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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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9 results for "WBSCR22" in Products

9 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
Applications: WB, ELISA, ICC/IF, IP
Reactivity: Human
Applications: WB
Reactivity: Human, Mouse, Rat
Applications: WB, ICC/IF
Reactivity: Human
Applications: IHC, ICC/IF
Reactivity: Human
Catalog #: H00114049-Q01
Applications: WB, ELISA, MA, AP
Applications: WB, ELISA, MA, AP
Applications: WB
Applications: AC
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