Your English writing platform
Discover LudwigExact(1)
Each of the transposon and transposase plasmids will be verified for sequence identity and DNA integrity.
Similar(59)
The sequence integrity of all constructs described in this study was verified for sequence integrity by nucleotide sequencing.
Whereas both human and mouse 3' UTR of SPP1 are the target of several microRNA, retrieved by an in silico search (; data not shown), this hypothesis remains to be verified for the bovine SPP1 3' UTR sequences.
The mutations were contained in the BlpI/SacI fragment, and the sequence of this fragment was verified for each mutant by automated sequencing at the University of Virginia Biomolecular Research Facility.
This finding has been verified for the whole receptor sequences.
The inserted sequence was verified for the presence of the mutation and absence of PCR errors by DNA sequencing.
Sequence was verified for specificity using blast on the National Center for Biotechnology Information (NCBI) website (http://www.ncbi.nlm.nih.gov/BLAST/) and a 465 base pairs (bp) sequence was chosen to target the 5′ end of the 10·2 Kb DNA fragment containing the MIF gene.
The contig sequences were removed, and the remaining protein sequences were verified for the presence of the typical bZIP domain using Pfam with an E-value cutoff < 1.0.
AID activity was verified for Ela1 by conventional Sanger sequencing (Table 1).
After extraction the plasmid was verified for the correct insert by sequencing and quantified as described (7 ).
Matches between germline and tumor DNA were verified for all samples by direct sequencing of 26 single nucleotide polymorphisms (SNPs) at 24 loci (data not shown).
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