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SP (Fansidar; Roche) and the locally manufactured SP were analyzed for quantity of active ingredient by using in vitro dissolution testing protocols according to procedures outlined in the United States Pharmacopeia and by high-performance liquid chromatography (HPLC).
SNPs in DWARF (D) and SELF-PRUNING (SP) were analyzed using the dCAPS and CAPS methods, respectively.
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SPs were analyzed for unpredictable and predictable response processing.
In implicit conditions, slow cortical potentials (SPs) were analyzed to reflect the amount of controlled processing and the localization of activated neural task representations.
To characterize the changes of SP topography from the session before sleep to after sleep independently of individual variations in SP magnitude min-max normalized values of SPs were analyzed.
All identified putative signal peptides (SPs) were analyzed using the Signal P 3.0 server [ 68].
Cell-surface markers and side populations (SPs) were analyzed using flow cytometry.
The SPs were analyzed by their characteristic fluorescent profiles in dual-wavelength analysis, in which the Hoechst 33342 dye was excited with a UV laser at 350 nm, and fluorescence emission was measured using 450 DF10 (450/20 nm band-pass filter) and 675LP (675 nm long-pass edge filter) optical filters.
The relationship between factors and SPs was analyzed.
An experiment based on the stated preferences (SP) was carried out with the drivers, and the SP data were analyzed using an ordered probit (OP) model.
SP-B and SP-C were analyzed using ELISA techniques as described previously [ 24, 25].
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