WB
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-FOXP3 antibody. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.
IHC
Mouse spleen was stained with Anti-FOXP3 rabbit antibody.
IHC
Rat spleen was stained with Anti-FOXP3 rabbit antibody.
IHC
Human tonsil was stained with Anti-FOXP3 rabbit antibody.
IF-P
mouse spleen was stained with Anti-FOXP3 rabbit antibody.
IF-P
Fluorescence multiplex immunohistochemical analysis of Human bladder tissue (formalin-fixed paraffin-embedded section).
The immunostaining was performed by Sextuple-Fluorescence kit. CD8 rabbit mAb cyan, FOXP3 rabbit mAb red,Neurofilament mouse mAb purple,Iba 1 mouse mAb red, CD20 mouse mAb yellow,
The section was incubated in 4 rounds of staining; sequentially for Anti-antibodies; each using a separate fluorescent tyramide signal amplification system. EDTA based antigen retrieval (pH 9.0, 20 minutes) was used in between rounds of tyramide signal amplification to remove the antibody from the previous round, to avoid any cross-reactivity. DAPI (dark blue) was used as a nuclear counter stain.
Microscopy and pseudocoloring of individual dyes was performed using a Slideviewer Imaging System (Excilone).