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Results suggested that the main effect that differentiates the free enzyme and the two derivatives analyzed was of diffusive nature.
Dispersions of the different cellulosic derivatives analyzed provide oleogels with a wide variety of rheological properties, thermal stability and physical appearance.
The results obtained imply that different ionic liquids interact in a comparable way with the iodinated derivatives analyzed here as the retention times in the second dimension are similar.
The C-terminally deleted Mec1 proteins were less abundant in crude protein lysates, and all of the derivatives analyzed were unstable in cell extracts prepared in the absence of protease inhibitors.
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The conformations of the two cyclic salinomycin derivatives were analyzed by ROESY spectrum in DMSO-d6, indicating derivative 7 may adopt more appropriate conformations for the coordinate with alkali metal ion than derivative 5, which has a closer distance between H3 and H25.
Secondary structure of the resultant derivatives was analyzed by computer simulation and circular dichroism, exhibiting that the hydrophobic derivatives had a propensity to form high content of helix and entered corneal and conjunctival cells more easily than did penetratin.
In order to reveal whether hESC derived NPs have the potential to produce PNS derivatives we analyzed the expression of several early and late PNS markers in hNPs at the prime of their neuronal potential as explained above.
The structure activity relationships (SARs) of the derivatives were analyzed.
Structure activity relationships of these derivatives were analyzed.
The electrochemical properties of BODIPY derivatives were analyzed using cyclic voltammetry.
The APA derivatives were analyzed by GC MS and MS/MS using negative ion chemical ionization.
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