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All conclusions discussed in the text are supported by separate analyses using reduced datasets in which all indels were removed (data not shown).
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In accordance with guidelines for the use of the SF-36v2® health survey, the a priori analysis using a total score was replaced post hoc by two separate analyses using PCS and MCS scores.
We conducted two separate analyses using two distinct data sets.
Student and mentor interviews were analysed in two separate analyses using an inductive thematic approach.
The Mantel permutation test was used to correlate pair-wise Φst values obtained by separate analyses of the AFLP, ISSR and combined data sets with geographic distance.
A substantial amount of heterogeneity was explained by separate analyses of groups of trials.
Combined trial analyses were followed by separate analyses of the E and E + P trial data.
Bound proteins were eluted in SDS sample buffer, separated by SDS-PAGE and visualized by Coomassie Blue staining and Western analyses using α-eS26 antibody.
Bound proteins were eluted in SDS sample buffer, separated by SDS-PAGE and visualized by Coomassie Blue staining and Western analyses using α-GFP antibody.
Bound proteins were eluted in SDS sample buffer, separated by SDS-PAGE and visualized by Coomassie Blue staining and Western analyses using α-eS26 antibodies.
After washing, bound proteins were eluted in SDS sample buffer, separated by SDS-PAGE, and visualized by either Coomassie Blue staining or Western analyses using indicated antibodies.
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