<p>(A) DMD ex51-52.2 assay and (B) DMD ex47-52 assay. The left panels show how the positive droplet populations change with decreasing annealing temperatures. At higher annealing temperatures the overall fluorescence of the positive droplet population (in blue) is lower, caused by a less efficient PCR amplification, and consequently the separation of the positive and negative droplet (in grey) clouds is less pronounced. In the right panels the corresponding concentrations of the constructs along the temperature gradient are represented. The %CV (coefficient of variation) between the different annealing temperatures is 3–4%, indicating a highly consistent quantification of the construct concentration, even at suboptimal amplification conditi...
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
<p>On the left are normalised fluorescence thermal transitions of molecular beacon (pink circles) an...
Applying digital PCR (dPCR) technology to challenging clinical and industrial detection tasks has be...
<p>Droplet populations observed for each duplex assay tested with wild-type and relevant mutant cell...
Digital PCR in droplets (ddPCR) is an emerging method for more and more applications in DNA (and RNA...
<p>A gradient PCR between 50°C and 70°C (a) with EGDe DNA (≈ 10<sup>3</sup> copies/per sample) was p...
The droplet digital polymerase chain reaction (ddPCR) determines DNA amounts based upon the pattern ...
Real-time quantitative polymerase chain reaction (qPCR) depends on precise temperature control of th...
AbstractDigital PCR in droplets (ddPCR) is an emerging method for more and more applications in DNA ...
Amplification curve thresholds for time to positive are indicated in red on graphs A, B and C. A–apr...
(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 "Ultra fast miniaturized real-time PCR: 40 cycles ...
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
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>On the left are normalised fluorescence thermal transitions of molecular beacon (pink circles) an...
Applying digital PCR (dPCR) technology to challenging clinical and industrial detection tasks has be...
<p>Droplet populations observed for each duplex assay tested with wild-type and relevant mutant cell...
Digital PCR in droplets (ddPCR) is an emerging method for more and more applications in DNA (and RNA...
<p>A gradient PCR between 50°C and 70°C (a) with EGDe DNA (≈ 10<sup>3</sup> copies/per sample) was p...
The droplet digital polymerase chain reaction (ddPCR) determines DNA amounts based upon the pattern ...
Real-time quantitative polymerase chain reaction (qPCR) depends on precise temperature control of th...
AbstractDigital PCR in droplets (ddPCR) is an emerging method for more and more applications in DNA ...
Amplification curve thresholds for time to positive are indicated in red on graphs A, B and C. A–apr...
(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 "Ultra fast miniaturized real-time PCR: 40 cycles ...
The influences of fluorescence labeling on PCR amplification and T-RFLP analysis were examined by th...
(A) Agarose gel electrophoresis images of PCR mixtures at various annealing temperatures (30–55°C) u...
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>On the left are normalised fluorescence thermal transitions of molecular beacon (pink circles) an...
Applying digital PCR (dPCR) technology to challenging clinical and industrial detection tasks has be...