Anti-ARG1 Antibody, EPR6672(B)

Also for ARG1 (NM_000045)

Gene Name	Homo sapiens arginase, liver (ARG1), transcript variant 2
Synonyms:	OTTHUMP00000017209; arginase 1; liver-type arginase; type I arginase; arginase, liver
Immunogen	A synthetic peptide corresponding to residues in human ARG1 was used as an immunogen.
Buffer	Store at -20 °C. Buffer: Antibody buffer, sodium azide, glycerol, and BSA. Stable for 12 months from date of receipt.
Clone Name	EPR6672(B)	Isotype
Species Reactivity	Human	Concentration
Purification	(Protein A or G Sepharose)
Guaranteed Application *	WB, IHC	Suggested Dilutions	WB: 1:1,000 - 10,000; IHC 1:100 - 250; ICC: 1:100 - 250; FC: 1:10 - 100;
Background	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 ARG1 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 (1).
Related Pathway

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WB Image

Western blot analysis on (A) fetal liver and (B) fetal lung lysates using anti-ARG1 RabMAb.

IHC Image

Immunohistochemical analysis of paraffin-embedded human hepatocellular carcinoma tissue using anti-ARG1 RabMAb.

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Anti-ARG1 Antibody EPR6672(B)

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