Overlay histogram showing Jurkat cells stained with ab109212 (red line). The cells were fixed with 80% methanol (5 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 (ab109212, 1/1000 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) (0.1μg/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 Jurkat cells fixed with 4% paraformaldehyde (10 min)/permeabilized with 0.1% PBS-Tween for 20 min used under the same conditions.
Western blot - ETS1 antibody [EPR546(2)] (ab109212)
All lanes : Anti-ETS1 antibody [EPR546(2)] (ab109212) at 1/1000 dilution
Lane 1 : MCF-7 cell lysate Lane 2 : Daudi cell lysate Lane 3 : Molt-4 cell lysate Lane 4 : PBMC lysate Lane 5 : HepG2 cell lysate Lane 6 : Jurkat cell lysate Lane 7 : Saos-2 cell lysate
Lysates/proteins at 10 µg per lane.
Predicted band size : 50 kDa
References for Anti-ETS1 antibody [EPR546(2)] (ab109212)
This product has been referenced in:
Luo W et al. A balance between B cell receptor and inhibitory receptor signaling controls plasma cell differentiation by maintaining optimal Ets1 levels. J Immunol193:909-20 (2014).
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