Hu, Mu, Rt, Bv, RbApplications:
WB, Simple Western, Flow, ICC/IF, IHC, IHC-Fr, IHC-P, IPHost:
Hu, Mu, RtApplications:
WB, Simple Western, Flow, ICC/IF, IHC, IHC-Fr, PEP-ELISAHost:
Hu, Mu, Rt, Po, Bv, Ca, Eq, Gt, GpApplications:
WB, IHC, IHC-PHost:
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 cross reactivity and physiologic function. The type I isoform, 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.
Bioinformatics Tool for Arginase 1/ARG1/liver Arginase
Discover related pathways, diseases and genes to Arginase 1/ARG1/liver Arginase. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.