GTF2IRD1 (Human) IP-WB Antibody Pair

Catalog # H00009569-PW2

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Size:1 Set
Price: USD $ 607.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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Immunoprecipitation of GTF2IRD1 transfected lysate using rabbit polyclonal anti-GTF2IRD1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-GTF2IRD1.

  • Specification

    Product Description

    This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (84); Rat (86)

    Quality Control Testing

    Immunoprecipitation-Western Blot (IP-WB)

    Immunoprecipitation of GTF2IRD1 transfected lysate using rabbit polyclonal anti-GTF2IRD1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-GTF2IRD1.

    Supplied Product

    Antibody pair set content:
    1. Antibody pair for IP: rabbit polyclonal anti-GTF2IRD1 (300 ul)
    2. Antibody pair for WB: mouse purified polyclonal anti-GTF2IRD1 (50 ug)

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    Immunoprecipitation-Western Blot

  • Gene Info — GTF2IRD1

    Entrez GeneID

    9569

    Gene Name

    GTF2IRD1

    Gene Alias

    BEN, CREAM1, GTF3, MUSTRD1, RBAP2, WBS, WBSCR11, WBSCR12, hMusTRD1alpha1

    Gene Description

    GTF2I repeat domain containing 1

    Omim ID

    194050 604318

    Gene Ontology

    Hyperlink

    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

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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