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Invitrogen™ GTF2I Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA517642
Description
It is not recommended to aliquot this antibody.
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.
Specifications
GTF2I | |
Polyclonal | |
Unconjugated | |
GTF2I | |
6030441I21Rik; BAP135; BAP-135; Bruton tyrosine kinase-associated protein 135; BTKAP1; BTK-associated protein 135; BTK-associated protein, 135kD; DIWS; Diws1t; general transcription factor II I; general transcription factor IIi; general transcription factor II-I; Gtf2i; Gtf2ird1; GTFII-I; IB291; OTTHUMP00000209509; Spin; SRF-Phox1-interacting protein; tfiii; TFII-I; WBS; WBSCR6; Williams-Beuren syndrome chromosomal region 6 protein; Williams-Beuren syndrome chromosome region 6 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
14886, 2969 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot, Immunocytochemistry | |
15 μg/mL | |
0.01M HEPES with 100μg/mL BSA, 50% glycerol, 0.15M NaCl and no preservative; pH 7.5 | |
P78347, Q9ESZ8 | |
GTF2I | |
Synthetic peptide corresponding to residues of human TFII-I. | |
100 μL | |
Primary | |
Human, Mouse, Monkey | |
Antibody | |
IgG |
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