FIG. 2.

Regions of gM are sufficient to enable gN modification and transport. Cos7 cells were transfected with the indicated plasmids, and protein expression was assayed by reactivity with MAb 14-16A (anti-gM/gN) and MAb 9E10 (anti-Myc). Reactivity was detected with a fluorescein isothiocyanate-conjugated anti-mouse • •chain-specific antibody. MAb 9E10 was detected with a Texas Red-conjugated anti-mouse IgG1 second antibody. The appearance of yellow in the merged pictures indicates colocalization of signals.