产品名称 GTF2IRD1 Antibody from ABBEXA
产品货号 abx005071
产品价格 现货询价,电话:010-67529703
产品规格 50 µl, 100 µl, 200 µl
产品品牌 ABBEXA
产品概述
产品详情
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Antigenic SpecificityGTF2IRD1
Clonepolyclonal
Host SpeciesRabbit
Reactive Specieshuman, mouse, rat
Isotypen/a
Formataffinity purified
Size50 µl, 100 µl, 200 µl
Concentration> 1 mg/ml
ApplicationsWB. RUO
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DescriptionGTF2IRD1 Antibody is a Rabbit Polyclonal antibody against GTF2IRD1. 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.
ImmunogenRecombinant protein of human GTF2IRD1.
Other NamesBEN; WBS; GTF3; RBAP2; CREAM1; MUSTRD1; WBSCR11; WBSCR12; hMusTRD1alpha1; G2D1; GT2D1; GTF2I repeat domain containing protein 1; GTF2IRD1; General transcription factor II-I repeat domain-containing protein 1; General transcription factor III; MusTRD1/BEN; Muscle TFII-I repeat domain-containing protein 1; Slow- muscle-fiber enhancer binding protein; USE B1 binding protein; Williams-Beuren syndrome chromosome region 11 protein; GTF2I repeat domain-containing protein 1; Slow-muscle-fiber enhancer-binding protein; USE B1-binding protein; Williams-Beuren syndrome chromosomal region 11 protein; Williams-Beuren syndrome chromosomal region 12 protein; GTF2I repeat domain containing 1; HGNC:4661; GTF2I repeat domain-containing 1; Williams-Beuren syndrome chromosome region 11; general transcription factor 3; muscle TFII-I repeat
Gene, Accession #GTF2IRD1, Gene ID: 9569, SwissProt: Q9UHL9
Catalog #abx005071
Price
Order / More InfoGTF2IRD1 Antibody from ABBEXA
Product Specific Referencesn/a
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