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WBSCR17 Products

WBSCR17 encodes an N-acetylgalactosaminyltransferase, which has 97% sequence identity to the mouse protein. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq]
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5 results for "WBSCR17" in Products

5 results for "WBSCR17" in Products

WBSCR17 Products

WBSCR17 encodes an N-acetylgalactosaminyltransferase, which has 97% sequence identity to the mouse protein. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq]
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Applications: IHC, WB
Reactivity: Human, Mouse, Rat
Applications: IHC, WB
Reactivity: Human
Applications: WB, ELISA, MA, AP
Applications: WB
Applications: AC
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