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Arginase, Liver (ARG1) (N-Term) Peptide

ARG1 Reactivité: Humain Hôte: Synthetic BP, IHC, WB
N° du produit ABIN973376
  • Antigène Tous les produits Liver Arginase (ARG1)
    Liver Arginase (ARG1) (Arginase, Liver (ARG1))
    Protein Region
    N-Term
    Origine
    Humain
    Source
    • 12
    Synthetic
    Application
    Blocking Peptide (BP), Immunohistochemistry (IHC), Western Blotting (WB)
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-ARG1 antibody (Catalog #: ARP45671_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Indications d'application
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    Liver Arginase (ARG1) (Arginase, Liver (ARG1))
    Synonymes
    SI:zC146F4.4 (novel protein with NUDIX domain) Peptide, si:ch211-146f4.3 Peptide, argi1 Peptide, AI Peptide, AI256583 Peptide, Arg-1 Peptide, PGIF Peptide, arginase 1 Peptide, arginase Peptide, Arginase-1 Peptide, arginase, liver Peptide, L-arginase Peptide, arg1 Peptide, PGTG_16455 Peptide, argi1 Peptide, ARG1 Peptide, Arg1 Peptide
    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 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.

    Alias Symbols: -

    Protein Interaction Partner: ARG2,FLOT1,NOS1,USP53

    Protein Size: 322
    Poids moléculaire
    35 kDa
    ID gène
    383
    NCBI Accession
    NM_000045, NP_000036
    UniProt
    P05089
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