ARG1

gene product
Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
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1026 antibodies from 41 providers.

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AntibodyRefsTypeWBELICCIPIHCFC
GeneTex
15 antibodies
Novus Biologicals
138 antibodies
Atlas Antibodies
3 antibodies
antibodies-online
329 antibodies
NovoPro Bioscience Inc.
8 antibodies
Proteintech Group
2 antibodies
R&D Systems
16 antibodies
St John's Laboratory
7 antibodies
Invitrogen Antibodies
12 antibodies
Biorbyt
58 antibodies
OriGene
17 antibodies
NSJ Bioreagents
11 antibodies
Aviva Systems Biology
9 antibodies
Boster Biological Technology
4 antibodies
Abgent
5 antibodies
Cell Signaling Technology, Inc
5 antibodies
Santa Cruz Biotechnology
1 antibody
LifeSpan BioSciences, Inc.
190 antibodies