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The mutants were stable over several days at room temperature.
Mutants were stable with respect to both characters.
Besides, the mutants were stable over the pH range of 5.0 9.0 as TsPOx, but generally retained greater activities (Fig. 2b).
USP25m full-length as well as the UBD deletion mutants were stable at 16 hours treatment, supporting mono- and multi-Ub modification.
In agreement, several of the differentially expressed transcripts in the three mutants were stable RNAs (rRNAs, tRNAs and sRNAs).
Our data showed that target gene restoration (TGR) occurred in IDM mutants, even in the presence of antibiotics, while the IFD mutants were stable.
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By contrast, the surfactant activity of AChE586-599 and the other mutants was stable, which suggests that they remained stably associated with the air-water interface during the length of the time course.
The expression analysis revealed that all mutants are stable (Fig. 6).
By three criteria [expression, stability after purification, and BN-PAGE after DDM/urea extraction], the majority of the Trp mutants are stable proteins suitable for analysis.
A striking difference between ∆ pnp mutant, ∆ rnb and ∆ rnr mutants was the fact that many of the differentially expressed transcripts in ∆ pnp mutant were stable RNAs (tRNAs, rRNAs and sRNAs).
Furthermore, the F230A mutant was stable during the oxidation of other phenolic compounds, including m-cresol and 3-methoxyphenol.
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