Immunofluorescence staining of Jurkat cells using anti-TAG-72 antibody Minretumomab (CC49) Immunofluorescence analysis of paraformaldehyde fixed Jurkat cells immobilized on Shi-fix cover-slips and stained with the chimeric rabbit IgG version of Minretumomab (CC49) at 10ug/ml followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing strong membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom, DAPI, merged channels and an isotype control. The isotype control was stained with anti-Fluorescein antibody followed by Alexa Fluor 488 secondary antibody.
Flow-cytometry using the anti-TAG-72 antibody Minretumomab (CC49). Jurkat cells were stained with anti-Fluorescein IgG antibody (4-4-20; isotype control, black line) or the rabbit IgG1 version of Minretumomab (CC49) (blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.
Immunofluorescence staining of Jurkat cells using anti-TAG-72 Minretumomab (CC49) Immunofluorescence analysis of paraformaldehyde fixed Jurkat cells stained with the chimeric mouse IgG version of Minretumomab (CC49) at 10ug/ml followed by Alexa Fluor 488 secondary antibody (2ug/ml), showing membrane staining. The nuclear stain is DAPI (blue). Panels show from left-right, top-bottom, DAPI, merged channels and an isotype control. The isotype control was stained with anti-unknown antibody followed by Alexa Fluor 488 secondary antibody.
Flow-cytometry using the anti-TAG-72 antibody Minretumomab (CC49). Jurkat cells were stained with anti-unknown IgG antibody or the mouse IgG-chimeric version of Minretumomab (CC49) (blue line) at a dilution of 1:100 for 1h at RT. After washing, bound antibody was detected using a goat anti-mouse IgG AlexaFluor 488 antibody at a dilution of 1:1000 and cells analyzed using a FACSCanto flow-cytometer.