Williams-Beuren syndrome chromosomal region 16 protein, RCC1-like G exchanging factor-like protein, WBSCR16
Product description
This gene encodes an RCC1-like G-exchanging factor. It is
deleted in Williams syndrome, a multisystem developmental disorder
caused by the deletion of contiguous genes at 7q11.23. [provided by
RefSeq].1) Merla, G., et al. Hum. Genet. 110(5):429-438(2002)
Immunogen
This WBS16 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 15-44 amino acids from the N-terminal region of human WBS16.
Western blot analysis in CHO cell line lysates (35ug/lane).
Application Notes
For WB starting dilution is: 1:1000:
Additional Information
Form
Liquid
Storage Instructions
Store at 4˚C for three months and -20˚C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.