WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the primary antibody was used at 4℃ over night with a 1:5000 dilution . The Dylight 800-conjugated Goat anti-Rabbit antibody was used to detect the antibody.
WB
Western blot analysis of lysates from 1) mouse-brain , 2) mouse-lung, 3) Hela cells, (Green) primary antibody was diluted at 1:1000, 4℃ over night, secondary antibody was diluted at 1:10000, 37° 1hour. (Red) GAPDH Monoclonal Antibody antibody was diluted at 1:5000 as loading control, 4℃ over night,secondary antibody was diluted at 1:10000, 37° 1hour.
WB
Western blot analysis of lysates from Jurkat WT and knockdown cell. Cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with Beclin 1 Rabbit mAb. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.
IHC
Rat kidney was stained with anti-Beclin 1 rabbit antibody.
IHC
Mouse kidney was stained with anti-Beclin 1 rabbit antibody.