ContactosContactos
Using a secondary antibody fluorophore combination reversed from that in the section linked directly above (but the same primary cocktail), a second monolayer culture of HJ1.Ov cells was triple-labeled using double immunofluorescence and a phallotoxin. Nuclei were visualized with mouse anti-NPCP (nuclear pore complex protein) primary antibodies, while the Golgi complex was stained with rabbit anti-giantin antibodies. Secondary antibodies were goat anti-mouse and anti-rabbit conjugated to Alexa Fluor 568 and 488, respectively to produce red nuclei and green Golgi cisternae. The filamentous actin network was counterstained with Alexa Fluor 350 conjugated to phalloidin.
Not Available in Your Country
Sorry, this page is not available in your country.
You are being redirected to our local site.