For reliable results from quantitative RT-PCR, the starting quantity of total RNA and other parameters need to be controlled. Most studies do this by normalising their results to a single reference gene. This study quantified the mRNA expression of three putative reference genes (ubiquitin C, cyclophilin E, and porphobilinogen deaminase) and the target gene hepatocyte growth factor receptor (HGFR) in matched colorectal tumour and normal mucosa samples. Each of the putative reference genes was found to be significantly over-expressed in the tumour samples compared to the normal samples. When HGFR expression was normalised to each of these reference genes using the 2 (-DeltaDeltaC(T)) method of relative quantification, the number of tumour sa...
In this study, the expression level of two housekeeping genes, 18S ribosomal RNA and β-glucuronidase...
<div><p>Reference genes (RG) as sample internal controls for gene transcript level analyses by quant...
Reference genes (RG) as sample internal controls for gene transcript level analyses by quantitative ...
For interpretation of quantitative gene expression measurements in clinical tumor samples, a normali...
Contains fulltext : 47521.pdf (publisher's version ) (Closed access)For interpreta...
Background: Gene expression analysis has many applications in cancer diagnosis, prognosis and therap...
Background: Gene expression analysis has many applications in cancer diagnosis, prognosis and therap...
Quantitative real-time reverse-transcription polymerase chain reaction (RT-qPCR) remains the most se...
Abstract Background Housekeeping genes are routinely used as endogenous references to account for ex...
International audienceGene expression quantification using reverse transcription-quantitative polyme...
International audienceGene expression quantification using reverse transcription-quantitative polyme...
International audienceGene expression quantification using reverse transcription-quantitative polyme...
In quantitative reverse transcription–polymerase chain reaction (qRT–PCR), normalization using refer...
In quantitative reverse transcription–polymerase chain reaction (qRT–PCR), normalization using refer...
<div><p>Accurate normalization is a primary component of a reliable gene expression analysis based o...
In this study, the expression level of two housekeeping genes, 18S ribosomal RNA and β-glucuronidase...
<div><p>Reference genes (RG) as sample internal controls for gene transcript level analyses by quant...
Reference genes (RG) as sample internal controls for gene transcript level analyses by quantitative ...
For interpretation of quantitative gene expression measurements in clinical tumor samples, a normali...
Contains fulltext : 47521.pdf (publisher's version ) (Closed access)For interpreta...
Background: Gene expression analysis has many applications in cancer diagnosis, prognosis and therap...
Background: Gene expression analysis has many applications in cancer diagnosis, prognosis and therap...
Quantitative real-time reverse-transcription polymerase chain reaction (RT-qPCR) remains the most se...
Abstract Background Housekeeping genes are routinely used as endogenous references to account for ex...
International audienceGene expression quantification using reverse transcription-quantitative polyme...
International audienceGene expression quantification using reverse transcription-quantitative polyme...
International audienceGene expression quantification using reverse transcription-quantitative polyme...
In quantitative reverse transcription–polymerase chain reaction (qRT–PCR), normalization using refer...
In quantitative reverse transcription–polymerase chain reaction (qRT–PCR), normalization using refer...
<div><p>Accurate normalization is a primary component of a reliable gene expression analysis based o...
In this study, the expression level of two housekeeping genes, 18S ribosomal RNA and β-glucuronidase...
<div><p>Reference genes (RG) as sample internal controls for gene transcript level analyses by quant...
Reference genes (RG) as sample internal controls for gene transcript level analyses by quantitative ...