GTF2I is a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon(s) encoding 5 UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 transcript variants.
WB Suggested Anti-GTF2I Antibody Titration: 0.2-1 ug/mlELISA Titer: 1:312500Positive Control: HepG2There is BioGPS gene expression data showing that GTF2I is expressed in HepG2
WB Suggested Anti-GTF2I Antibody Titration: 2.5 ug/ml Positive Control: HepG2 Whole CellThere is BioGPS gene expression data showing that GTF2I is expressed in HepG2
GTF2I antibody - N-terminal region (ARP31910_T100) in Human HepG2 using Western Blot
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