Liver Arginase antibody

Catalog No. ABIN7464600

This Mouse Monoclonal antibody specifically detects Liver Arginase in WB, ELISA, FACS and IHC (p). It exhibits reactivity toward Human.

Quick Overview for Liver Arginase antibody (ABIN7464600)

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

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This Liver Arginase antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: GT5811

Product Details anti-Liver Arginase Antibody

Specificity: This antibody is specific for human Arginase 1 protein, and it does not cross react with human Arginase 2 protein.

Cross-Reactivity: Human, Mouse, Rat

Purification: Affinity purified by Protein A.

Immunogen: Full length human Arginase 1 recombinant protein.

Isotype: IgG2a

Application Details

Application Notes: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. FACS: 1:50-1:200. ELISA: 1:1000-1:10000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: Huh-7 , ARG1-transfected 293T

Validation: Overexpression

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 3.26 mg/mL

Buffer: PBS, No Preservative

Preservative: Without preservative

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for Liver Arginase

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

Alternative Name: arginase 1

Background: Arginase 1,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]

Molecular Weight: 35 kDa

Gene ID: 383

UniProt: P05089

Pathways: Cellular Response to Molecule of Bacterial Origin