
Overlay histogram showing HeLa cells stained with ab124994 (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 (ab124994, 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) (0.1μg/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.
![All lanes : Anti-EEF1G antibody [EPR7200] (ab124994) at 1/10000 dilutionLane 1 : 293T cell lysateLane 2 : HL60 cell lysateLane 3 : C6 cell lysateLane 4 : RAW 264.7 cell lysateLane 5 : PC12 cell lysateLane 6 : NIH 3T3 cell lysateLane 7 : HepG2 cell lysateLane 8 : HeLa cell lysateLysates/proteins at 10 µg per lane.SecondaryGoat anti-Rabbit HRP at 1/2000 dilution](http://www.bioprodhub.com/system/product_images/ab_products/2/sub_2/11849_EEF1G-Primary-antibodies-ab124994-1.JPG)
All lanes : Anti-EEF1G antibody [EPR7200] (ab124994) at 1/10000 dilutionLane 1 : 293T cell lysateLane 2 : HL60 cell lysateLane 3 : C6 cell lysateLane 4 : RAW 264.7 cell lysateLane 5 : PC12 cell lysateLane 6 : NIH 3T3 cell lysateLane 7 : HepG2 cell lysateLane 8 : HeLa cell lysateLysates/proteins at 10 µg per lane.SecondaryGoat anti-Rabbit HRP at 1/2000 dilution

ab124994 at 1/250 dilution staining EEF1G in paraffin-embedded Human pancreatic adenocarcinoma tissue by Immunohistochemistry.

ab124994 at 1/100 dilution staining EEF1G in HeLa cells by Immunofluorescence.

Equilibrium disassociation constant (KD)Learn more about KD Click here to learn more about KD