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We then removed the transposons to obtain transgene-free neuronal precursors and neurons.
We then removed all restraints for a second round of equilibration.
We then removed entries without chemical structures, such as some herbal extracts and vaccines.
We then removed residues 20 44 of cytSec61β and found that the mutant failed to tangle the ER and microtubules (Fig. 1F and 1G).
We then removed males' swords and retested escape performance.
We then removed the sequences with one or more ambiguous nucleotide sequences within the HA1 region and deleted identical sequences.
We then removed the worms and allowed the embryos to develop prior to counting viable and inviable progeny.
We then removed the vast majority of connection so that on average there remained only 10 connections per node.
We then removed redundant gene/probe sets taking into account the ENTREZ, Unigene and RefSeq gene-id annotations.
We then removed the inoculum and overlaid the cells with a 1.2% solution of methylcellulose in a final concentration of 1X DMEM, 2.5% FBS.
3) If any possible artifact waveforms were still left, we then removed them during the preprocessing of spike waveforms using Plexon Offline Sorter because artifact waveforms were highly distinct from neuronal spike waveforms.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com