In this model, the equilibria on the theoretical plate are mutually conditional on all components being present in both the solution and the stationary phase.
When, instead, purposely added acid is not present in solution, both reaction pathways ought to be considered.
Real debate, back-and-forths, etc., can be tough to streamline and present in digital solutions.
Dihydroethidium (HEt, 10 µM) was present in all solutions throughout the experiments.
Protease inhibitors (10 μM E-64 and 40 μM leupeptin) were present in all solutions.
For △omcA-△mtrC mutant, the 1712 cm−1 band is present in both water and deuterated water solution.
To avoid accumulation of oxidized products, HEt was not preincubated, but was present in solutions throughout the experiments both in glio-neuronal co-cultures and explants slice cultures.
We find excellent agreement between the methyl C chemical shifts and the side chain rotamers that are present in the solution structures of both complexes (binary KIX·MLL and ternary KIX·MLL·pKID), suggesting the conformation that is present in the NMR structural bundles represents the most populated rotameric state of isoleucine, leucine, and valine residues in all cases.
This is an equilibrium reaction in which a mixture of both compounds is present in the solution.
Both americium and curium are present in solutions mostly in the +3 valence state; whereas americium oxidizes to soluble Am(IV) complexes, curium remains unchanged and can thus be isolated by repeated centrifugation.
Both Am and Cm are mostly present in solutions in the +3 valence state; whereas curium remains unchanged, americium oxidizes to soluble Am(IV) complexes which can be washed away.
