<p>(A) DSL212 cells were cultured in the absence of tetracycline for 6 days. Cytoplasm and nuclei were fractionated with QIAgen Qproteome Cell Compartment Kit by following the manufacturer's directions. DHBV core-associated DNA and Hirt DNA were extracted from whole cell, cytoplasm and nuclear fractions were analyzed by Southern blot assay. (B) DHBV core-associated DNA and Hirt DNA were extracted from whole cell, cytoplasm and nuclear fractions of HepG3 cells (a HepG2-derived stable cell line containing an integrated DHBV head-to-tail unit-length DNA dimer) were analyzed by Southern blot assay.</p
<p>(A) and (B). HEK293 cells in 6 cm dishes were cotransfected with the envelope-defective HBV (5 μg...
<p>To examine HBV DNA synthesis in core particles with chimeric C variants, the C-deficient mutant a...
<p>1.3ES2 cells were treated with or without TGF-β1 for 6 days. (A) Total DNA was extracted followed...
<p>The indicated cell lines were seeded onto 6-well plate and infected with AdDHBV1S at a MOI of 10....
<p>HepG2 cells, with (241, lanes 2, 5, 8, 11, 14; 245, lanes 3, 6, 9, 12, 15) or without (WT, lanes ...
<p>DSL212 cells were seeded in 6-well plates and cultured in the presence of tetracycline (1 μg/ml) ...
<p>Cell lines used in this experiment are CHO-K1 and its derived cell line Xrs-5 harboring defective...
<p>Dstet5 cells were treated and harvested as depicted in the top panel. DHBV mRNA (A), cytoplasmic ...
<p>Cells were mock infected or infected with HBV at indicated inoculum size (vge/cell) in the presen...
<p>HEK293T cells were cotransfected with pCMV-DHBV/C-, which expresses a core-defective DHBV genome,...
<p>Dstet5 cells were treated and harvested as depicted in the top panel. DHBV mRNA (A), cytoplasmic ...
AbstractAll tissue culture systems for propagating HBV employed so far make use of tandemly arranged...
Related to Fig 4. HepAD38 (DOX-) cells were treated with Bay 41–4109 or GLS4. After 3 days, extracel...
(A) Isolated Smc5 and Smc6 proteins from whole cell lysate, cytoplasmic and nuclear fractions of Hep...
<p><b>(A) Selection of well-performing cell clones.</b> Clones preselected for the presence of HBV D...
<p>(A) and (B). HEK293 cells in 6 cm dishes were cotransfected with the envelope-defective HBV (5 μg...
<p>To examine HBV DNA synthesis in core particles with chimeric C variants, the C-deficient mutant a...
<p>1.3ES2 cells were treated with or without TGF-β1 for 6 days. (A) Total DNA was extracted followed...
<p>The indicated cell lines were seeded onto 6-well plate and infected with AdDHBV1S at a MOI of 10....
<p>HepG2 cells, with (241, lanes 2, 5, 8, 11, 14; 245, lanes 3, 6, 9, 12, 15) or without (WT, lanes ...
<p>DSL212 cells were seeded in 6-well plates and cultured in the presence of tetracycline (1 μg/ml) ...
<p>Cell lines used in this experiment are CHO-K1 and its derived cell line Xrs-5 harboring defective...
<p>Dstet5 cells were treated and harvested as depicted in the top panel. DHBV mRNA (A), cytoplasmic ...
<p>Cells were mock infected or infected with HBV at indicated inoculum size (vge/cell) in the presen...
<p>HEK293T cells were cotransfected with pCMV-DHBV/C-, which expresses a core-defective DHBV genome,...
<p>Dstet5 cells were treated and harvested as depicted in the top panel. DHBV mRNA (A), cytoplasmic ...
AbstractAll tissue culture systems for propagating HBV employed so far make use of tandemly arranged...
Related to Fig 4. HepAD38 (DOX-) cells were treated with Bay 41–4109 or GLS4. After 3 days, extracel...
(A) Isolated Smc5 and Smc6 proteins from whole cell lysate, cytoplasmic and nuclear fractions of Hep...
<p><b>(A) Selection of well-performing cell clones.</b> Clones preselected for the presence of HBV D...
<p>(A) and (B). HEK293 cells in 6 cm dishes were cotransfected with the envelope-defective HBV (5 μg...
<p>To examine HBV DNA synthesis in core particles with chimeric C variants, the C-deficient mutant a...
<p>1.3ES2 cells were treated with or without TGF-β1 for 6 days. (A) Total DNA was extracted followed...