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We have further investigated the effectiveness of a gene cassette, which is approximately half the size of the linearized plasmid DNA; pcr-DNA was even less effective than l-DNA, even though the number of gene-encoding templates was expected to be twice that of l-DNA or c-DNA (per unit mass basis exposed to the cells).
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The template is expected to produce a 66-base transcript.
The quantity of selected nontagged template is expected to be lower since interactions will also occur between two tagged RNAs and two nontagged RNAs.
We used four different concentrations of template DNA (0.05, 0.5, 5, and 50 ng) to obtain a broad spectrum of mutation frequencies as the lower concentrations of the template are expected to give rise to higher mutation rates.
Most businesses and leaders took the same approach to managing that growth: They provided employees templates that delivered what was expected.
The MethyLight probes in the present study were able to detect 10% change of DNAm rate of template mixture, and it was expected to be extremely accurate.
This surface area is more than double the surface area of as-received AAO templates which is expected given the tubular morphology46.
We next aimed at growing Au tips from the central cores, using the radial mesopores as templates, which were expected to enhance SERS performance through formation of regions with high electric field enhancement at sharp features, while localizing analyte molecules at such hot spots.
While RT dilution seems the easiest way to overcome this inhibition, as has been widely recommended to augment qPCR amplification success [5], [12], [13], [14], this strategy has the negative consequence of reducing the number of available template copies, and is thus not a suitable alternative when template molecules are expected to be minimal.
Thus, a relatively larger transfer of magnetization was observed in the solute when bound to the molecularly imprinted polymer at a position where multiple hydrogen bonds between the analyte and the template can be expected to take place in the molecularly imprinted polymer only.
Since lesions in the ancient DNA template would be expected to be non-reproducible from different extracts [30] and artifacts at a given site caused by low fidelity of polymerase and sequencing error, as well as jumping PCR [31], [32], were detectable across clones, two independent extractions and cloning sequencing were conducted.
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