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Anti-WSTF, Polyclonal [WSTF]

Info

Catalogue Number 151586
Applications IF IP WB
Antigen/Gene or Protein Targets Williams Syndrome Transcription Factor (WSTF)
Reactivity Human and Mouse
Relevance 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 drosophila Acf1 gene is structurally related to the human WSTF gene.
Host Rabbit
Immunogen Peptide coupled to keyhole limpet hemocyanin.
Formulation Whole serum
Molecular Weight (kDa) 170
Notes Suggested dilutions for western blot: 1:2000
Positive Control ES, NIH 3T3, and HeLa cells
Research Area Epigenetics & Nuclear Signalling

References: 2 entries

Sarshad et al. 2013. PLoS Genet. 9(3):e1003397. PMID: 23555303.

Bozhenok et al. 2002. EMBO J. 21(9):2231-41. PMID: 11980720.


Add a reference

References: 2 entries

Sarshad et al. 2013. PLoS Genet. 9(3):e1003397. PMID: 23555303.

Bozhenok et al. 2002. EMBO J. 21(9):2231-41. PMID: 11980720.


Add a reference

References: 2 entries

Sarshad et al. 2013. PLoS Genet. 9(3):e1003397. PMID: 23555303.

Bozhenok et al. 2002. EMBO J. 21(9):2231-41. PMID: 11980720.


Add a reference


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