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Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)

Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
  • 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)
  • 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)

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Images

  • Western blot - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    Western blot - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    All lanes : Anti-JNK3 antibody [EPR5493(2)] (ab126591) at 1/1000 dilution

    Lane 1 : HeLa cell lysate
    Lane 2 : 293T cell lysate
    Lane 3 : SH-SY5Y cell lysate
    Lane 4 : Human heart tissue lysate

    Lysates/proteins at 10 µg per lane.

    Secondary
    All lanes : Goat anti-rabbit HRP conjugated at 1/2000 dilution

    Predicted band size: 53 kDa



    This data was developed using ab126591, the same antibody clone in a different buffer formulation.

  • Flow Cytometry - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    Flow Cytometry - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    This data was developed using ab126591, the same antibody clone in a different buffer formulation.Overlay histogram showing SHSY-5Y cells stained with ab126591 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab126591, 1/10000 dilution) for 30 min at 22°C. The secondary antibody used was Alexa Fluor® 488 goat anti-rabbit IgG (H&L) (ab150077) at 1/2000 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit IgG (monoclonal) (0.1?g/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 20mW Argon ion laser (488nm) and 525/30 bandpass filter. This antibody gave a positive signal in SHSY-5Y cells fixed with 80% methanol (5 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
  • Immunocytochemistry - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    Immunocytochemistry - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    This data was developed using ab126591, the same antibody clone in a different buffer formulation.ab126591 at 1/100 dilution staining JNK3 in 293 cells by immunofluorescence.
  • ELISA - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    ELISA - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)

    This data was developed using ab126591, the same antibody clone in a different buffer formulation.

    ELISA analysis of Human JNK3 recombinant protein at 1000 ng/mL with ab126591. An Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution was used as the secondary antibody.
  • OI-RD Scanning - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    OI-RD Scanning - Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    This data was developed using ab126591, the same antibody clone in a different buffer formulation.Equilibrium disassociation constant (KD)
    Learn more about KD

    Click here to learn more about KD
  • Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)
    Anti-JNK3 antibody [EPR5493(2)] - BSA and Azide free (ab248117)

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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