Liver Arginase anticorps (AA 293-322)

N° du produit ABIN3030017

L’anticorps Lapin Polyclonal anti-Liver Arginase a été validé pour WB, ELISA, IHC et FACS. Il convient pour détecter Liver Arginase dans des échantillons de Humain.

Aperçu rapide pour Liver Arginase anticorps (AA 293-322) (ABIN3030017)

Antigène: Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Liver Arginase est non-conjugé

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

Détail du produit anti-Liver Arginase anticorps

Épitope: AA 293-322

Purification: Antigen affinity purified

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

Isotype: Ig Fraction

Information d'application

Indications d'application: 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

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

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

Détails sur Liver Arginase

Antigène: Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Autre désignation: ARG1

Sujet: 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