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
Various whole cell lysates were separated by 4-20% SDS-PAGE, and the membrane was blotted with anti-Ctip2 antibody. The HRP-conjugated Goat anti-Rabbit IgG (H + L) antibody was used to detect the antibody.
IHC
Human tonsil was stained with anti-Ctip2 rabbit antibody.
IHC
Mouse spleen was stained with anti-Ctip2 rabbit antibody.
IHC
Rat spleen was stained with anti-Ctip2 rabbit antibody.
ICC/IF
Mouse spleen was stained with anti-Ctip2 rabbit antibody.
ICC/IF
Rat spleen was stained with anti-Ctip2 rabbit antibody.
ICC/IF
Immunofluorescence analysis of A431 cell. 1,primary Antibody was diluted at 1:200 (4℃ overnight). 2, Goat Anti Rabbit IgG (H&L) - AFluor 594 Secondary antibody was diluted at 1:500 (room temperature, 50min).