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Evaluation of locked nucleic acids for signal enhancement of oligonucleotide probes for microalgae immobilised on solid surfaces

机译:锁定核酸的评估,以增强寡核苷酸探针固定在固体表面上的微藻信号

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摘要

Biosensors and microarrays are powerful tools for species detection and monitoring of microorganisms. A reliable identification of microorganisms with probe-based methods requires highly specific and sensitive probes. The introduction of locked nucleic acid (LNA) promises an enhancement of specificity and sensitivity of molecular probes. In this study, we compared specificity and sensitivity of conventional probes and LNA modified probes in two different solid phase hybridisation methods: sandwich hybridisation on biosensors and on DNA microarrays. In combination with DNA-microarrays, the LNA probes displayed an enhancement of sensitivity, but also gave more false-positive signals. With the biosensor, the LNA probes showed neither signal enhancement nor discrimination of a single mismatch. In all cases, conventional DNA probes showed equal or better results than LNA probes. In conclusion, LNA technology may have great potential in methods that use probes in suspension and in gene expressions studies, but under certain solid surface-hybridisation applications, they do not improve signal intensity.
机译:生物传感器和微阵列是用于物种检测和监测微生物的强大工具。使用基于探针的方法可靠地鉴定微生物需要高度特异性和灵敏的探针。锁定核酸(LNA)的引入有望增强分子探针的特异性和敏感性。在这项研究中,我们在两种不同的固相杂交方法中比较了常规探针和LNA修饰探针的特异性和敏感性:在生物传感器和DNA微阵列上的夹心杂交。与DNA微阵列结合使用时,LNA探针显示出更高的灵敏度,但也给出了更多的假阳性信号。使用生物传感器时,LNA探针既未显示信号增强,也未显示单个错配。在所有情况下,常规的DNA探针显示出与LNA探针相同或更好的结果。总之,LNA技术在悬浮中使用探针的方法和基因表达研究中可能具有巨大潜力,但在某些固体表面杂交应用中,它们不能改善信号强度。

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