Liver Arginase antibody (AA 293-322)

Catalog No. ABIN3030017

The Rabbit Polyclonal anti-Liver Arginase antibody has been validated for WB, ELISA, IHC and FACS. It is suitable to detect Liver Arginase in samples from Human.

Quick Overview for Liver Arginase antibody (AA 293-322) (ABIN3030017)

Target: Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Liver Arginase antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS)

Product Details anti-Liver Arginase Antibody

Binding Specificity: AA 293-322

Purification: Antigen affinity purified

Immunogen: A portion of amino acids 293-322 from the human protein was used as the immunogen for this ARG1 antibody.

Isotype: Ig Fraction

Application Details

Application Notes: Titration of the ARG1 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000,IHC (Paraffin): 1:50-1:100,Flow Cytometry: 1:10-1:50

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Aliquot the ARG1 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.

Target Details for Liver Arginase

Target: Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Alternative Name: ARG1

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 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.

UniProt: P05089

Pathways: Cellular Response to Molecule of Bacterial Origin