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A24506

GTF2IRD1 Rabbit polyclonal antibody

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£152.00

SKU:
A24506
Zusätzliche Namen:
BEN|CREAM1|GTF2I repeat domain containing 1|GTF2IRD1|GTF3|hMusTRD1alpha1|MUSTRD1|RBAP2|WBS|WBSCR11|WBSCR12
Anwendung:
ELISA, WB
Molekulargewicht:
130kDa
Spezies-Reaktivität:
Human
Aufreinigung:
Affinity Purified
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Abclonal
Host:
Rabbit
Reaktivitäten:
Rat
Immunogen:
Recombinant protein (or fragment).This information is considered to be commercially sensitive.
Formulierung:
Unmodified
Sequenz:
SLGFSPPALPPERDSGDPLVDESLKRQGFQENYDARLSRIDIANTLREQVQDLFNKKYGEALGIKYPVQVPYKRIKSNPGSVIIEGLPPGIPFRKPCTFGSQNLERILAVADKIKFTVTRPFQGLIPKPDEDDANRLGEKVILREQVKELFNEKYGEALGLNRPVLVPYKLIRDSPDAVEVTGLPDDIPFRNPNTYDIHRLEKILKAREHVRMVIINQLQPFAEICNDAKV
Uniprot:
Q9UHL9
Synonyme:
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
Weitere 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.
Versandbedingungen:
Blue Ice