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GTF2I, Mouse, Polyclonal Antibody, Abnova™
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 | Immunofluorescence, Western Blot |
| Classification | Polyclonal |
| Conjugate | Unconjugated |
| Description | Mouse polyclonal antibody raised against a full-length human GTF2I protein. |
| Formulation | No additive |
| Gene | GTF2I |
| Gene Accession No. | BC099907.1 |
| Gene Alias | BAP-135/BAP135/BTKAP1/DIWS/FLJ38776/FLJ56355/IB291/SPIN/TFII-I/WBS/WBSCR6 |
| Gene Symbols | GTF2I |
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