Liver Arginase anticorps

N° du produit ABIN7464600

Cet anticorps Souris Monoclonal détecte spécifiquement Liver Arginase dans WB, ELISA, FACS et IHC (p). Il présente une réactivité envers Humain.

Aperçu rapide pour Liver Arginase anticorps (ABIN7464600)

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

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Liver Arginase est non-conjugé

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

Clone: GT5811

Détail du produit anti-Liver Arginase anticorps

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

Réactivité croisée: Humain, Souris, Rat

Purification: Affinity purified by Protein A.

Immunogène: Full length human Arginase 1 recombinant protein.

Isotype: IgG2a

Information d'application

Indications d'application: 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.

Commentaires:

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

Validation: Overexpression

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 3.26 mg/mL

Buffer: PBS, No Preservative

Agent conservateur: Without preservative

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur Liver Arginase

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

Autre désignation: arginase 1

Sujet: 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]

Poids moléculaire: 35 kDa

ID gène: 383

UniProt: P05089

Pathways: Cellular Response to Molecule of Bacterial Origin