GTF2IRD1 antibody

Cannot supply to this region.

SKU:: GTX33232
Additional Names:: GTF2I repeat domain containing 1 , BEN , CREAM1 , GTF3 , MUSTRD1 , RBAP2 , WBS , WBSCR11 , WBSCR12 , hMusTRD1alpha1
Application:: WB
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, Mouse, Rat
Buffer:: PBS, 50% Glycerol, 0.02% Sodium azide.
Immunogen:: Recombinant fusion protein containing a sequence corresponding to amino acids 660-959 of human GTF2IRD1 (NP_057412.1).
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 plays a role in craniofacial and cognitive development and mutations have been associated with Williams-Beuren syndrome, a multisystem developmental disorder caused by deletion of multiple genes at 7q11.23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2010]

Shipping Conditions:: Blue Ice