WBSCR22 antibody

GeneTex

WBSCR22 antibody

9

WB: 1:500 - 1:2000. ICC/IF: 1:50 - 1:100. IHC-P: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.

ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin

Research Use Only

Polyclonal

Unconjugated

BUD23

BUD23 rRNA methyltransferase and ribosome maturation factor

HASJ4442, HUSSY-3, MERM1, PP3381, WBMT, WBSCR22, 18S rRNA (guanine-N(7))-methyltransferase, Williams-Beuren candidate region putative methyltransferase, Williams-Beuren syndrome chromosomal region 22 protein, Williams-Beuren syndrome chromosome region 22, bud site selection protein 23 homolog, metastasis-related methyltransferase 1, probable 18S rRNA (guanine-N(7))-methyltransferase, rRNA methyltransferase and ribosome maturation factor, ribosome biogenesis methyltransferase WBSCR22

Rabbit

IgG

18S rRNA (guanine-N(7))-methyltransferase

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. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011]

Human, Rat

-20°C or -80°C,2°C to 8°C

12352203