"GTF2I" Related Products

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Recombinant Human GTF2I cell lysate

Cat.No.: GTF2I-763HCL
Description: 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. Alternative splicing results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 7, 13 and 21.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: GTF2I general transcription factor IIi [ Homo sapiens ]
Official Symbol: GTF2I
Synonyms: GTF2I; general transcription factor IIi; general transcription factor II, i , WBSCR6; general transcription factor II-I; BAP 135; BTKAP1; DIWS; IB291; SPIN; TFII I; BTK-associated protein 135; BTK-associated protein, 135kD; SRF-Phox1-interacting protein; Williams-Beuren syndrome chromosome region 6; Bruton tyrosine kinase-associated protein 135; williams-Beuren syndrome chromosomal region 6 protein; WBS; BAP135; TFII-I; WBSCR6; GTFII-I; FLJ38776; FLJ56355;
Gene ID: 2969
mRNA Refseq: NM_001163636
Protein Refseq: NP_001157108
MIM: 601679
UniProt ID: P78347
Chromosome Location: 7q11.23
Pathway: B Cell Receptor Signaling Pathway, organism-specific biosystem; Basal transcription factors, organism-specific biosystem; Basal transcription factors, conserved biosystem; Herpes simplex infection, organism-specific biosystem; Herpes simplex infection, conserved biosystem; TNF-alpha/NF-kB Signaling Pathway, organism-specific biosystem;
Function: DNA binding; mitogen-activated protein kinase binding; protein binding; sequence-specific DNA binding transcription factor activity;

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