WB
Western blot analysis of extracts from 293, using 5-HT-1A Antibody. The lane on the left was treated with blocking peptide.
WB
Western blot analysis of extracts from various samples, using 5HT1A Receptor Antibody. Lane 1: Hepg2 cells(serum starvation treatment), blocked with antigen-specific peptides. Lane 2: Hepg2 cells(serum starvation treatment). Lane 3: Hela cells(heat-shock treatment).
IHC
5HT1A Receptor Antibody at 1/100 staining Mouse spleen tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the primary antibody at 4°C overnight. An HRP conjugated anti-Rabbit antibody was used as the secondary antibody.
ICC/IF
5HT1A Receptor Antibody staining HepG2 by IF/ICC. The samples were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25°C. Samples were then incubated with primary Ab(1:200) and mouse anti-beta tubulin Ab(1:200) for 1 hour at 37°C. An AlexaFluor594 conjugated goat anti-rabbit IgG(H+L) Ab(Red) and an AlexaFluor488 conjugated goat anti-mouse IgG(H+L) Ab(Green) were used as the secondary antibody. The nuclear counter stain is DAPI(blue).