ARG1

ARG1

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. [provided by RefSeq].

 

Alternative names: ARG1; OTTHUMP00000017209; Arginase 1; liver-type arginase; type I arginase; arginase, liver.

Product Name: Anti-ARG1 Antibody
Reference #: CE00080
Clone #: 4E6
Source #: Mouse Monoclonal
Reactivity: Human
Catalog Number &
Aliquote Size #:
C0080MA01-MA | 0.1 mL
C0080MA05-MA | 0.5 mL
C0080MA10-MA | 1.0 mL

Click the buttons below to download the corresponding PDF.

Coming Soon.

Other Products You May Like

Element

Become a Member


Continue

By continuing to use this site you agree to the use of cookies

SDIX uses cookies to improve your experience on the website and to provide you with services and content tailored to your interests

Learn more about The SDIX Cookie Policy

Learn more about The SDIX Privacy Policy

You have Successfully Subscribed!