<p>Multiplexed TaqMan assays were performed for the quantification of iron homeostasis genes as indicated (FAM labeled) and the control, RAD23-3 (VIC labeled) after reverse-transcription of mRNA extracts from control and <i>wbc19</i> mutant plants germinated on MS media with or without 50 mg/l kanamycin. Data shown are from 4 biological replicates and 3 technical replicates. Error bars indicate standard deviation.</p
<p>The gene expression was determined by Real Time reverse transcriptase PCR normalized to the house...
<p>RNA harvested from WT-Y cells was used to prepare cDNA for qRT-PCR analysis of representative gen...
<p>Quantitative RT-PCR analyses of a few candidate genes: Metallothionein, NAM-1, LEA-12, and Sec-E....
<p>Relative gene expression (A) in 2.4.1Δ<i>irr</i> under normal iron conditions compared to the wil...
Quantitative RT-PCR analysis of α-zein regulator genes in 20-DAP endosperm. Gene expression was norm...
<p>Relative transcript abundance was measured by quantitative real-time PCR (qRT-PCR) and normalized...
Relative expression levels of selected ten genes and 18S as an internal reference detected by RT-qPC...
<p>8-day-old plants were grown on 1/2 MS without iron (black) or supplemented with 100 µM Fe (white)...
<p>Mock infected plants were used to normalize fold change of early and late samples in leaf and tub...
<p>Data were normalized against a reference of wintersweet actin and tubulin genes. All quantitative...
<p>QRT-PCR data were obtained from four independent cultures of ATCC 33277/pTCOW and TR719 per hemin...
<p>(A) Semiquantitative RT-PCR analysis of <i>OsCESA9</i> expression. (B) Real-time RT-PCR analysis ...
<p>(A) RT-PCR detection of TRV RNA in upper un-injected leaves. (B) qPCR analysis of <i>SlAGO1-1</i>...
<p>The cultures were subjected to iron deprivation in the presence of 10 µM 2,2′-dipyridyl. Total RN...
<p>The signal intensity of each unigene was normalised against 18S rRNA as a housekeeping gene. The ...
<p>The gene expression was determined by Real Time reverse transcriptase PCR normalized to the house...
<p>RNA harvested from WT-Y cells was used to prepare cDNA for qRT-PCR analysis of representative gen...
<p>Quantitative RT-PCR analyses of a few candidate genes: Metallothionein, NAM-1, LEA-12, and Sec-E....
<p>Relative gene expression (A) in 2.4.1Δ<i>irr</i> under normal iron conditions compared to the wil...
Quantitative RT-PCR analysis of α-zein regulator genes in 20-DAP endosperm. Gene expression was norm...
<p>Relative transcript abundance was measured by quantitative real-time PCR (qRT-PCR) and normalized...
Relative expression levels of selected ten genes and 18S as an internal reference detected by RT-qPC...
<p>8-day-old plants were grown on 1/2 MS without iron (black) or supplemented with 100 µM Fe (white)...
<p>Mock infected plants were used to normalize fold change of early and late samples in leaf and tub...
<p>Data were normalized against a reference of wintersweet actin and tubulin genes. All quantitative...
<p>QRT-PCR data were obtained from four independent cultures of ATCC 33277/pTCOW and TR719 per hemin...
<p>(A) Semiquantitative RT-PCR analysis of <i>OsCESA9</i> expression. (B) Real-time RT-PCR analysis ...
<p>(A) RT-PCR detection of TRV RNA in upper un-injected leaves. (B) qPCR analysis of <i>SlAGO1-1</i>...
<p>The cultures were subjected to iron deprivation in the presence of 10 µM 2,2′-dipyridyl. Total RN...
<p>The signal intensity of each unigene was normalised against 18S rRNA as a housekeeping gene. The ...
<p>The gene expression was determined by Real Time reverse transcriptase PCR normalized to the house...
<p>RNA harvested from WT-Y cells was used to prepare cDNA for qRT-PCR analysis of representative gen...
<p>Quantitative RT-PCR analyses of a few candidate genes: Metallothionein, NAM-1, LEA-12, and Sec-E....