<p>Two representative gel pictures are shown. All bands were gel extracted and subject to sequencing and cloning and sequencing from both directions. Arrows indicate the band that contained the HBoV head-to-tail sequences.</p
<p>Arrows indicate DNA fragments positions. (A) Lane M: D2000 DNA marker, lane 1: GS fragments, lane...
Gels showing detection of PCR amplicons of isolates with mutations V135A (A) and P253S (B), respecti...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
<p>A: PCR products from real-time PCR experiments were analyzed on a 3% agarose gel. Lanes: 1: TaqMa...
Primers 4-Fw and Nuc-Rv were used. Amplicons were electrophoresed before or after digestion with Cla...
<p>The gels from the top to the bottom show products from the primary, secondary, and tertiary react...
<p>Putative mutations in the pools (1, 2, 3, 4) are identified by the presence of two bands (indicat...
(A-D) Gels of PCR products resulting from outer and nested inner PCR amplification of the intact pro...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
<p>Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expected ...
<p>Electrophoreses were run in 1 x TAE at 60 V for 40 min. Lanes M and M2: DNA marker I and pUC19 DN...
<p>PCR-RFLP agarose gel (A) after digestion with Taq1B enzyme. The 1000 bp band corresponds to the B...
<p>Note: Nucleotides underlined are HBoV1 sequences or sequences complementary to the HBoV1 sequence...
<p>A: The PCR product amplified from the genomic DNA using the gB primers (Lane 1) and negative cont...
<p>Lanes in the first row (118 to 136) were loaded with PCR products of FGTB patients; Lanes in the ...
<p>Arrows indicate DNA fragments positions. (A) Lane M: D2000 DNA marker, lane 1: GS fragments, lane...
Gels showing detection of PCR amplicons of isolates with mutations V135A (A) and P253S (B), respecti...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...
<p>A: PCR products from real-time PCR experiments were analyzed on a 3% agarose gel. Lanes: 1: TaqMa...
Primers 4-Fw and Nuc-Rv were used. Amplicons were electrophoresed before or after digestion with Cla...
<p>The gels from the top to the bottom show products from the primary, secondary, and tertiary react...
<p>Putative mutations in the pools (1, 2, 3, 4) are identified by the presence of two bands (indicat...
(A-D) Gels of PCR products resulting from outer and nested inner PCR amplification of the intact pro...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
<p>Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expected ...
<p>Electrophoreses were run in 1 x TAE at 60 V for 40 min. Lanes M and M2: DNA marker I and pUC19 DN...
<p>PCR-RFLP agarose gel (A) after digestion with Taq1B enzyme. The 1000 bp band corresponds to the B...
<p>Note: Nucleotides underlined are HBoV1 sequences or sequences complementary to the HBoV1 sequence...
<p>A: The PCR product amplified from the genomic DNA using the gB primers (Lane 1) and negative cont...
<p>Lanes in the first row (118 to 136) were loaded with PCR products of FGTB patients; Lanes in the ...
<p>Arrows indicate DNA fragments positions. (A) Lane M: D2000 DNA marker, lane 1: GS fragments, lane...
Gels showing detection of PCR amplicons of isolates with mutations V135A (A) and P253S (B), respecti...
<p>(A) Agarose gel (2%) electrophoresis showing amplification of a specific PCR product of the expec...