GTF2IRD1 antibody

Cannot supply to this region.

SKU:: GTX131433
Additional Names:: GTF2I repeat domain containing 1 , BEN , CREAM1 , GTF3 , MUSTRD1 , RBAP2 , WBS , WBSCR11 , WBSCR12 , hMusTRD1alpha1
Application:: WB, IF, ICC
Concentration:: 1.51 mg/ml
Physical State:: Liquid
Species Reactivity:: Human
Purification:: Affinity Purified
Storage Conditions:: -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:: Genetex
Host:: Rabbit
Reactivities:: Human
Buffer:: PBS, 20% Glycerol, 0.025% ProClin 300.
Immunogen:: Recombinant protein encompassing a sequence within the center region of human GTF2IRD1. The exact sequence is proprietary.
Uniprot:: Q9UHL9
Synonyms:: BEN;binding factor for early enhancer;CREAM1;general transcription factor 3;general transcription factor II-I repeat domain-containing protein 1;general transcription factor III;GTF3;hMusTRD1alpha1;Muscle TFII-I repeat domain-containing protein 1;muscle TFII-I repeat domain-containing protein 1 alpha 1;MUSTRD1;MusTRD1/BEN;RBAP2;slow-muscle-fiber enhancer-binding protein;USE B1-binding protein;WBS;WBSCR11;WBSCR12;Williams-Beuren syndrome chromosomal region 11 protein;williams-Beuren syndrome chromosomal region 12 protein;Williams-Beuren syndrome chromosome region 11
Extra Details:: 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]

Shipping Conditions:: Blue Ice