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首页> 外文期刊>Sensors and Actuators. B, Chemical >A novel real-time PCR machine with a miniature spectrometer for fluorescence sensing in a micro liter volume glass capillary
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A novel real-time PCR machine with a miniature spectrometer for fluorescence sensing in a micro liter volume glass capillary

机译:新型带有微型光谱仪的实时PCR仪,用于在微升体积的玻璃毛细管中进行荧光传感

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This study sets up a prototype of real-time polymerase chain reaction (RT-PCR) machine that employs a miniature spectrometer for detecting the emission of fluorescence intensity from RT-PCR mix in a micro liter volume glass capillary. The RT-PCR machine is one of the major instruments for SARS virus test during the outbreak in Asia in early 2003. Comparing with traditional RT-PCR machine with discrete channels fluorescence wavelength detection, the prototype can provide continuous wavelength detection and can be employed for multiplex DNA quantification. However, only one HBV SC 11 DNA template with the SYBR Green I labeling dye were used in this study to compare DNA quantification accuracy and reproducibility of the present system and the commercial system. The two machines have different optical engine arrangement and so two separate analytical models were proposed to predict the fluorescence intensity from the RT-PCR mix during thermal cycling for the machines. Predicted results agree well with the measured data for both machines. From the predicted results, different approaches should be adopted to determine the initial DNA concentration for quantification from time recorded history of the fluorescence intensity. Measured results illustrate that the RT-PCR prototype has the same accuracy for DNA quantification and reproducibility within five intra-assay samples as compared with the commercial machine.
机译:这项研究建立了一个实时聚合酶链反应(RT-PCR)机器的原型,该机器采用了一种微型光谱仪来检测微升体积玻璃毛细管中RT-PCR混合物发出的荧光强度。 RT-PCR机是2003年初亚洲爆发期间用于SARS病毒测试的主要仪器之一。与具有离散通道荧光波长检测的传统RT-PCR机相比,该原型可以提供连续的波长检测,可用于多重DNA定量。但是,本研究仅使用一种带有SYBR Green I标记染料的HBV SC 11 DNA模板来比较本系统和商业系统的DNA定量准确性和可重复性。这两台机器具有不同的光学引擎布置,因此提出了两个单独的分析模型,以预测机器热循环过程中RT-PCR混合物的荧光强度。预测结果与两台机器的测量数据吻合得很好。根据预测结果,应采用不同的方法来确定初始DNA浓度,以便根据荧光强度的时间记录历史进行定量。测量结果表明,与商用仪器相比,RT-PCR原型在五个批内样品中的DNA定量和重现性具有相同的准确性。

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