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. 1998 Feb;36(2):531–538. doi: 10.1128/jcm.36.2.531-538.1998

FIG. 3.

FIG. 3

Levels of HBsAg, HBeAg, and intracellular replicative HBV DNA produced by HBV genomes amplified with Taq polymerase (A) or Taq-Pwo polymerase mixture (B). HBsAg and HBeAg were measured in the cell culture supernatant by enzyme immunoassays (Abbott), and the HBV DNA signals shown in Fig. 2 were quantified with TINA software (Raytest). The designation of the clones is the same as in Fig. 2. The values are given relative to that of the nonamplified wild-type genome (WT; open bar). Genomes which replicate at about wild-type genome level (range, WT/1.5 to WT × 1.5) are grouped (shaded bars), and those which were partially or completely sequenced are marked with an asterisk. Solid bars represent defective genomes.