Exact(5)
In this study, we found that, upon H2O2 treatment, the caspase activities in tps1△ mutant were much higher than those in wild-type cells, similar to the phenomena of intracellular Ca2+ levels.
Indeed, the levels of the B56 regulatory subunit in IPs of the GFP-BubR1Δ432 484 GFP-BubR1Δ432 484lower than those of the wild-type protein.
The time to peak release for ω-conotoxin GVIA-treated fish and tb204a mutant were much more variable than seen in control fish, but despite the variability both were significantly prolonged when compared to control (p<0.001; Figure 2B).
Moreover, the pollen tubes of the AtrabD2b/2c double mutant were much shorter than those of wild-type plants or either single mutant (P < 0.01), and the single mutants had shorter pollen tubes than wild-type plants.
Additionally, the expression levels of Lipoxygenase (LOX -like and ALOX -likede synthand (Alleneike unigenes indicated that endoxideusynthase of JAOS -likeresistAOS -liket were munigeneser than indicatedld-that.
Similar(55)
The catalytic efficiency for each active mutant was much higher than that of wild-type at low pH.
The optimal concentrations of glucose and yeast extract for cordycepin production of the mutant was much higher than that of control (wild strain) and the cordycepin production was 2.79 times higher.
The induction in the mutant was much slower and less substantial.
Nuclear localization of the G39A mutant was much reduced in general and less than 20% showed nuclear speckles (Figure 6A-C).
In addition, we had also shown that an etk knock-out mutant is much less resistant to polymyxin than a wild-type E. coli K-12 strain.
Moreover, the mutant was much more diffuse throughout the cytoplasm of cells with few to no puncta, and exhibited a prominent reticular pattern suggestive of ER localization.
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