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Fig. 6

Fig. 6. Kinetics of incorporation into MHV RI/RF and subgenomic TI/TF RNA size classes. Infected cells were labelled at 6.5 h p.i. with [3H]uridine for 2–90 min periods, as indicated. Cell lysates were treated with RNase T1 to obtain the RF/TF cores, which were separated by electrophoresis on 1 % agarose gels. The area of the gels containing each RF/TF species (Open circle, RF; Filled circle, TF-II; Filled 
diamond, TF-III; Filled triangle, TF-IV; Filled 
inverted triangle, TF-V; Filled square, TF-VI; Open square, TF-VII) was cut out and its amount of radiolabelled RNA was determined by scintillation spectroscopy.

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