WB
Western blot analysis of lysates from 1) HepG2, 2) K562,3) L929,4) MOUSE-BRAIN cells, (Green) primary antibody was diluted at 1:1000, 4°over night, secondary antibody was diluted at 1:10000, 37° 1hour. (Red) Actin β Monoclonal Antibody(5B7) antibody was diluted at 1:5000 as loading control, 4° over night,secondary antibody was diluted at 1:10000, 37° 1hour.
WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-CD31 antibody. The HRP-conjugated Goat anti-Rabbit IgG(H + L) antibody was used to detect the antibody. Lane 1: THP-1 Lane 2: Rat spleen.
IHC
Mouse lung was stained with anti-CD31 rabbit antibody.
IHC
Rat lung was stained with anti-CD31 rabbit antibody.
ICC/IF
Fluorescence multiplex immunohistochemical analysis of human tonsil tissue (formalin-fixed paraffin-embedded section). The immunostaining was performed by Sextuple-Fluorescence kit.CD3 rabbit mAb(RED), Ki67 rabbit mAb(GREEN), CD31 rabbit mAb(YELLOW), CD206 Rabbit mAb(WHITE) was tested with different TSA Fluorescence regent. Microscopy and pseudocoloring of individual dyes was performed using a Slideviewer Imaging System (Excilone).
ICC/IF
Immunofluorescence analysis of A549. 1,primary Antibody(red) was diluted at 1:200(4℃ overnight). 2, Goat Anti Rabbit IgG (H&L) - Alexa Fluor 594 Secondary antibody was diluted at 1:1000(room temperature, 50min).3, DAPI(blue) 10min.
ICC/IF
Mouse skin was stained with anti-CD31 Rabbit antibody.