Sentence examples for mutants at a from inspiring English sources

Fig. 7 Oxidation of benzopyrene by CueO and its mutants at a pH 3.5 and 30 °C, and b pH 3.5 and 60 °C.

To analyze the unfolding process of active AQN mutants at a fixed temperature, changes in the CD spectra of the wild-type enzyme, D17N, E237Q, D212N or D183N as a function of time were recorded at 70°C and 80°C.

The low copy number wild type was able to back invade the higher copy mutants at a much smaller copy number when non-conjugal plasmids were present.

Initial populations are clonal, but at division, each clone generates mutants at a rate μ that differ in fitness from the parent clone.

Probability generating function is used to study the probability of colony extinction, probability of treatment success, and the probability of having resistant mutants at a given colony size.

These mutants are brighter throughout the exponential phase of growth in contrast to WT, which only reaches the same level of luminescence as these mutants at a high cell density.

Mutagenesis and screening of 11,000 mutants at sites A-G generated ~500 mutants with higher activity toward carboxymethyl cellulose (CMC) after pre-incubation at 50°C for 45 min than the wild-type TrEGI expressed using cell-free synthesis.

The classification of mutants based on secondary structure (helix, strand, turn and coil) and solvent accessibility (buried, partially buried, partially exposed and exposed) distinguished the stabilizing/destabilizing mutants at an average accuracy of 81% and 80%, respectively for ΔΔG and ΔΔGH2O.

Trypsin cleaved the native (folded) form of each mutant at a unique site defined by the insert.

Further, the alterations in response to insertions are very similar for each mutant at a given site.

Reduced targeting in IGL and misrouted fibers also exist in 50% Dab1 mutant at a less modest degree compared to reln −/− mice, while in the other half, only misrouted axons are found, again less than those in reln −/− mutant.