WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the
membrane was blotted with anti-CD86 antibody. The HRP-
conjugated Goat anti-Rabbit IgG(H + L) antibody was used to detect the
antibody. Lane 1: J774A.1 Predicted band size: 35kDa Observed band size:60-85kDa
IHC
Mouse liver tissue was stained with Anti-CD86 rabbit Antibody
IHC
Mouse spleen was stained with anti-CD86 rabbit antibody
IF
Immunofluorescence analysis of paraffin-embedded Mouse spleen. Primary
Antibody was diluted at 1:200(4° overnight). an Multi colour-Fluorescence kit . EDTA based antigen retrieval was used before Green tyramide signal amplification. DAPI (dark blue) was used as a nuclear counter stain. Microscopy and pseudocoloring of individual dyes was performed using a Slideviewer Imaging System (3D histech).