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Western blot analyses demonstrate that BACE-1 and IDE levels were increased in cholesterol-fed rabbit retinas.
In summary, the molecularly defined deletion of the JmjC domain in UtxΔ and these western blot analyses demonstrate that Utx Δ is a demethylase null mutation.
Reciprocal immunoprecipitation and western blot analyses demonstrate that SIRT3, but not the other SIRTs tested, binds to SOD2 (Fig 2B D).
Our quantitative Western blot analyses demonstrate that WRN expressed in yeast at levels comparable to that previously reported in several human cell lines was sufficient to restore growth in the sgs1 top3 mutant as detected by plate streak studies or liquid culture growth analysis.
Northern blot analyses demonstrate that mRNA for subunits β3 and β4 is detectable in human testis (Brenner et al., 2000), and it has been shown that the resistance to IbTX and ChTX is determined by the large extracellular loop of the β4 subunit (Meera et al., 2000).
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Western blot analyses demonstrated that Gs-alpha is expressed in differentiating ES cells during EB formation with expression evident in EBs at both day 4 and 20 (Fig. 4A).
Western blot analyses demonstrated that WRN expression was dependent on the concentration of gal in the media.
Western blot analyses demonstrated that stathmin was expressed at high levels in all tested cell lines (Fig 1A).
The western blot analyses demonstrated that all three sigma-2 ligands induced PARP-1 cleavage in both cell lines.
Western blot analyses demonstrated that STAT3 (T705) was strongly activated already at 15 min after stimulation and that it remained constantly activated until 1 h poststimulation.
We also included the complemented strains in the western blot analyses, demonstrating that the complementation restored the expression of the protein.
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