WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the primary antibody was used at 4℃ over night with a 1:2500 dilution . The Dilight 800-conjugated Goat anti-Rabbit antibody was used to detect the antibody.
WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-Bad antibody. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.
WB
Western Blot analysis of various cells using Cleaved-Bad (D71) Antibody
IHC
Rat kidney was stained with anti-Bad rabbit antibody.
IHC
Human kidney was stained with anti-Bad rabbit antibody.
IHC
Mouse kidney was stained with anti-Bad rabbit antibody.
IF-P
Mouse kidney was stained with anti-Bad rabbit antibody.
ICC/IF
Immunofluorescence analysis of HEK293. Picture A: Bad antibody (red). Picture B: DAPI (blue). Picture C: Merge of A+B.
ICC/IF
Immunofluorescence analysis of mouse-liver tissue. 1,Bad Antibody (red) was diluted at 1:200 (4℃ overnight). 2, Cy3 labled Secondary antibody was diluted at 1:300 (room temperature, 50min).3, Picture B: DAPI (blue) 10min. Picture A:Target. Picture B: DAPI. Picture C: merge of A+B.