<p>The y-axis indicates fold change in expression among the samples. The Lg (Relative Quantitation) of the genes in the sepals was calibrated as zero. Error bars indicate the standard deviation of the mean (SD) (n = 3). Three replicates were analyzed, with similar results. a, b, and c, d, one way ANOVA with Bonferroni multiple comparison test significant at P<0.05 between two of the individual floral organs sepal, petal, Labellum, gynostemium.</p
<p>Col in sterile culture was chosen for gene expression analyses. The samples were harvested at 8 D...
Additional file 2. Fig. S2. Quantitative RT-PCR of B and E genes showing general expression across J...
<p>Error bars indicate standard deviations (n = 3). 1, primary root; 2, pericarp; 3, internode; 4, a...
<p>Up- and down-regulated transcripts were quantified. The results of six comparisons between each t...
<p>(A) Gene expression data obtained through RNA-Seq analysis. (B) Real time RT-PCR analyses of gene...
<p>Expression analysis in different organs (A) and during flower development (B). Le, leaves; St, st...
<p>Up- and down-regulated transcripts were quantified. The results of six comparisons between each t...
<p>Mock infected plants were used to normalize fold change of early and late samples in leaf and tub...
Quantitative real time (qRT)-PCR is a precise and efficient method for studying gene expression chan...
<div><p>Quantitative real time (qRT)-PCR is a precise and efficient method for studying gene express...
<p>RT, ST, RI, SI, and YL represent the rhizome tip, shoot tip, rhizome internodes, shoot internodes...
<p>Expression pattern of key structural genes in chrysanthemum petals with different flower colour b...
Quantitative real time (qRT)-PCR is a precise and efficient method for studying gene expression chan...
<p>Relative mRNA levels of individual genes normalized to <i>UBQ5</i> are shown. Y-axis shows the re...
<p>(A) Relative expression levels of MADS box genes expressed across floral organs. (B) Relative exp...
<p>Col in sterile culture was chosen for gene expression analyses. The samples were harvested at 8 D...
Additional file 2. Fig. S2. Quantitative RT-PCR of B and E genes showing general expression across J...
<p>Error bars indicate standard deviations (n = 3). 1, primary root; 2, pericarp; 3, internode; 4, a...
<p>Up- and down-regulated transcripts were quantified. The results of six comparisons between each t...
<p>(A) Gene expression data obtained through RNA-Seq analysis. (B) Real time RT-PCR analyses of gene...
<p>Expression analysis in different organs (A) and during flower development (B). Le, leaves; St, st...
<p>Up- and down-regulated transcripts were quantified. The results of six comparisons between each t...
<p>Mock infected plants were used to normalize fold change of early and late samples in leaf and tub...
Quantitative real time (qRT)-PCR is a precise and efficient method for studying gene expression chan...
<div><p>Quantitative real time (qRT)-PCR is a precise and efficient method for studying gene express...
<p>RT, ST, RI, SI, and YL represent the rhizome tip, shoot tip, rhizome internodes, shoot internodes...
<p>Expression pattern of key structural genes in chrysanthemum petals with different flower colour b...
Quantitative real time (qRT)-PCR is a precise and efficient method for studying gene expression chan...
<p>Relative mRNA levels of individual genes normalized to <i>UBQ5</i> are shown. Y-axis shows the re...
<p>(A) Relative expression levels of MADS box genes expressed across floral organs. (B) Relative exp...
<p>Col in sterile culture was chosen for gene expression analyses. The samples were harvested at 8 D...
Additional file 2. Fig. S2. Quantitative RT-PCR of B and E genes showing general expression across J...
<p>Error bars indicate standard deviations (n = 3). 1, primary root; 2, pericarp; 3, internode; 4, a...