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GTF2IRD1 polyclonal antibody

  • Catalog # : PAB7077
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of GTF2IRD1.
  • Immunogen:
  • A synthetic peptide corresponding to human GTF2IRD1.
  • Sequence:
  • C-NKFTKDTTKLEPAS
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 106
  • Specificity:
  • This antibody is expected to recognize both reported isoforms (NP_057412.1 and NP_005676.2).
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:64000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • Storage Instruction:
  • Store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Publication Reference
  • 1.
  • GTF2IRD1 in craniofacial development of humans and mice.
    Tassabehji M, Hammond P, Karmiloff-Smith A, Thompson P, Thorgeirsson SS, Durkin ME, Popescu NC, Hutton T, Metcalfe K, Rucka A, Stewart H, Read AP, Maconochie M, Donnai D.Science. 2005 Nov 18;310(5751):1184-7. Epub 2005 Nov 3.
  • Applications
  • ELISA
  • Application Image
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 9569
  • Protein Accession#:
  • NP_057412.1;NP_005676.2
  • 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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