| 产品详情 |
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| Product Name | Recombinant Human Uncharacterized methyltransferase WBSCR22 (WBSCR22) |
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| Description | 1-281aa, Full length protein. MW: 33,846 Da. Purity >85% (SDS-PAGE). 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. |
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| Size | 0.05 mg (E-Coli), 0.2 mg (E-Coli), 0.05 mg (Baculovirus), 0.5 mg (E-Coli), 0.2 mg (Yeast) |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | [probable 18S rRNA (guanine-N(7))-methyltransferase isoform 1; Probable 18S rRNA (guanine-N(7))-methyltransferase; probable 18S rRNA (guanine-N(7))-methyltransferase; BUD23, rRNA methyltransferase and ribosome maturation factor; Bud site selection protein 23 homolog; Metastasis-related methyltransferase 1; Williams-Beuren syndrome chromosomal region 22 protein; rRNA methyltransferase and ribosome maturation factor] |
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| Gene, Accession, CAS # | WBSCR22, Gene ID: 114049, Accession: NP_001189489.1 |
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| Catalog # | MBS1173127 |
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| Price | |
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| Order / More Info | Recombinant Human Uncharacterized methyltransferase WBSCR22 (WBSCR22) from MYBIOSOURCE INC. |
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| Product Specific References | n/a |
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