ab74793 staining PCBP1 in Human breast Tissue by Immunohistochemistry (Paraffin-embedded sections). Primary antibody used at 5 μg/ml
ab74793 staining PCBP1 in Human spleen Tissue by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) after heat treatment antigen retrieval. Primary antibody used at 5 μg/ml
Anti-PCBP1 antibody (ab74793) at 1 µg/ml (in 5% skim milk / PBS buffer) + HepG2 cell lysate at 10 µgSecondaryHRP conjugated anti-Rabbit IgG at 1/50000 dilution
ICC/IF image of ab74793 stained HeLa cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab74793, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
ab74793 at 5µg/ml staining PCBP1 in Human spleen tissue by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded tissue).
All lanes : Anti-PCBP1 antibody (ab74793) at 1 µg/mlLane 1 : Whole cell lysate prepared from MEF cellsLane 2 : Whole cell lysate prepared from F9 cellsLane 3 : Whole cell lysate prepared from GC1 cellsLane 4 : Whole cell lysate prepared from NIH-3T3 cellsLysates/proteins at 30 µg per lane.SecondaryHRP conjugated pig anti-rabbit polyclonaldeveloped using the ECL technique