The human Williams Syndrome Transcription Factor (WSTF) gene is located within the common Williams Syndrome deletion area at chromosome 7q11.23. Its Fn motifs include a PHD zinc finger motif followed by a bromodomain.
| Inventor | Institute |
|---|---|
| Patrick Varga-Weisz | Marie Curie Research Institute |
| SKU: | 151586 |
|---|---|
| Product description: | The human Williams Syndrome Transcription Factor (WSTF) gene is located within the common Williams Syndrome deletion area at chromosome 7q11.23. Its functional motifs include a PHD zinc finger motif followed by a bromodomain. Both motifs are found in many transcription factors, suggesting that WSTF may function as a transcription factor. WSTF forms a chromatinremodelling complex that mobilizes nucleosomes and reconfigures irregular chromatin to a regular nucleosomal array structure. The droso… |
| Conjugation: | Unconjugated |
| Molecular weight: | 170 kDa |
| Immunogen: | Peptide coupled to keyhole limpet hemocyanin. |
| Cat. #: | 151586 |
|---|---|
| Tool sub type: | Primary antibody |
| Unit size: | 100 ug |
| Cancer types: | Breast cancer |
| Research Fields: | Genetics |
| Application: | IF ; IP ; WB |
| Target: | Williams Syndrome Transcription Factor (WSTF) |
| Reactivity: | Human ; Mouse |
| Clone: | WSTF |
| Host: | Rabbit |
| Class: | Polyclonal |
| Target background: | The human Williams Syndrome Transcription Factor (WSTF) gene is located within the common Williams Syndrome deletion area at chromosome 7q11.23. Its Fn motifs include a PHD zinc finger motif followed by a bromodomain. Both motifs are found in many transcription factors, suggesting that WSTF may function as a transcription factor. WSTF forms a chromatinremodelling complex that mobilizes nucleosomes and reconfigures irregular chromatin to a regular nucleosomal array structure. The drosophila Ac… |
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| Format: | Liquid |
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| Concentration: | 0.9-1.1 mg/ml |
| Storage buffer: | Whole serum |
| Storage conditions: | -80° C |
| Shipping conditions: | Dry ice |
| References: |
Sarshad et al. 2013. PLoS Genet. 9(3):e1003397. PMID: 23555303. Nuclear myosin 1c facilitates the chromatin modifications required to activate rRNA gene transcription and cell cycle progression. Bozhenok et al. 2002. EMBO J. 21(9):2231-41. PMID: 11980720. WSTF-ISWI chromatin remodeling complex targets heterochromatic replication foci. |
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