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The samples containing Oragene·DNA/saliva mixed were then taken to a laboratory where their transparency was examined, after which they were stored at room temperature until processing (after 3 days or 8 months later).
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The predictions of inversion velocity, i.e. the velocity at which the bed is homogeneously mixed, are then compared to available experimental data.
A mixed linear approach (SAS, Procedure MIXED) was then used to determine whether the morphological traits changing with time to first flower had a significant effect on PPR.
The mixed powders were then made into cylindrical samples using a commercial LENS™-750 system.
The mixed solutions were then all expanded to 100 ml with ethanol.
The solubilization capacities of vitamin E and vitamin E acetate in the mixed micelles were then compared.
The mixed PLAs were then formed into sheets by compression molding before leaching in water for 48 h.
The mixed samples were then extracted with 1.5 mL of dichloromethane: n-Hexane (1 2), by vortex mixing for 2 min.
The mixed samples were then bisulfite treated and subjected to our PMA LINE-1 (LINE) and Alu (SINE) assays.
The mixed cultures were then treated with CPA, trypsinized and reseeded.
Nondauer mixed stages were then purified on day 8 or 9 and used for RNA extraction.
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