Your English writing platform
Discover LudwigSuggestions(1)
Exact(60)
It was based on cyclic enzymatic signal amplification (CESA) and template-free DNA extension reaction.
Approximately 28.356 kb of foreign gene sequence from CT-4 cosmid and by further PCR extension reaction was obtained.
Then, template-free DNA extension reaction was triggered by terminal deoxynucleotidyl transferase (TdT), producing amounts of single-stranded DNA (ssDNA).
The extension reaction was adjusted on 72 °C for 10 min.
Following amplification of the region of interest, a primer extension reaction was carried out.
Then, the processed beadchip for the single-base extension reaction was stained and imaged on an Illumina Bead Array Reader.
The primer extension reaction was performed with the AMV reverse transcriptase (Promega, Madison, USA) as described previously [12].
A single-nucleotide extension reaction was performed in 2 µg of DNA using the cytosine extension assay described previously [14].
PCR amplification and primer extension reaction were carried out in a DYAD™ PCR thermal cycler (MJ Research).
Furthermore, this hydrolysis product and the synthetic 24-mer served as primers in a sequenase primer extension reaction (lanes 5, 7, Figure 6B).
SNP genotyping was performed on genomic DNA from the 33 phenotyped inbred mouse strains using a single-base extension reaction on the Sequenom genotyping platform.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com