Ab7797

Cells were cultured in four well TEK slides (Fisher) and fixed for 10 min using freshly made 4% neutral-buffered formalin. Primary rabbit monoclonal antibodies to keratin 14 (K14, ab51054, Abcam) and mouse monoclonal antibody to K18 (ab7797, Abcam) were used for double staining. Secondary donkey anti mouse antibody (ab150105, Abcam) with Alexa 488 tag and secondary goat anti rabbit antibody (ab150080, Abcam) with an Alexa 594 tag were used for visualization. Negative controls consisted of irrelevant primary antibodies including rabbit monoclonal isotype control (ab172730, Abcam) and mouse monoclonal isotype control (ab170190, Abcam). Primary mouse monoclonal antibody to K17 (ab188859, Abcam), mouse monoclonal antibody to MMP7 (sc-515703, Santa Cruz) and rabbit monoclonal antibodies to p63 (#13109S, Cell Signaling) were used for single staining. The dilution ratio for all primary antibodies was 1:300 and the dilution ratio for all secondary antibodies was 1:500. The gain and exposure time of the fluorescence microscope were adjusted to show positively stained cells while negative control cells had no staining. Staining percentage was calculated by dividing the positively stained cell number by the total cell number. Staining intensity was measured by ImageJ and the negative control was used to subtract background.

We fixed raft cultures in 4% neutral buffered formalin and then embedded in paraffin for sectioning and hematoxylin and eosin (H&E) staining. Primary rabbit monoclonal antibodies to keratin 14 (ab51054, Abcam) and Ki-67 (ab16667, Abcam) and primary mouse monoclonal antibodies to K18 (ab7797, Abcam), pAkt1 (sc-293125, Santa Cruz) and MMP-1 (sc-21731, Santa Cruz) were used for immunohistochemistry on unstained sections. Secondary donkey anti-mouse antibody (ab150105, Abcam) with Alexa 488 tag and secondary goat anti-rabbit antibody (ab150080, Abcam) with an Alexa 594 tag were used for visualization. Negative controls consisted of irrelevant primary antibodies including rabbit monoclonal isotype control (ab172730, Abcam) and mouse monoclonal isotype control (ab170190, Abcam). The gain and exposure time of the fluorescence microscope were adjusted to show positively stained cells while negative control cells had no staining. Staining percentage was calculated by dividing the positively stained cell number by the total cell number. Staining intensity was measured by ImageJ and the negative control was used to subtract background.