<p>Transcript levels for the genes encoding for the CPS small subunit (<i>LjCarA</i>) and for the large subunit (<i>LjCarB</i>) were quantified by qRT-PCR in WT (black dots, solid line) and mutant (white dots, dashed line) leaves at the time points indicated. Relative transcript levels are reported for each genotype compared to the housekeeping genes. Data are the mean ± S.D. of three independent biological replicates.</p
<p>The qRT-PCR analysis of the expressions of two enzyme-encoding genes in chl degradation pathway (...
Real-time quantitative polymerase chain reaction (qPCR) has become widely used as a method to compar...
Gene expression of PLAT1 in WT roots (A) and leaves (B) was determined between one day and 14 days o...
<p>Transcript levels were quantified by qRT-PCR in WT (black dots, solid line) and mutant (white dot...
<p>Transcript levels were quantified by qRT-PCR in WT (black dots, solid line) and mutant (white dot...
<p>RNA isolated from 10-day-old seedlings were used to quantify gene expression by qRT-PCR. The gene...
<p>RNA was extracted from 4d dark-grown seedlings in different genetic backgrounds. Three biological...
<p><b>A-I: qPCR analysis of gene expression levels</b> in 1 DPA, 3 DPA, and 8 DPA ovules and in leav...
<p>(A) The phenotypes of WT and four leaf coloration mutants grown with or without sucrose. (B) qRT-...
<p><b>(a)</b> Expression of the genes for NAD(H)-GDH (<i>LjGdh1</i>, <i>LjGdh2</i> and <i>LjGdh3</i>...
<p>Total RNA was extracted from 10-day-old WT and <i>atl31–1/atl6–1</i> plants grown under LL and ML...
<p>Expression of <i>SDP1</i>, <i>CTS</i>, <i>LACS6</i>, <i>LACS7</i>, <i>ACX1</i>, <i>ACX2</i>, <i>M...
<p>(a) PCR of genomic DNA showed the successful generation of the T-DNA insertion mutant. (b) RT-PCR...
<p>Transcript levels of these genes in transgenic plants are indicated relative to the level of WT p...
<p>Most transcripts increase less than 2-fold between LP1&2 and LP3&4 in Col, and increase 2-fold or...
<p>The qRT-PCR analysis of the expressions of two enzyme-encoding genes in chl degradation pathway (...
Real-time quantitative polymerase chain reaction (qPCR) has become widely used as a method to compar...
Gene expression of PLAT1 in WT roots (A) and leaves (B) was determined between one day and 14 days o...
<p>Transcript levels were quantified by qRT-PCR in WT (black dots, solid line) and mutant (white dot...
<p>Transcript levels were quantified by qRT-PCR in WT (black dots, solid line) and mutant (white dot...
<p>RNA isolated from 10-day-old seedlings were used to quantify gene expression by qRT-PCR. The gene...
<p>RNA was extracted from 4d dark-grown seedlings in different genetic backgrounds. Three biological...
<p><b>A-I: qPCR analysis of gene expression levels</b> in 1 DPA, 3 DPA, and 8 DPA ovules and in leav...
<p>(A) The phenotypes of WT and four leaf coloration mutants grown with or without sucrose. (B) qRT-...
<p><b>(a)</b> Expression of the genes for NAD(H)-GDH (<i>LjGdh1</i>, <i>LjGdh2</i> and <i>LjGdh3</i>...
<p>Total RNA was extracted from 10-day-old WT and <i>atl31–1/atl6–1</i> plants grown under LL and ML...
<p>Expression of <i>SDP1</i>, <i>CTS</i>, <i>LACS6</i>, <i>LACS7</i>, <i>ACX1</i>, <i>ACX2</i>, <i>M...
<p>(a) PCR of genomic DNA showed the successful generation of the T-DNA insertion mutant. (b) RT-PCR...
<p>Transcript levels of these genes in transgenic plants are indicated relative to the level of WT p...
<p>Most transcripts increase less than 2-fold between LP1&2 and LP3&4 in Col, and increase 2-fold or...
<p>The qRT-PCR analysis of the expressions of two enzyme-encoding genes in chl degradation pathway (...
Real-time quantitative polymerase chain reaction (qPCR) has become widely used as a method to compar...
Gene expression of PLAT1 in WT roots (A) and leaves (B) was determined between one day and 14 days o...