Anti-mouse IgG (H+L) (DyLight™ 680 Conjugate)

In-Cell Western™ analysis of A549 cells exposed to varying concentrations of U0126 (MEK1/2 Inhibitor) #9903 for 3 hours, followed by TPA (Phorbol-12-Myristate-13-Acetate) #9905 stimulation for 30 minutes. With increasing concentrations of U0126, a significant decrease (~2.5 fold) in Phospho-p44/42 MAPK (Erk1/2) (Thr202/Tyr204) (E10) Mouse mAb #9106 signal as compared to the TPA-stimulated control was observed. Data and images were generated on the LI-COR® Biosciences Odyssey® Infrared Imaging System using Anti-mouse IgG (H+L) (DyLight® 680 Conjugate).In-Cell Western™分析暴露于不同浓度的U0126 (MEK1/2 抑制剂) #9903的A549细胞。暴露时间为3小时，然后用TPA（12-十四酸佛波酯-13-乙酸盐）刺激30分钟。 与TPA刺激的对照组相比较，随着刺激浓度的增加， Phospho-p44/42 MAPK (Erk1/2) (Thr202/Tyr204) (E10) Mouse mAb #9106的信号显著降低（约2.5倍）。数据和照片是在LI-COR ® Biosciences Odyssey ® Infrared 成像系统中生成的，所用抗体为Anti-mouse IgG (H+L) (DyLight ® 680 Conjugate)。

Western blot analysis of Jurkat cell lysates (#9194) treated with either U0126 (MEK 1/2 inhibitor) #9903 or TPA (12-O-Tetradecanoylphorbol-13-Acetate) #4174, using Phospho-p44/42 MAPK (Erk1/2) (Thr202/204) (D13.14.4E) XP® Rabbit mAb #4370 detected with Anti-rabbit IgG (H+L) (DyLight® 800 Conjugate) #5151 (green) and p44/42 MAPK (Erk1/2) (3A7) Mouse mAb #9107 detected with Anti-mouse IgG (H+L) (DyLight® 680 Conjugate) (red). The array image pixel intensities obtained using a LI-COR® Biosciences Odyssey® Infrared Imaging System are shown in the top figure while corresponding fluorescent western blots are shown in the bottom figure.Western blot分析U0126 (MEK 1/2 inhibitor) #9903 或 TPA (12-十四酸佛波酯-13-乙酸盐) #4174处理的Jurkat细胞(#9194)提取物。所用抗体有Phospho-p44/42 MAPK (Erk1/2) (Thr202/204) (D13.14.4E) XP™ Rabbit mAb #4370 ，检测用Anti-rabbit IgG (H+L) (DyLight ® 800 Conjugate) #5151 (绿色)和p44/42 MAPK (Erk1/2) (3A7) Mouse mAb #9107 检测用Anti-mouse IgG (H+L) (DyLight ® 680 Conjugate) (红色)。上图一系列的像素强度是用LI-COR ® Biosciences Odyssey ® Infrared 成像系统中获得的；下图为相对应的荧光western blots结果。