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Description
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. Synonyms: Monoclonal GTF2IRD1 antibody, Anti-GTF2IRD1 antibody, General transcription factor II-I repeat domain-containing protein 1 antibody, GTF3 antibody, RBAP2 antibody, CREAM1 antibody, MUSTRD1 antibody, WBSCR11 antibody, WBSCR12 antibody, hMusTRD1alpha1 antibody.
Immunogen
GTF2 IRD1 antibody was raised in mouse using recombinant Gtf2 Repeat Domain Containing 1 (Gtf2 rd1)