<p>U-II is expressed as mRNA in HCC samples. Human tumoural cells SW-13 were used as positive control. Data were normalized on the basis of GAPDH and expressed as mean ± standard error of the mean (SEM) of three different human specimens.</p
<p>(A) Data of differentiated MenSCs and BMSCs were normalized to corresponding GAPDH and calculated...
<p>(<b>A</b>) To confirm the specificity of the HBA1 and HBB primers for qRT-PCR, expression of HBA1...
<p>qRT-PCR was performed on cell lysates from a range of UBC cell lines and the control SV-40 immort...
BACKGROUND: Polymerase Chain Reaction (PCR) has become an important diagnostic and research tool of ...
Variability of clinical samples with respect to cell types and quality makes it indispensable to nor...
<p>GAPDH was used as an internal control gene. Final abundance figures were adjusted to yield an arb...
<p>(A) QRT-PCR analysis of mRNA form human hepatic stellate cell line (LX-2) and human hepatocellula...
<div><p>Reference genes (RG) as sample internal controls for gene transcript level analyses by quant...
<p>Values are expressed as relative gene expression versus GAPDH and represent the mean ±SD of three...
<p>Expression of genes encoding nuclear receptors (A), phase I enzymes (B), phase II enzymes (C), an...
<p>(A) <i>RTL1</i> expression in human HCC and matched benign liver samples was analyzed by RT-PCR. ...
<p>The mRNA levels of selected genes were evaluated in all treated cells and compared to control. Da...
<p>(A) Relative mRNA expression levels of GPR87 and CD133 were determined by quantitative polymerase...
<p>The three HCC patients whose specimens were studied by RNA-Seq were male, aged from 55–61. All we...
<p>Total RNA from these cell lines was subjected toRT-PCR using primers specific for human <i>FCGRT<...
<p>(A) Data of differentiated MenSCs and BMSCs were normalized to corresponding GAPDH and calculated...
<p>(<b>A</b>) To confirm the specificity of the HBA1 and HBB primers for qRT-PCR, expression of HBA1...
<p>qRT-PCR was performed on cell lysates from a range of UBC cell lines and the control SV-40 immort...
BACKGROUND: Polymerase Chain Reaction (PCR) has become an important diagnostic and research tool of ...
Variability of clinical samples with respect to cell types and quality makes it indispensable to nor...
<p>GAPDH was used as an internal control gene. Final abundance figures were adjusted to yield an arb...
<p>(A) QRT-PCR analysis of mRNA form human hepatic stellate cell line (LX-2) and human hepatocellula...
<div><p>Reference genes (RG) as sample internal controls for gene transcript level analyses by quant...
<p>Values are expressed as relative gene expression versus GAPDH and represent the mean ±SD of three...
<p>Expression of genes encoding nuclear receptors (A), phase I enzymes (B), phase II enzymes (C), an...
<p>(A) <i>RTL1</i> expression in human HCC and matched benign liver samples was analyzed by RT-PCR. ...
<p>The mRNA levels of selected genes were evaluated in all treated cells and compared to control. Da...
<p>(A) Relative mRNA expression levels of GPR87 and CD133 were determined by quantitative polymerase...
<p>The three HCC patients whose specimens were studied by RNA-Seq were male, aged from 55–61. All we...
<p>Total RNA from these cell lines was subjected toRT-PCR using primers specific for human <i>FCGRT<...
<p>(A) Data of differentiated MenSCs and BMSCs were normalized to corresponding GAPDH and calculated...
<p>(<b>A</b>) To confirm the specificity of the HBA1 and HBB primers for qRT-PCR, expression of HBA1...
<p>qRT-PCR was performed on cell lysates from a range of UBC cell lines and the control SV-40 immort...