WBSCR17 Proteine
(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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WBSCR17
Spezies: Human
Wirt: Wheat germ
Recombinant
ELISA, WB, AA, AP
1 image
custom-made
WBSCR17
Spezies: Maus
Wirt: 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
Spezies: Human
Wirt: 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
Spezies: Maus
Wirt: 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
Spezies: Human
Wirt: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
ELISA, WB, SDS
WBSCR17
Spezies: Human
Wirt: Human Cells
Recombinant
Greater than 95 % as determined by reducing SDS-PAGE.
ELISA, WB, SDS, MS
Aliase für WBSCR17 Proteine
polypeptide N-acetylgalactosaminyltransferase 17 (GALNT17) ProteineWilliams-Beuren syndrome chromosome region 17 homolog (human) (Wbscr17) Proteine
AA388321 Proteine
E330012B09Rik Proteine
GALNACT17 Proteine
GALNT16 Proteine
GALNT20 Proteine
GALNTL3 Proteine
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