GTF2IRD1 antibody

GeneTex

GTF2IRD1 antibody

9

ImmunoFluorescence, Western Blot, ImmunoCytoChemistry

Research Use Only

Polyclonal

1.51 mg/ml

Unconjugated

GTF2IRD1

GTF2I repeat domain containing 1

BEN; binding factor for early enhancer; CREAM1; general transcription factor 3; general transcription factor III; general transcription factor II-I repeat domain-containing protein 1; GTF3; hMusTRD1alpha1; muscle TFII-I repeat domain-containing protein 1 alpha 1; MUSTRD1; RBAP2; slow-muscle-fiber enhancer-binding protein; USE B1-binding protein; WBS; WBSCR11; WBSCR12; williams-Beuren syndrome chromosomal region 12 protein; Williams-Beuren syndrome chromosome region 11

Rabbit

IgG

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]

Human

2°C to 8°C,-20°C or -80°C

12352203