GTF2IRD1 Antibody - C-terminal region
Artikelnummer:
ASB-ARP33735_T100
- Bilder (3)
| Artikelname: | GTF2IRD1 Antibody - C-terminal region |
| Artikelnummer: | ASB-ARP33735_T100 |
| Hersteller Artikelnummer: | ARP33735_T100 |
| Alternativnummer: | ASB-ARP33735_T100-25UL,ASB-ARP33735_T100-100UL |
| Hersteller: | Aviva |
| Wirt: | Rabbit |
| Kategorie: | Proteine/Peptide |
| Applikation: | IHC, WB |
| Spezies Reaktivität: | Bovine, Canine, Equine, Guinea pig, Human, Mouse, Rabbit, Rat |
| Immunogen: | The immunogen is a synthetic peptide directed towards the C terminal region of human GTF2IRD1 |
| Alternative Synonym: | BEN, WBS, GTF3, RBAP2, CREAM1, MUSTRD1, WBSCR11, WBSCR12, hMusTRD1alpha1 |
| GTF2IRD1 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. GTF2IRD1 is related to Williams-Beuren syndrome, a multisystem developmental disorder. Western blots using three different antibodies against three unique regions of this protein target confirm the same apparent molecular weight in our tests. 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. |
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Human kidney |
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WB Suggested Anti-GTF2IRD1 Antibody Titration: 2.5ug/ml Positive Control: Transfected 293T |
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GTF2IRD1 antibody - C-terminal region (ARP33735_T100) in Transfected 293T using Western Blot |
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