  • Catalog # : H00002969-P02
  • Visit Frequency :
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  • Specification
  • Product Description:
  • Human GTF2I full-length ORF (AAH04472, 1 a.a. - 274 a.a.) recombinant protein with GST-tag at N-terminal.
  • Sequence:
  • MAQVAMSTLPVEDEESSESRMVVTFLMSALESMCKELAKSKAEVACIAVYETDVFVVGTERGRAFVNTRKDFQKDFVKYCVEEEEKAAEMHKMKSTTQANRMSVDAVEIETLRKTVEDYFCFCYGKALGKSTVVPVPYEKMLRDQSAVVVQGLPEGVAFKHPENYDLATLKWILENKAGVSFIIKRPFLEPKKHVGGRVMVTDADRSILSPGGSCGPIKVKTEPTEDSGISLEMAAVTVKEESEDPDYYQYNIQGSHHSSEGNEGTEMEVPAEG
  • Host:
  • Wheat Germ (in vitro)
  • Theoretical MW (kDa):
  • 55.88
  • Purification:
  • Glutathione Sepharose 4 Fast Flow
  • Quality Control Testing:
  • 12.5% SDS-PAGE Stained with Coomassie Blue

    QC Testing of H00002969-P02
  • Storage Buffer:
  • 50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • Best use within three months from the date of receipt of this protein.
  • Applications
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Application Image
  • Enzyme-linked Immunoabsorbent Assay
  • Western Blot (Recombinant protein)
  • Antibody Production
  • Protein Array
  • Gene Information
  • Entrez GeneID:
  • 2969
  • Gene Name:
  • GTF2I
  • Gene Alias:
  • BAP-135,BAP135,BTKAP1,DIWS,FLJ38776,FLJ56355,IB291,SPIN,TFII-I,WBS,WBSCR6
  • Gene Description:
  • general transcription factor II, i
  • Gene Summary:
  • This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13 and 21. [provided by RefSeq
  • Other Designations:
  • BTK-associated protein, 135kD,Bruton tyrosine kinase-associated protein 135,Williams-Beuren syndrome chromosome region 6
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