Within 400 generations, smaller mutants were selected in response to each size selection.
In that case, 10%% of the mutants were selected per mutation operator.
Mutants were selected by serial transfers in AM1 mineral salts medium with 10% xylose.
Mutants were selected by flow cytometric cell sorting with a fluorescent-labeled SEC3.
Mutants were selected that formed dry, compact, small colonies with reddish-violet pigment on regeneration agar plates.
The AChE mutants were selected in order to obtain high resolution, enhanced sensitivity and minimal assay time.
Yeast display libraries of random and site-directed hVβ2.1 mutants were selected for improved domain stability and for higher affinity binding to TSST-1.
Neutralization-resistant mutants were selected from these populations by application of JE-specific virus neutralizing monoclonal antibody (mAb) 503, which possessed a 51,200-fold neutralization titer.
To explore the mechanism of tRNAAla recognition, the bases of the acceptor-stem region were randomized and active mutants were selected in a tRNAAla knockout strain.
To explore the proteomic changes of heritable variant rice plants induced by space environment, three mutants were selected after seed space flight by comparing the phenotypes with their on-ground controls.
The insertion includes a Gal4 sequence that can be used to label the expression pattern of the disrupted gene and 368 mutants were selected because their perturbed-gene expression enriched in the mushroom body.
