WBSCR22, CT (WBSCR22, Uncharacterized methyltransferase WBSCR22, Williams-Beuren syndrome chromosomal region 22 protein)

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.\n\nApplications:\nSuitable for use in Western Blot, ELISA\n\nRecommended Dilution:\nELISA: 1:1,000\nWestern Blot: 1:100-500\n\nStorage and Stability:\nMay be stored at 4 degrees C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degrees C. Aliquots are stable for 12 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

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SPECIFICATIONS

Catalog Number

043811

Size

200ul

Applications

ELISA, WB

Hosts

Rabbit

Reactivities

Hum

Form

Supplied as a liquid in PBS, pH 7.2, 0.09% sodium azide.

P Type

Pab

Purity

Purified by Protein A affinity chromatography.

Isotype

IgG

References

Lamesch, P., et al. Genomics 89(3):307-315(2007)\nAndersen, J.S., et al. Nature 433(7021):77-83(2005)\nWan, D., et al. Proc. Natl. Acad. Sci. U.S.A. 101(44):15724-15729(2004)\nMerla, G., et al. Hum. Genet. 110(5):429-438(2002)\nStanchi, F., et al. Yeast 18(1):69-80(2001)

Additional Info

Human

Alternative Names

WBSCR22, Uncharacterized methyltransferase WBSCR22, Williams-Beuren syndrome chromosomal region 22 protein