The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by the analyses of a soil bacterial and archaeal community using both clone library and T-RFLP methods. The PCR amplification and microbial community structure patterns were compared among the primers labeled with and without fluorescent groups. PCR amplification was negatively affected by the labeling groups of the primers, which may be caused by the increment of primer molecular weight. It is known that thermodynamic movement of molecules will be slowed as molecular weight increased. Therefore it is understandable that the reaction of primer-DNA template hybridization will be inhibited with the fluorescent groups added to the primer(s). An effec...
<p>Sequences of the primers, and annealing temperatures for the Real Time PCR of the genes studied.<...
Despite the wide-spread use of the polymerase chain reaction (PCR) in various life-science applicati...
<p>Real-time PCR optimization varying annealing temperature and primer concentration.</p
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
<p>(A) Principal component analysis of all PCR settings tested. (B) Differential abundance analysis ...
<p>Species-specific and ubiquitous real-time PCR primers for 6 pathogens, the annealing temperature,...
DNA barcoding employs sequence variation in short, standardized gene regions as a tool to discrimina...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
The success of PCR is partly based on its exponential amplifica-tion characteristics. Nevertheless, ...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
<p><b>Copyright information:</b></p><p>Taken from "Selection strategy and the design of hybrid oligo...
Abstract Microbial ecology studies often use broad-range PCR primers to obtain community profiles. C...
Despite the wide-spread use of the polymerase chain reaction (PCR) in various life-science applicati...
<p>Sequences of the primers, and annealing temperatures for the Real Time PCR of the genes studied.<...
Despite the wide-spread use of the polymerase chain reaction (PCR) in various life-science applicati...
<p>Real-time PCR optimization varying annealing temperature and primer concentration.</p
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
<p>(A) Principal component analysis of all PCR settings tested. (B) Differential abundance analysis ...
<p>Species-specific and ubiquitous real-time PCR primers for 6 pathogens, the annealing temperature,...
DNA barcoding employs sequence variation in short, standardized gene regions as a tool to discrimina...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
The success of PCR is partly based on its exponential amplifica-tion characteristics. Nevertheless, ...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
<p><b>Copyright information:</b></p><p>Taken from "Selection strategy and the design of hybrid oligo...
Abstract Microbial ecology studies often use broad-range PCR primers to obtain community profiles. C...
Despite the wide-spread use of the polymerase chain reaction (PCR) in various life-science applicati...
<p>Sequences of the primers, and annealing temperatures for the Real Time PCR of the genes studied.<...
Despite the wide-spread use of the polymerase chain reaction (PCR) in various life-science applicati...
<p>Real-time PCR optimization varying annealing temperature and primer concentration.</p