GTF2IRD1 Antibody


Western Blot: GTF2IRD1 Antibody [NB100-92409] - Analysis of GTF2IRD1 antibody at 1:500 dilution. Lane 1 - HEK293T whole cell lysate, Lane 2 - Raw264.7 whole cell lysate, Lane 3 - H9C2 whole cell lysate.

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GTF2IRD1 Antibody Summary

Synthetic peptide, corresponding to amino acids 63-112 of Human WBSCR11.
GTF2IRD1 antibody detects endogenous levels of human GTF2I repeat domain-containing protein.
Immunogen affinity purified
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  • Western Blot 1:500-1:1000
Theoretical MW
106 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Positive Control
GTF2IRD1 Lysate (NBL1-11393)

Packaging, Storage & Formulations

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.
PBS (pH 7.2)
0.05% Sodium Azide
1.0 mg/ml
Immunogen affinity purified

Alternate Names for GTF2IRD1 Antibody

  • BEN
  • CREAM1
  • general transcription factor II-I repeat domain-containing protein 1
  • General transcription factor III
  • GTF2I repeat domain containing 1
  • GTF2I repeat domain-containing protein 1
  • GTF3GTF2I repeat domain-containing 1
  • hMusTRD1alpha1
  • muscle TFII-I repeat domain-containing protein 1 alpha 1
  • Muscle TFII-I repeat domain-containing protein 1
  • MusTRD1
  • MusTRD1/BEN
  • MUSTRD1general transcription factor 3
  • RBAP2WBSCR12binding factor for early enhancer
  • Slow-muscle-fiber enhancer-binding protein
  • USE B1-binding protein
  • WBS
  • WBSCR11
  • Williams-Beuren syndrome chromosomal region 11 protein
  • Williams-Beuren syndrome chromosomal region 12 protein
  • Williams-Beuren syndrome chromosome region 11


Williams-Beuren syndrome (WBS) is a developmental disorder caused by the hemizygous microdeletion on chromosome 7q11.23. WBS is an autosomal dominant genetic condition that is characterized by physical, cognitive and behavioral traits. The physical traits associated with WBS include facial dysmorphology, vascular stenoses, growth deficiencies, dental anomalies and neurologic and musculoskeletal abnormalities. Mild retardation, a weakness in visual-spatial skills, anxiety and a short attention span are typical cognitive and behavioral traits of WBS patients. The WBSCR11 gene is located within the WBS deletion and may contribute to the developmental symptoms found in WBS because of a loss of the encoded transcription factor. WBSCR11 is also designated GRF2IRD1, GTF3, Cream1 and MusTRD1 in human and BEN in mouse, due to slight differences in gene structure. WBSCR11 is expressed in all adult tissues as several variants and has discrete spatial and temporal expression during embryogenesis. The amino-terminus of WBSCR11 interacts with transcriptional machinery proteins, while the carboxy-terminus has been shown to bind the retinoblastoma protein to possibly regulate the cell cycle.


This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Positive Control Lysate(s)

Secondary Antibodies


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Gene Symbol GTF2IRD1