GTF2H2 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00002966-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

GTF2H2 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: GTF2H2 transfected lysate ( 43.56 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-GTF2H2 full-length

    Host

    Human

    Theoretical MW (kDa)

    43.56

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-GTF2H2 antibody (H00002966-B01) by Western Blots.

    SDS-PAGE Gel

    GTF2H2 transfected lysate.

    Western Blot

    Lane 1: GTF2H2 transfected lysate ( 43.56 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 — GTF2H2

    Entrez GeneID

    2966

    GeneBank Accession#

    NM_001515.2

    Protein Accession#

    -

    Gene Name

    GTF2H2

    Gene Alias

    BTF2, BTF2P44, MGC102806, T-BTF2P44, TFIIH

    Gene Description

    general transcription factor IIH, polypeptide 2, 44kDa

    Omim ID

    601748

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is within the telomeric copy of the duplication. Deletion of this gene sometimes accompanies deletion of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients but it is unclear if deletion of this gene contributes to the SMA phenotype. This gene encodes the 44 kDa subunit of RNA polymerase II transcription initiation factor IIH which is involved in basal transcription and nucleotide excision repair. Transcript variants for this gene have been described, but their full length nature has not been determined. A second copy of this gene within the centromeric copy of the duplication has been described in the literature. It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the centromeric copy of the gene. [provided by RefSeq

    Other Designations

    general transcription factor IIH, polypeptide 2 (44kD subunit)|general transcription factor IIH, polypeptide 2, 44kD subunit

  • 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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