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ProductsBack/Arginase 1 antibody [MSVA-511R] HistoMAX(tm)
IHC-P analysis of human liver tissue using GTX04426 Arginase 1 antibody [MSVA-511R] HistoMAX?. Strong nuclear and cytoplasmic arginase 1 expression in all hepatocytes in a normal liver.
IHC-P analysis of human liver tissue using GTX04426 Arginase 1 antibody [MSVA-511R] HistoMAX?. Strong nuclear and cytoplasmic arginase 1 expression in all hepatocytes in a normal liver.
IHC-P analysis of human liver tissue using GTX04426 Arginase 1 antibody [MSVA-511R] HistoMAX?. Strong nuclear and cytoplasmic arginase 1 expression in all hepatocytes in a normal liver.

Arginase 1 antibody [MSVA-511R] HistoMAX(tm)

GTX04426
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetARG1
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Overview

  • Supplier
    GeneTex
  • Product Name
    Arginase 1 antibody [MSVA-511R] HistoMAX(tm)
  • Delivery Days Customer
    9
  • Application Supplier Note
    IHC-P: 1:100-1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    MSVA-511R
  • Concentration
    0.2 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID383
  • Target name
    ARG1
  • Target description
    arginase 1
  • Target synonyms
    arginase-1, arginase, liver, liver-type arginase, type I arginase
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP05089
  • Protein Name
    Arginase-1
  • Scientific Description
    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. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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Figure 1. Western blot analysis of ARG1 using anti-ARG1 antibody (A01106). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HCCP tissue lysates, Lane 2: monkey liver tissue lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse liver tissue lysates, Lane 5: rat testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARG1 antigen affinity purified polyclonal antibody (Catalog # A01106) at 0.5 microg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARG1 at approximately 37 kDa. The expected band size for ARG1 is at 35 kDa.
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