Fig. 2.
Fig. 2. Southern blot hybridization of the duplicate RT-PCR results using an internal 5′-digoxigenine–labeled HCV probe. The initially detectable PCR products in duplicate of the 19 HCV seroconverters were blotted and hybridized under high-stringency conditions. The 19 seroconverters are indicated by an identification number. Positive and negative controls are indicated.

Southern blot hybridization of the duplicate RT-PCR results using an internal 5′-digoxigenine–labeled HCV probe. The initially detectable PCR products in duplicate of the 19 HCV seroconverters were blotted and hybridized under high-stringency conditions. The 19 seroconverters are indicated by an identification number. Positive and negative controls are indicated.

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