SGSH 蛋白
(N-Sulfoglucosamine Sulfohydrolase (SGSH))
This gene encodes one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with Sanfilippo syndrome A, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined. [provided by RefSeq, Jul 2008].
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8 results
SGSH
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
> 90 %
WB, SDS, Imm, PC
SGSH
宿主: 人
宿主: 人细胞
Recombinant
> 95 % as determined by reducing SDS-PAGE.
SGSH
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for SGSH 蛋白
N-sulfoglucosamine sulfohydrolase (SGSH) 蛋白N-sulfoglucosamine sulfohydrolase (Sgsh) 蛋白
N-sulfoglucosamine sulfohydrolase (sulfamidase) (Sgsh) 蛋白
4632406A19Rik 蛋白
HSS 蛋白
MPS3A 蛋白
SFMD 蛋白
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