ab8741 staining Cytokeratin 16 in Human hyperproliferative skin lesion (ulcus)tissue sections by IHC-P (Formaldehyde-fixed, Paraffin-embedded sections). Tissue samples were fixed with formaldehyde and blocked with 10% Serum for 30 minutes at 21°C; antigen retrieval was by heat mediation in citrate buffer (pH 6). The sample was incubated with primary antibody (1/50 in PBS + 0.5% Tween-20 + 0.5% BSA) at 21°C for 30 minutes. An undiluted HRP-conjugated goat polyclonal to mouse IgG was used as secondary antibody.See Abreview
ICC/IF image of ab8741 stained HeLa cells. The cells were 100% methanol fixed (5 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 (ab8741, 5µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse 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.
ab8741 staining Cytokeratin 16 in sheep epithelial tissue by Immunohistochemistry (Frozen sections).Tissue was fixed in acetone, permeabilized using Tween 20, blocked with 10% serum for 2 hours at 20°C and then incubated with ab8741 at a 1/40 for 12 hours at 4°C. The secondary used was ab98640 Goat F(ab')2 polyclonal Secondary Antibody to Mouse IgG - H&L (DyLight® 650), used at a 1/500 dilution.See Abreview