A quantity of 60 mg was resolved in 1 ml of distilled water, resulting in a concentration of 0.05 M.
A 1-ml aliquot of the 20× concentrated cell medium with nascent HDL was resolved into 1-ml fractions on a calibrated HiLoad 16/60 Superdex 200 gel-filtration column (GE Healthcare, Mickleton, NJ, USA).
For thin-layer chromatographic (TLC) analysis, 0.1 g purified-rhamnolipids was resolved in 1 ml chloroform.
The polysaccharide-dye complex precipitated and was resolved in 1 ml dissociation reagent.
The precipitate was resolved in 3 mL of grinding medium and applied to an sucrose density gradient consisting of the following layers: 4 mL 60%, 5 mL 57%, 7 mL 52,5%, 7 mL 47%, 5 mL 43%, 5 mL 35%.
The precipitate was resolved in 200 mL of 0.01% formic acid in acetonitrile : water (1 : 1) solvent and injected for MS/MS analysis.
Exactly 100 g of the husk extract was resolved into 200 ml of sterile distilled water and poured in a separatory funnel and extracted in succession with organic solvents according to order of polarities, starting with the least polar solvent.
The BI tree recovered an identical topology, except that one branch that was resolved in the ML tree collapsed to a trichotomy in the BI tree (see Figure 1).
The genus Bambusa was resolved as monophyletic with 83% ML bootstrap support with very short branches and one internal node with 81% ML bootstrap support.
The rosid clade (excluding Vitaceae) was resolved with 66% BS support in the ML tree.
