WBSCR17 蛋白
(Williams-Beuren Syndrome Chromosome Region 17 (WBSCR17))
This gene encodes an N-acetylgalactosaminyltransferase. This gene is located centromeric to the common deleted region in Williams-Beuren syndrome (WBS), a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. This protein may play a role in membrane trafficking. [provided by RefSeq, Jan 2013].
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6 results
custom-made
WBSCR17
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
WBSCR17
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
WBSCR17
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
custom-made
WBSCR17
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
WBSCR17
宿主: 人
宿主: 人细胞
Recombinant
Greater than 95 % as determined by reducing SDS-PAGE.
ELISA, WB, SDS, MS
Aliases for WBSCR17 蛋白
polypeptide N-acetylgalactosaminyltransferase 17 (GALNT17) 蛋白Williams-Beuren syndrome chromosome region 17 homolog (human) (Wbscr17) 蛋白
AA388321 蛋白
E330012B09Rik 蛋白
GALNACT17 蛋白
GALNT16 蛋白
GALNT20 蛋白
GALNTL3 蛋白
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