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Neuroscience Neurotransmission Nitric Oxide NOS

Anti-iNOS antibody (ab3523)

Anti-iNOS antibody (ab3523)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)
  • ChIP - Anti-Histone H3 antibody - Nuclear Loading Control and ChIP Grade (ab1791)

Key features and details

  • Rabbit polyclonal to iNOS
  • Suitable for: ICC/IF, IHC
  • Reacts with: Mouse, Human
  • Isotype: IgG

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Overview

  • Product name

    Anti-iNOS antibody
    See all iNOS primary antibodies
  • Description

    Rabbit polyclonal to iNOS
  • Host species

    Rabbit
  • Specificity

    This antibody detects iNOS. It does not detect other NOS isoforms. By western blot, this antibody detects an ~135 kDa protein representing recombinant human iNOS. By western blot, this antibody also detects purified recombinant mouse iNOS, mouse iNOS from cytokine stimulated RAW 264.7 cells.
  • Tested Applications & Species

    Application Species
    ICC/IF
    Mouse
    Human
    IHC
    Human
    See all applications and species data
  • Immunogen

    Synthetic peptide corresponding to Mouse iNOS aa 1-100.
    Database link: P29477

    Run BLAST with BLAST the sequence with ExPASy Run BLAST with BLAST the sequence with NCBI
  • Positive control

    • ICC: A549, NIH/3T3 cells. IHC-P: Human heart tissue.

Properties

  • Form

    Liquid
  • Storage instructions

    Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C long term. Avoid freeze / thaw cycle.
  • Storage buffer

    Preservative: 0.05% Sodium azide
    Constituents: 0.1% BSA, 99% PBS
  • Concentration information loading...
  • Purity

    Immunogen affinity purified
  • Clonality

    Polyclonal
  • Isotype

    IgG
  • Research areas

    • Neuroscience
    • Neurotransmission
    • Nitric Oxide
    • NOS
    • Cancer
    • Cancer Metabolism
    • Response to hypoxia
    • Cancer
    • Cancer Metabolism
    • Cellular metabolic process
    • Metabolism
    • Pathways and Processes
    • Metabolism processes
    • Hypoxia
    • Metabolism
    • Types of disease
    • Cancer

Images

  • Immunohistochemistry - Anti-iNOS antibody (ab3523)
    Immunohistochemistry - Anti-iNOS antibody (ab3523)

    Immunohistochemistry analysis of human heart tissue stained for iNOS without (negative control) or using ab3523 at 1/200 dilution overnight at 4°C in a humidified chamber, followed biotin-conjugated secondary antibody and SA-HRP, followed by colorimetric detection using DAB. Tissues were counterstained with hematoxylin and prepped for mounting. Tissues were washed extensively with PBST and endogenous peroxidase activity was quenched with a peroxidase suppressor.

    To expose target proteins, heat induced antigen retrieval was performed using 10mM sodium citrate (pH6.0) buffer, microwaved for 8-15 minutes. Following antigen retrieval tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature.

  • Immunocytochemistry/ Immunofluorescence - Anti-iNOS antibody (ab3523)
    Immunocytochemistry/ Immunofluorescence - Anti-iNOS antibody (ab3523)

    Immunofluorescence analysis of A549 (human lung carcinoma cell line) whole cells labelling iNOS (Left panel: green) without (control) or using ab3523 at 1/20 dilution overnight at 4°C, followed DyLight-488 conjugated secondary antibody. Counter stain: F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.

    Cells were grown on chamber slides and fixed with formaldehyde prior to staining.

     

  • Immunocytochemistry/ Immunofluorescence - Anti-iNOS antibody (ab3523)
    Immunocytochemistry/ Immunofluorescence - Anti-iNOS antibody (ab3523)

    Immunofluorescence analysis of NIH/3T3 (mouse embryo fibroblast cell line) whole cells labelling iNOS (Left panel: green) without (control) or using ab3523 at 1/20 dilution overnight at 4°C, followed DyLight-488 conjugated secondary antibody. Counter stain: F-Actin staining with Phalloidin (red) and nuclei with DAPI (blue) is shown. Images were taken at 60X magnification.

    Cells were grown on chamber slides and fixed with formaldehyde prior to staining.

     

Please note: All products are "FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES"
For licensing inquiries, please contact partnerships@abcam.com

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