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Liver Arginase Protein (active Mutant)

Dieses Recombinant Liver Arginase-Protein wird in Escherichia coli (E. coli) exprimiert.
Produktnummer ABIN6253489

Kurzübersicht für Liver Arginase Protein (active Mutant) (ABIN6253489)

Target

Alle Liver Arginase (ARG1) Proteine anzeigen
Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Protein-Typ

Recombinant

Spezies

  • 15
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Quelle

  • 9
  • 6
  • 5
  • 2
  • 1
  • 1
Escherichia coli (E. coli)

Reinheit

>90 % (SDS-PAGE)
  • Proteineigenschaft

    active Mutant

    Verwendungszweck

    Arginase I (human) (rec.) (highly active)

    Spezifität

    Full length human arginase I.

    Kreuzreaktivität

    Human

    Produktmerkmale

    Full length human arginase I.

    Biological Activity Comment

    1.6 ±0.2U/μg protein. One unit is defined as the amount of enzyme that converts 1μmol of L-arginine to L-ornithine and urea per min. at 37°C, pH 9.5 (according to protocol from R.T. Schimke, et al., J. Biol. Chem. 238, 1012 (1963)).
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    Expressionssystem
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  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.2 μg/μL

    Buffer

    In 10 mM TRIS-HCl, pH 7.5, containing 1 mM beta-mercaptoethanol, 1 mM MnCl2 and 50 % glycerol.

    Handhabung

    Avoid freeze/thaw cycles.

    Lagerung

    -20 °C,-80 °C

    Informationen zur Lagerung

    Short Term Storage: -20°C

    Long Term Storage: -80°C

    Use & Stability: Stable for at least 1 year after receipt when stored at -80°C.

    Haltbarkeit

    12 months
  • Target

    Liver Arginase (ARG1) (Arginase, Liver (ARG1))

    Andere Bezeichnung

    Arginase I

    Hintergrund

    EC 3.5.3.1, ARG1, Arginase 1, Type I Arginase, Liver-type Arginase, L-Arginase

    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 is involved in the nitric oxide (NO) pathway and immune cell arginine metabolism. It is fundamentally involved in cancer, inflammation, infections, fibrotic diseases, neurobiology, pregnancy and immune regulation in general.

    Molekulargewicht

    34.7kDa

    UniProt

    P05089

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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