GTX105840
WBSCR22 antibody
Cannot supply to this region.
- SKU:
- GTX105840
- Additional Names:
- BUD23 rRNA methyltransferase and ribosome maturation factor , HASJ4442 , HUSSY-3 , MERM1 , PP3381 , WBMT , WBSCR22
- Application:
- WB, IHC-P, IF, ICC, IP
- Concentration:
- 0.42 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human, Mouse
- Buffer:
- 0.1M Tris, 0.1M Glycine, 10% Glycerol; 1% BSA, 0.01% Thimerosal.
- Immunogen:
- Recombinant protein encompassing a sequence within the center region of human WBSCR22. The exact sequence is proprietary.
- Uniprot:
- O43709
- Synonyms:
- bud site selection protein 23 homolog;HASJ4442;HUSSY-3;MERM1;metastasis-related methyltransferase 1;PP3381;probable 18S rRNA (guanine-N(7))-methyltransferase;ribosome biogenesis methyltransferase WBSCR22;rRNA methyltransferase and ribosome maturation factor;WBMT;WBSCR22;Williams-Beuren candidate region putative methyltransferase;Williams-Beuren syndrome chromosomal region 22 protein;Williams-Beuren syndrome chromosome region 22
- Extra Details:
- 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]
- Shipping Conditions:
- Blue Ice