*Optimal dilutions/concentrations should be determined by the researcher.
Not tested in other applications.
HeLa , HCT116 , *A375M ,
Bovine, Rhesus Monkey(>80% identity)
0.1M Tris, 0.1M Glycine, 10% Glycerol (pH7). 0.01% Thimerosal was added as a preservative.
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
0.42mg/ml(Please refer to the vial label for the specific concentration.)
Recombinant protein encompassing a sequence within the center region of human WBSCR22. The exact sequence is proprietary.
Purified by antigen-affinity chromatography.
For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
FLJ44236 antibody, HASJ4442 antibody, HUSSY-3 antibody, MGC19709 antibody, MGC2022 antibody, MGC5140 antibody, PP3381 antibody, WBMT antibody, WBSCR22 antibody, Williams-Beuren candidate region putative methyltransferase antibody, Williams-Beuren syndrome chromosomal region 22 protein antibody, uncharacterized methyltransferase WBSCR22 antibody, Williams Beuren syndrome chromosome region 22 antibody
This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq]