Additional file 6: Figure S3. Profiling of the expression of SvCAD3, SvCAD5, SvCAD6 and SvCAD7 following normalisation with the most suitable, and the least suitable, set of reference genes. AâD RT-qPCR data to profile the expression of SvCADs, SvCAD3 (A; Sevir.6G025000), SvCAD5 (B; Sevir6G024400), SvCAD6 (C; Sevir7G014100), and SvCAD7 (D; Sevir7G245600) was normalised using the set of the three most suitable reference genes (ASPR6, DUSP and PP2A) and with the set of the three least suitable reference genes (FBoxD, PGM and SEIPIN)
Additional file 5: Table S1. The primer features of candidate reference genes and their PCR efficien...
<p>For the target genes, the real-time qRT-PCR derived relative expression levels (A, D and G for OP...
<p>Details of primer pairs and amplicon size of reference genes used for normalization of qRT-PCR da...
Additional file 3: Table S2. Â Selection of reference gene candidates for normalisation of S. viridi...
Additional file 2: Table S1. Table of reference gene candidates and the primers used for subsequent ...
Additional file 5: Figure S2. Analysis of Setaria viridis CAD gene expression according to the RNA-S...
Additional file 1: Figure S1. Setaria viridis tissues sampled for RT-qPCR analysis. Setaria viridis ...
Additional file 1: Table S1. Ct values of the 9 candidate reference genes. Figure S1. Specificity of...
Employing reference genes to normalize the data generated with quantitative PCR (qPCR) can increase ...
<div><p>Employing reference genes to normalize the data generated with quantitative PCR (qPCR) can i...
Background: A critical step in the RT-qPCR workflow for studying gene expression is data normalizati...
<p>A) Expression stability measurements (M) for the five reference genes analyzed. The x-axis from l...
Additional file 3: Table S2. Primer pairs sequences, amplicon size (A) in basepairs (bp), melting te...
Additional file 1: Fig. S1. Variation in the expression of reference genes using distribution of cyc...
Reverse transcription and real-time PCR (RT-qPCR) has been widely used for rapid quantification of r...
Additional file 5: Table S1. The primer features of candidate reference genes and their PCR efficien...
<p>For the target genes, the real-time qRT-PCR derived relative expression levels (A, D and G for OP...
<p>Details of primer pairs and amplicon size of reference genes used for normalization of qRT-PCR da...
Additional file 3: Table S2. Â Selection of reference gene candidates for normalisation of S. viridi...
Additional file 2: Table S1. Table of reference gene candidates and the primers used for subsequent ...
Additional file 5: Figure S2. Analysis of Setaria viridis CAD gene expression according to the RNA-S...
Additional file 1: Figure S1. Setaria viridis tissues sampled for RT-qPCR analysis. Setaria viridis ...
Additional file 1: Table S1. Ct values of the 9 candidate reference genes. Figure S1. Specificity of...
Employing reference genes to normalize the data generated with quantitative PCR (qPCR) can increase ...
<div><p>Employing reference genes to normalize the data generated with quantitative PCR (qPCR) can i...
Background: A critical step in the RT-qPCR workflow for studying gene expression is data normalizati...
<p>A) Expression stability measurements (M) for the five reference genes analyzed. The x-axis from l...
Additional file 3: Table S2. Primer pairs sequences, amplicon size (A) in basepairs (bp), melting te...
Additional file 1: Fig. S1. Variation in the expression of reference genes using distribution of cyc...
Reverse transcription and real-time PCR (RT-qPCR) has been widely used for rapid quantification of r...
Additional file 5: Table S1. The primer features of candidate reference genes and their PCR efficien...
<p>For the target genes, the real-time qRT-PCR derived relative expression levels (A, D and G for OP...
<p>Details of primer pairs and amplicon size of reference genes used for normalization of qRT-PCR da...