Embryos with GFP expression in the olfactory pit region were selected for further analyses, and differentiated neurons were detected by HuC/D antibody staining.
Across all analyses, three associations were found between markers and heading date (Figure 2), two of which were detected by haplotype analyses only.
Although some metabolic differences were detected by analysing subjectively chosen spectral regions, discrimination between the two pathologies and controls would not have been possible if based solely on these major metabolites.
BCR-ABL transcripts were detected by analysing BM with nested reverse transcriptase PCR before 2004 and with quantitative real-time PCR after 2004.
Green fluorescence (sunitinib) and red fluorescence (Lysotracker) were detected by analysing random fields at × 40 magnification using a BX51 fluorescence microscope (Olympus, Milan, Italy).
Of these 67 QTL, 47 were detected by single-QTL analyses and 20 by multiple-QTL analyses, which underlines the importance of using different statistical models.
The metabolic intermediate products were detected by GC/MS analyses of the anode solution.
Moreover, no consistent results were obtained from the study with mature sesame, as well as no obvious proteases were detected by zymographic analyses under our experimental condition (data not shown).
Five endoglucanase proteins in BG- (Eg1, Eg2, Eg3, Eg5, and Eg6) and four each in cellulose- (Eg2, Eg3, Eg4, and Eg5) and RS- (Eg1, Eg2, Eg3 and Eg5) grown cultures, respectively, were detected by zymogram analyses (Figure 5).
Components of Cs or Sr K X-rays were detected by EDXRF analyses of the cells exposed to 75 mM Cs or Sr for 24 h when compared to the control cells, not exposed to Cs or Sr, clearly confirming the accumulation of these metals by the test organism (Additional file 4: Fig. S4).
