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A microarray scanner for the real-time quantitative detection

机译:用于实时定量检测的微阵列扫描仪

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摘要

The real-time and quantitative detection assay is important for the gene detection. With the TaqMan probes for the detection based polymerase chain reaction (PCR), four targets could be checked in a single process in solution assay. A new method is developed to immobilize the TaqMan probes on a microarray, which could be used to the multi-target gene fragment quantitative detection with PCR. A new type microarray scanner is designed for the assay. A thermocycler system was built into the scanner platform. A new type of the vessel sealed with the gene amplification solution which could perform the thermo-cycling and scanning. To decrease the background intensity a confocal system was used as the fluorescent intensity detection in the scanner. To calculate the gene quantity, a standard liner graph was draw with the fluorescent intensity versus the cycles. From the standard liner, the quantity of the original gene fragment could be calculated in time with the cycles. This scanner offers the great advantage of real-time quantitative detection of DNA targets in a microarray.
机译:实时定量检测测定法对于基因检测很重要。使用用于基于检测的聚合酶链反应(PCR)的TaqMan探针,可以在溶液测定的单个过程中检查四个目标。开发了一种将TaqMan探针固定在微阵列上的新方法,该方法可用于PCR多目标基因片段的定量检测。一种新型的微阵列扫描仪被设计用于该测定。扫描仪平台内置了热循环仪系统。一种新型的用基因扩增溶液密封的容器,可以进行热循环和扫描。为了降低背景强度,使用共聚焦系统作为扫描仪中的荧光强度检测。为了计算基因数量,绘制标准衬里图,其中荧光强度相对于循环。从标准衬里,可以随周期及时计算出原始基因片段的数量。该扫描仪具有实时定量检测微阵列中DNA靶标的巨大优势。

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