WBSCR22 antibody

GeneTex

WBSCR22 antibody

9

WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. IP: 1:500-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.

ImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin

Research Use Only

Polyclonal

0.42 mg/ml

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. [provided by RefSeq]

Human, Mouse

-20°C or -80°C,2°C to 8°C

12352203