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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. [provided by RefSeq
Specifications
Specifications
| Antigen | GTF2I |
| Applications | ELISA, Immunofluorescence, Immunohistochemistry (PFA fixed), Western Blot |
| Classification | Monoclonal |
| Clone | 3E2 |
| Conjugate | Unconjugated |
| Description | Mouse monoclonal antibody raised against a full length recombinant GTF2I. |
| Formulation | PBS with no preservative; pH 7.4 |
| Gene | GTF2I |
| Gene Accession No. | BC004472 |
| Gene Alias | BAP-135/BAP135/BTKAP1/DIWS/FLJ38776/FLJ56355/IB291/SPIN/TFII-I/WBS/WBSCR6 |
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