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P53-M Real-Time PCR Array for Multi-Gene Expression Profiling and Microarray Data Validation: RT2 Profiler PCR Array

机译:用于多基因表达谱分析和微阵列数据验证的P53-M实时PCR阵列:RT2 Profiler PCR阵列

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摘要

Quantitative real-time reverse-transcription PCR (RT-qPCR) is presently the method of choice for validating gene expression results from high-density microarrays. However, the low throughput of traditional gene-by-gene RT-qPCR makes this process labor intensive and time consuming. To accelerate this laborious task, the SuperArray RT²Profiler PCR Array combines SYBR Green–based real-time RT-qPCR technology with a multi-gene array plate format to simultaneously analyze a panel of genes related to a specific disease or biological pathway.Each assay on the PCR array plate has been experimentally validated to insure gene-specific amplification. The reliability and reproducibility of the RT²Profiler PCR Array have been demonstrated by DNA sequencing and intra/inter-laboratory reproducibility comparisons. The DNA sequencing demonstrated 100% of the PCR products amplified from the correct target genes. In one laboratory, individual PCR assays produced a standard deviation of 0.24 cycles and a coefficient of variance of 0.92% in technical replicates. The correlation coefficient for Ct values between replicate runs was 0.997 and for fold changes (ΔΔCt) across thermocyclers was 0.976. Comparisons between two different laboratories using different thermocyclers showed correlation coefficients of 0.972 and 0.976 for ΔCt and ΔΔCt, respectively. Each PCR array also includes stringent controls to monitor RNA quality by assessing reverse transcription efficiency and genomic DNA contamination to ensure the reliability of the PCR array data.A practical application for the PCR array was demonstrated by identifying human pancreatic tumor–associated genes using the Cancer PathwayFinder RT²Profiler PCR Array. Results showed 23 genes exhibiting a statistically significant threefold or greater change in expression between a human pancreatic tumor and normal pancreas, including many genes previously linked to pancreatic cancer. Hence, the RT2 Profiler PCR Array system offers a simple, reliable, and convenient tool for multi-gene profiling and microarray data validation.
机译:实时定量逆转录PCR(RT-qPCR)是目前验证高密度微阵列基因表达结果的首选方法。但是,传统的逐个基因RT-qPCR的低通量使该过程费时费力。为了加快这项艰巨的任务,SuperArrayRT²ProfilerPCR Array结合了基于SYBR Green的实时RT-qPCR技术和多基因阵列板格式,可以同时分析与特定疾病或生物学途径相关的一组基因。 PCR阵列板已通过实验验证,可确保基因特异性扩增。 DNA测序和实验室内部/实验室间的可重复性比较证明了RT²ProfilerPCR阵列的可靠性和可重复性。 DNA测序证明100%的PCR产物均从正确的靶基因扩增而来。在一个实验室中,单独的PCR分析在技术重复中产生的标准偏差为0.24个循环,变异系数为0.92%。重复运行之间Ct值的相关系数为0.997,而热循环仪中倍数变化的相关系数(ΔΔCt)为0.976。在两个使用不同热循环仪的不同实验室之间进行的比较显示,ΔCt和ΔΔCt的相关系数分别为0.972和0.976。每个PCR阵列还包括严格的对照,通过评估逆转录效率和基因组DNA污染来监控RNA的质量,以确保PCR阵列数据的可靠性。PCR阵列的实际应用通过使用癌症鉴定人胰腺肿瘤相关基因得到了证明。 PathwayFinderRT²ProfilerPCR阵列。结果显示,在人类胰腺肿瘤和正常胰腺之间,有23个基因在表达上具有统计学上显着的三倍或更大的变化,其中包括许多先前与胰腺癌有关的基因。因此,RT 2 Profiler PCR Array系统为多基因分析和微阵列数据验证提供了一个简单,可靠和方便的工具。

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