IDUA

gene product
MPS1, MPSI
This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I). [provided by RefSeq, Jul 2008]
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221 antibodies from 26 providers.

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Antibody
R&D Systems
3 antibodies
Novus Biologicals
5 antibodies
antibodies-online
73 antibodies
NovoPro Bioscience Inc.
2 antibodies
Abgent
2 antibodies
GeneTex
1 antibody
Invitrogen Antibodies
4 antibodies
Proteintech Group
1 antibody
Aviva Systems Biology
3 antibodies
LifeSpan BioSciences, Inc.
48 antibodies
Atlas Antibodies
2 antibodies
Cusabio Biotech Co., Ltd
5 antibodies
Abbkine Scientific Co.Ltd.
1 antibody
Boster Biological Technology
1 antibody
Wuhan Fine Biotech Co., Ltd.
1 antibody
Biorbyt
11 antibodies
OriGene
2 antibodies
MyBioSource
4 antibodies
Creative Diagnostics
3 antibodies
United States Biological
15 antibodies
Creative Biolabs
5 antibodies
St John's Laboratory
3 antibodies
Abbexa
9 antibodies
Leading Biology
1 antibody
MilliporeSigma / Merck KGaA
1 antibody