AGA

gene product
ASRG
Aspartylglucosaminidase is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Jan 2010]
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147 antibodies from 21 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
Bioworld Technology, Inc
1 antibody
GeneTex
1 antibody
LifeSpan BioSciences, Inc.
35 antibodies
Biorbyt
9 antibodies
NovoPro Bioscience Inc.
1 antibody
Atlas Antibodies
2 antibodies
antibodies-online
45 antibodies
OriGene
3 antibodies
Proteintech Group
1 antibody
Invitrogen Antibodies
4 antibodies
Novus Biologicals
3 antibodies
St John's Laboratory
2 antibodies
Abnova Corporation
4 antibodies
Acris Antibodies GmbH
1 antibody
Aviva Systems Biology
1 antibody
United States Biological
24 antibodies
MyBioSource
3 antibodies
Boster Biological Technology
1 antibody
Abbexa
3 antibodies
Creative Diagnostics
2 antibodies
Sigma-Aldrich
1 antibody