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Liver Arginase Protein (active Mutant)

This Recombinant Liver Arginase protein is expressed in Escherichia coli (E. coli).
Catalog No. ABIN6253489

Quick Overview for Liver Arginase Protein (active Mutant) (ABIN6253489)

Target

See all Liver Arginase (ARG1) Proteins
Liver Arginase (ARG1) (Arginase, Liver (ARG1))

Protein Type

Recombinant

Origin

  • 14
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Source

  • 8
  • 6
  • 5
  • 2
  • 1
  • 1
Escherichia coli (E. coli)

Purity

>90 % (SDS-PAGE)
  • Protein Characteristics

    active Mutant

    Purpose

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

    Specificity

    Full length human arginase I.

    Cross-Reactivity

    Human

    Characteristics

    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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  • Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.2 μg/μL

    Buffer

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

    Handling Advice

    Avoid freeze/thaw cycles.

    Storage

    -20 °C,-80 °C

    Storage Comment

    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.

    Expiry Date

    12 months
  • Target

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

    Alternative Name

    Arginase I

    Background

    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.

    Molecular Weight

    34.7kDa

    UniProt

    P05089

    Pathways

    Cellular Response to Molecule of Bacterial Origin
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