WBSCR22 Products
WBSCR22 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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1 result for "WBSCR22" in Products
1 result for "WBSCR22" in Products
WBSCR22 Products
WBSCR22 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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Applications: WB, ELISA, ICC/IF, IP
Reactivity:
Human
| Reactivity: | Human |
| Details: | Mouse IgG2a Kappa Monoclonal Clone #2E12 |
| Applications: | WB, ELISA, ICC/IF, IP |
![Immunocytochemistry/ Immunofluorescence: WBSCR22 Antibody (2E12) [H00114049-M11]](https://resources.bio-techne.com/images/products/WBSCR22-Antibody-2E12-Immunocytochemistry-Immunofluorescence-H00114049-M11-img0001.jpg "Immunocytochemistry/ Immunofluorescence: WBSCR22 Antibody (2E12) [H00114049-M11]")