alpha-L-Iduronidase/IDUA: Products

alpha-L-Iduronidase, encoded by the IDUA gene, is an important enzyme required for the lysosomal degradation of glycosaminoglycans (GAGs). It hydrolyzes the non-reducing terminal a-L-iduronic acid residues in GAGs, including dermatan sulfate and heparan sulfate. Mutations in IDUA that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I). MPS I causes progressive cellular, tissue, and organ damage.

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Recombinant Human alpha-L-Iduronidase/IDUA Protein, CF

 4119-GH 
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Human alpha -L-Iduronidase/IDUA Antibody

ICC/IF, IP, WBAF4119 
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Human alpha -L-Iduronidase/IDUA Antibody

WBMAB4119 
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Human alpha -L-Iduronidase/IDUA Biotinylated Antibody

WBBAF4119 
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