GTF2IRD1 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00009569-T01

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Size:100 uL
Price: USD $ 247.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

GTF2IRD1 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: GTF2IRD1 transfected lysate ( 106 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-GTF2IRD1 full-length

    Host

    Human

    Theoretical MW (kDa)

    106

    Interspecies Antigen Sequence

    Mouse (84); Rat (86)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-GTF2IRD1 antibody (H00009569-B01) by Western Blots.

    SDS-PAGE Gel

    GTF2IRD1 transfected lysate.

    Western Blot

    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

  • Gene Info — GTF2IRD1

    Entrez GeneID

    9569

    GeneBank Accession#

    BC018136.1

    Protein Accession#

    -

    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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