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When assayed for leukaemic regeneration in NOD/SCID/γ mice, genetically diverse 'stem' cells read-out, broadly reflecting the clonal architecture.
When assayed for their ability to grow in soft agar, Ras-transduced cyclin D1-HA/FHL2−/− cells formed colonies at similar efficiency as wt MEFs (0.04%), whereas no colony was detected in cyclin D1-HA/FHL2−/− cells infected with the empty vector (Fig. 6C).
When assayed for CTL activity, the CTL population generated by viral infected CMT.TAP1,2/Kb cells at the lowest dose showed a killing activity significantly greater than the CTL population generated at the equivalent m.o.i using viral-infected CMT.64 cells (Fig. 4B).
Plants were approximately 6 weeks old when assayed for ploidy.
However, when assayed for transport with [H]MTX, all replacements were poorly tolerated.
In contrast, when assayed for rDNA-silencing defects, nab3 mutants displayed a strong defect, similar to that observed in esa1.
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Furthermore, when assaying for sensitivity to H2O2, the DRE2-TAH18 fusion expressing strain was significantly more resistant than wild-type (as shown in figure 5-E).
Though the greatest difference in hydrolytic activity was seen between the mature CD34DCs and the immature MDDCs when assaying for β-glucuronidase activity, this difference was at most 5-fold, substantially less then the 28-fold difference in protease activity between these two DC types (Fig. 3B).
When assaying for Id2 mRNA, however, both Wnt3a and BMP4 significantly increased transcript levels.
When assaying for higher order complex formation, GSQUA proteins showed greater activity.
This step was excluded when assaying for active TGFβ1 within the cell culture supernatant.
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