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  Indian J Med Microbiol
 

Figure 4: Migration of HeLa cell observed under fluorescent cell imager using brightfield mode with 20X objective (ZOE™ fluorescent cell imager). Row A represents before (Aa) and after (Ab) applying of scratcher and generating 0.5 mm wound. After the scratch was applied, the monolayer cell lines were treated with media (control group, row B), 50 μM trolox (row C), 125 μg/ml Leucaena leucocephala (row D) and 125 μg/ml Dracaena serrulata (row E). The width of the wound was measured at 3 (Ba, Ca, Da, Ea), 6 (Bb, Cb, Db, Eb), 12 (Bc, Cc, Dc, Ec) and 24 h (Bd, Cd, Dd, Ed) using image J program

Figure 4: Migration of HeLa cell observed under fluorescent cell imager using brightfield mode with 20X objective (ZOE™ fluorescent cell imager). Row A represents before (Aa) and after (Ab) applying of scratcher and generating 0.5 mm wound. After the scratch was applied, the monolayer cell lines were treated with media (control group, row B), 50 μM trolox (row C), 125 μg/ml <i>Leucaena leucocephala</i> (row D) and 125 μg/ml <i>Dracaena serrulata</i> (row E). The width of the wound was measured at 3 (Ba, Ca, Da, Ea), 6 (Bb, Cb, Db, Eb), 12 (Bc, Cc, Dc, Ec) and 24 h (Bd, Cd, Dd, Ed) using image J program