WBSCR11 rabbit pAb
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WBSCR11 rabbit pAb
Background :
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]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 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],UniProt :
Q9UHL9Swiss Prot :
Q9UHL9Reactivity :
Human; Mouse; RatImmunogen :
The antiserum was produced against synthesized peptide derived from human GTF2IRD1. AA range:71-120Clonality :
PolyclonalSource :
RabbitApplications :
WB; IHC; IF; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. Not yet tested in other applications.Molecular Weight :
106kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
106kDFragment :
IgGSubcellular Location :
Nucleus.Other Product Names :
GTF2IRD1; CREAM1; GTF3; MUSTRD1; RBAP2; WBSCR11; WBSCR12; General transcription factor II-I repeat domain-containing protein 1; GTF2I repeat domain-containing protein 1; General transcription factor III; MusTRD1/BEN; Muscle TFII-I repeat doGene ID (Human) :
9569

