GAA

gene product
This gene encodes lysosomal alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. The encoded preproprotein is proteolytically processed to generate multiple intermediate forms and the mature form of the enzyme. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
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324 antibodies from 31 providers.

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Proteintech Group
1 antibody
GeneTex
2 antibodies
antibodies-online
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Novus Biologicals
6 antibodies
Boster Biological Technology
3 antibodies
Cusabio Biotech Co., Ltd
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NovoPro Bioscience Inc.
2 antibodies
Atlas Antibodies
2 antibodies
LifeSpan BioSciences, Inc.
96 antibodies
Biorbyt
15 antibodies
HUABIO Research
1 antibody
OriGene
3 antibodies
Aviva Systems Biology
2 antibodies
Acris Antibodies GmbH
2 antibodies
Abnova Corporation
5 antibodies
Abgent
1 antibody
NSJ Bioreagents
1 antibody
Invitrogen Antibodies
6 antibodies
RabMAbs
2 antibodies
MyBioSource
6 antibodies
ProSci
1 antibody
Creative Biolabs
12 antibodies
Abbexa
9 antibodies
St John's Laboratory
1 antibody
United States Biological
26 antibodies
MilliporeSigma / Merck KGaA
7 antibodies
EMD Millipore
1 antibody
Leading Biology
1 antibody
RayBiotech, Inc.
1 antibody
Creative Diagnostics
1 antibody