<p>Quantitative PCR for (A) <i>gli1</i>, (B) <i>ptch1</i>, and (C) <i>hsd11b1</i> was performed on Hh ligand treated and Hedgehog ligand and SFE co-treated TRAMPC2 cells. Transcripts concentrations were normalized to control. * indicates p<0.05. In the lower figure, transcripts concentrations of (A) <i>gli1</i>, (B) <i>ptch1</i>, and (C) <i>hsd11b1</i> are represented by quantified sequencing reads, in the form of counts-per-million-reads.</p
Aim: Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is still the “gold stand...
<p>Correlation of RNASeq and qPCR relative expression of selected genes for early (A) and late-expon...
<p>(Top row) Normalized read counts from RNA-seq analysis. (Middle row) RT-qPCR validation using tis...
GLI1, PTCH1, and reference gene CT (cycle threshold) for ARPE-19, HEK293T, hTERT RPE-1, and NIH/3T3 ...
<p>The expression profiles of 10 UP and 10 DOWN contigs (randomly selected) were analysed by qPCR to...
<p>Top, Representative immunoblots of each protein and GAPDH, as a loading control. Bottom, Bar grap...
<p>Total RNA from A549, AG04450 and HeLa cells was probed by qPCR using primers specific for circula...
<p>MDMs were stimulated with TLR2/1L (black bars) or IFN-γ (gray bars) for 2, 6, and 24 hours and <b...
<p>Validation of changes in mRNA expression by quantitative real-time RT-PCR (qRT-PCR) for genes rep...
<p>Validation of 12 randomly chosen, differentially expressed genes was performed with qPCR using th...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
BACKGROUND: Polymerase Chain Reaction (PCR) has become an important diagnostic and research tool of ...
<p>Twenty-eight differentially expressed genes, according to array analysis, were tested by qPCR in ...
<p>RNA was harvested from hAT2 cells cultured on collagen or Matrigel at 12 = 2. The relative expres...
<p>QPCR verification result of 14 selected genes. The mRNA expression levels of these genes were nor...
Aim: Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is still the “gold stand...
<p>Correlation of RNASeq and qPCR relative expression of selected genes for early (A) and late-expon...
<p>(Top row) Normalized read counts from RNA-seq analysis. (Middle row) RT-qPCR validation using tis...
GLI1, PTCH1, and reference gene CT (cycle threshold) for ARPE-19, HEK293T, hTERT RPE-1, and NIH/3T3 ...
<p>The expression profiles of 10 UP and 10 DOWN contigs (randomly selected) were analysed by qPCR to...
<p>Top, Representative immunoblots of each protein and GAPDH, as a loading control. Bottom, Bar grap...
<p>Total RNA from A549, AG04450 and HeLa cells was probed by qPCR using primers specific for circula...
<p>MDMs were stimulated with TLR2/1L (black bars) or IFN-γ (gray bars) for 2, 6, and 24 hours and <b...
<p>Validation of changes in mRNA expression by quantitative real-time RT-PCR (qRT-PCR) for genes rep...
<p>Validation of 12 randomly chosen, differentially expressed genes was performed with qPCR using th...
Five genes were selected to verify RNA-Seq results using qRT-PCR. Graphs on the left (A, C, E, G, I,...
BACKGROUND: Polymerase Chain Reaction (PCR) has become an important diagnostic and research tool of ...
<p>Twenty-eight differentially expressed genes, according to array analysis, were tested by qPCR in ...
<p>RNA was harvested from hAT2 cells cultured on collagen or Matrigel at 12 = 2. The relative expres...
<p>QPCR verification result of 14 selected genes. The mRNA expression levels of these genes were nor...
Aim: Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) is still the “gold stand...
<p>Correlation of RNASeq and qPCR relative expression of selected genes for early (A) and late-expon...
<p>(Top row) Normalized read counts from RNA-seq analysis. (Middle row) RT-qPCR validation using tis...