<p>Similar to RT-PCR analysis, the same cDNA of the respective human bone marrow-derived multipotent stromal cell (BM-MSC) line (biological triplicates, n = 3) synthesized by standard reverse transcription (RT samples) and Whole Transcriptome Amplification (WTA samples) was used for qPCR analysis. (A-C) The WTA samples revealed a significantly decreased expression level of the medium-copy <i>HOX</i> genes like <i>HOXA9</i>, <i>HOXB7</i> and <i>HOXD8</i> in comparison to RT samples. (D) The reference gene <i>RPL13A</i> is expressed on a significantly higher level compared to the <i>HOX</i> genes resulting in no significantly different qPCR results after WTA.</p
BACKGROUND: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful technique for monit...
Reverse transcription quantitative polymerase chain reaction (RT-qPCR) enables the monitoring of cha...
<p>Similar to RT-PCR analysis, the same cDNA of the respective human bone marrow-derived multipotent...
<div><p>The amplification of RNA is becoming increasingly important, as often only limited amounts o...
The amplification of RNA is becoming increasingly important, as often only limited amounts of cells ...
The amplification of RNA is becoming increasingly important, as often only limited amounts of cells ...
<p>In this experiment, the same RNA of the respective human bone marrow-derived multipotent stromal ...
<p>When cDNA was synthesized by standard cDNA synthesis, the tested medium- and low-copy <i>HOX</i> ...
<p>The same cDNA from human bone marrow-derived multipotent stromal cell (BM-MSC) line 1 and 3 was c...
<p>The expression level of seven medium-, and low copy <i>HOX</i> transcripts is documented for biol...
<p>Human bone marrow-derived multipotent stromal cell (BM-MSC) lines were cultivated and expanded un...
Background: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
In the next-generation sequencing era, RT-qPCR is still widely employed to quantify levels of nuclei...
Quantitative real-time reverse-transcription polymerase chain reaction (RT-qPCR) remains the most se...
BACKGROUND: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful technique for monit...
Reverse transcription quantitative polymerase chain reaction (RT-qPCR) enables the monitoring of cha...
<p>Similar to RT-PCR analysis, the same cDNA of the respective human bone marrow-derived multipotent...
<div><p>The amplification of RNA is becoming increasingly important, as often only limited amounts o...
The amplification of RNA is becoming increasingly important, as often only limited amounts of cells ...
The amplification of RNA is becoming increasingly important, as often only limited amounts of cells ...
<p>In this experiment, the same RNA of the respective human bone marrow-derived multipotent stromal ...
<p>When cDNA was synthesized by standard cDNA synthesis, the tested medium- and low-copy <i>HOX</i> ...
<p>The same cDNA from human bone marrow-derived multipotent stromal cell (BM-MSC) line 1 and 3 was c...
<p>The expression level of seven medium-, and low copy <i>HOX</i> transcripts is documented for biol...
<p>Human bone marrow-derived multipotent stromal cell (BM-MSC) lines were cultivated and expanded un...
Background: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
In the next-generation sequencing era, RT-qPCR is still widely employed to quantify levels of nuclei...
Quantitative real-time reverse-transcription polymerase chain reaction (RT-qPCR) remains the most se...
BACKGROUND: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful technique for monit...
Reverse transcription quantitative polymerase chain reaction (RT-qPCR) enables the monitoring of cha...