AbstractReal-time reverse transcription polymerase chain reaction (RT-PCR) is regarded as one of the most useful and powerful tools for characterizing hematopoietic stem cells (HSCs), because samples of extremely small cell numbers can be analyzed. The expression levels determined by RT-PCR are based on relative quantification; therefore, the selection of an appropriate reference gene with a relatively stable expression level under most conditions is crucial. Here, we determined that beta2-microglobulin (B2m) is an appropriate reference gene for analyzing mouse HSCs by a novel method using single-cell RT-PCR. Clonally sorted HSCs were subjected to RT reactions with exogenous RNA fragments and then to real-time PCR. Next, the relative gene e...
Item does not contain fulltextOBJECTIVE: Quantitative assessment of gene expression in stem cells is...
Up to now quantitative PCR based assay is the most common method for characterizing or confirming ge...
<div><p>The purpose of this study was to perform a comprehensive evaluation and selection of referen...
Real-time reverse transcription polymerase chain reaction (RT-PCR) is regarded as one of the most us...
博士(医学) 乙第2943号(主論文の要旨、要約、審査結果の要旨、本文),著者名:Yu MATSUZAKI・Terumasa UMEMOTO・Yuji TANAKA・Teruo OKANO・Masay...
Background: Selecting stably expressed reference genes is essential for proper reverse transcription...
Introduction: Real time RT-PCR is a widely used technique to evaluate and confirm gene expression da...
Background The choice of reliable reference genes is a prerequisite for valid results when analyzin...
We report here a systematic, quantitative population analysis of transcription factor expression wit...
Background: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
BACKGROUND: Polymerase Chain Reaction (PCR) has become an important diagnostic and research tool of ...
BACKGROUND: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
Up to now quantitative PCR based assay is the most common method for characterizing or confirming ge...
<div><p>Background</p><p>Quantitative real time polymerase chain reaction (qPCR) is an extremely pow...
Background: Reference genes, which are often referred to housekeeping genes, are fr...
Item does not contain fulltextOBJECTIVE: Quantitative assessment of gene expression in stem cells is...
Up to now quantitative PCR based assay is the most common method for characterizing or confirming ge...
<div><p>The purpose of this study was to perform a comprehensive evaluation and selection of referen...
Real-time reverse transcription polymerase chain reaction (RT-PCR) is regarded as one of the most us...
博士(医学) 乙第2943号(主論文の要旨、要約、審査結果の要旨、本文),著者名:Yu MATSUZAKI・Terumasa UMEMOTO・Yuji TANAKA・Teruo OKANO・Masay...
Background: Selecting stably expressed reference genes is essential for proper reverse transcription...
Introduction: Real time RT-PCR is a widely used technique to evaluate and confirm gene expression da...
Background The choice of reliable reference genes is a prerequisite for valid results when analyzin...
We report here a systematic, quantitative population analysis of transcription factor expression wit...
Background: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
BACKGROUND: Polymerase Chain Reaction (PCR) has become an important diagnostic and research tool of ...
BACKGROUND: Quantitative real time polymerase chain reaction (qPCR) is an extremely powerful techniq...
Up to now quantitative PCR based assay is the most common method for characterizing or confirming ge...
<div><p>Background</p><p>Quantitative real time polymerase chain reaction (qPCR) is an extremely pow...
Background: Reference genes, which are often referred to housekeeping genes, are fr...
Item does not contain fulltextOBJECTIVE: Quantitative assessment of gene expression in stem cells is...
Up to now quantitative PCR based assay is the most common method for characterizing or confirming ge...
<div><p>The purpose of this study was to perform a comprehensive evaluation and selection of referen...