Anti-Type I arginase antibody produced in rabbit

Anti-Type I arginase antibody produced in rabbit Struktur
CAS-Nr.
Englisch Name:
Anti-Type I arginase antibody produced in rabbit
Synonyma:
Anti-Arginase-1;AntiArginase, liver;Anti-Type I arginase;AntiOTTHUMP00000017209;Anti-Liver-type arginase;Anti-ARG1 antibody produced in rabbit;Anti-Arginase-1 antibody produced in rabbit;Anti-ARG1 (AB1) antibody produced in rabbit;Anti-ARG1 (AB2) antibody produced in rabbit;Monoclonal Anti-ARG1 antibody produced in mouse
CBNumber:
CB22878270
Summenformel:
Molgewicht:
0
MOL-Datei:
Mol file

Anti-Type I arginase antibody produced in rabbit Eigenschaften

storage temp. 
-20°C
Aggregatzustand
buffered aqueous glycerol solution

Sicherheit

Anti-Type I arginase antibody produced in rabbit Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Western Blotting (1 paper)

Allgemeine Beschreibung

ARG1 (arginase 1) is an enzyme responsible for the processing of the essential amino acid arginine, to produce urea and L-ornithine. This enzyme is expressed in the presence of Th2 (T-helper) cytokines such as, interleukin (IL-4), IL-13 and TGFβ (tumor growth factor).

Biochem/physiol Actions

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 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.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

Anti-Type I arginase antibody produced in rabbit Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Anti-Type I arginase antibody produced in rabbit Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 14)Lieferanten
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  • Anti-ARG1 antibody produced in rabbit
  • Anti-Arginase-1 antibody produced in rabbit
  • Anti-Liver-type arginase antibody produced in rabbit
  • Anti-Type I arginase antibody produced in rabbit
  • Anti-Arginase-1
  • Anti-Liver-type arginase
  • Anti-Type I arginase
  • AntiArginase, liver
  • AntiOTTHUMP00000017209
  • Monoclonal Anti-ARG1 antibody produced in mouse
  • Anti-ARG1 (AB1) antibody produced in rabbit
  • Anti-ARG1 (AB2) antibody produced in rabbit
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