GTF2IRD1 polyclonal antibody

Catalog # PAB7077

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Size:100 ug
Price: USD $ 428.00
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  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • 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.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — GTF2IRD1

    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

    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
  • Publication Reference
    • 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; 310(5751):1184.

      Application:WB-Ti, Human, HEK-293T cells.

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