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| Antigenic Specificity | WBSCR22 |
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| Clone | polyclonal |
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| Host Species | Rabbit |
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| Reactive Species | human |
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| Isotype | n/a |
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| Format | peptide affinity purified |
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| Size | 80 µl, 400 µl |
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| Concentration | n/a |
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| Applications | WB. RUO |
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| Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
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| Description | 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. This WBSCR22 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 253-281 amino acids from the C-terminal region of human WBSCR22. |
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| Immunogen | Human WBSCR22. |
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| Other Names | WBSCR22; Uncharacterized methyltransferase WBSCR22; Williams-Beuren syndrome chromosomal region 22 protein; Ribosome biogenesis methyltransferase WBSCR22; WBMT; MERM1; PP3381; HUSSY-3; HASJ4442 |
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| Gene, Accession # | WBSCR22, SwissProt: O43709 |
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| Catalog # | abx031474 |
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| Price | |
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| Order / More Info | WBSCR22 Antibody from ABBEXA |
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| Product Specific References | n/a |
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