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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7 results for "WBSCR22" in Products
7 results 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: IHC, WB, ICC/IF, IP
Reactivity:
Human,
Mouse
| Reactivity: | Human, Mouse |
| Details: | Rabbit IgG Polyclonal |
| Applications: | IHC, WB, ICC/IF, IP |
Applications: WB, ELISA, ICC/IF, IP
Reactivity:
Human
| Reactivity: | Human |
| Details: | Mouse IgG2a Kappa Monoclonal Clone #2E12 |
| Applications: | WB, ELISA, ICC/IF, IP |
Applications: WB
Reactivity:
Human,
Mouse,
Rat
| Reactivity: | Human, Mouse, Rat |
| Details: | Rabbit IgG Polyclonal |
| Applications: | WB |
Applications: IHC, ICC/IF
Reactivity:
Human
| Reactivity: | Human |
| Details: | Rabbit IgG Polyclonal |
| Applications: | IHC, ICC/IF |
| Reactivity: | Human |
| Details: | Mouse IgG Polyclonal |
| Applications: | WB, ICC/IF |
| Applications: | WB |
| Applications: | AC |