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注意:在对 MIDTAL(用于检测有毒藻类的微阵列)进行现场验证之前,已采取措施优化探针特异性和信号强度。

Note: steps taken to optimise probe specificity and signal intensity prior to field validation of the MIDTAL (Microarray for the Detection of Toxic Algae).

机构信息

Marine Biological Association of the UK, The Laboratory, Plymouth, PL1 2 PB, UK,

出版信息

Environ Sci Pollut Res Int. 2013 Oct;20(10):6686-9. doi: 10.1007/s11356-012-1450-7. Epub 2013 May 2.

Abstract

A microarray for the detection of toxic algal species was developed in the European Union 7th Framework project MIDTAL. We initially tested all available fluorescence in situ hybridisation probes for toxic algae, which are normally designed to a length of 18 nt, and found that in most cases the signal was rather weak or all probes designed from the second half of the molecule were inaccessible in a microarray format because of secondary structure of the ribosomal RNA molecule We modified the length of the probes, the fragmentation of the rRNA, the stringency of the washing buffers and the length of the spacer molecules linking the probes to the glass surface of the microarray. Because of the secondary structure of the rRNA molecule, regions of the molecule can be difficult to access by the probes. Each of these modifications has improved probe accessibility and probe specificity to reduce false positives.

摘要

欧盟第七框架项目 MIDTAL 开发了一种用于检测有毒藻类物种的微阵列。我们最初测试了所有可用于有毒藻类的荧光原位杂交探针,这些探针通常设计为 18 个核苷酸长,但发现大多数情况下信号较弱,或者由于核糖体 RNA 分子的二级结构,所有设计自分子后半部分的探针都无法在微阵列格式中使用。我们修改了探针的长度、rRNA 的片段化、洗涤缓冲液的严格程度以及连接探针与微阵列玻璃表面的间隔分子的长度。由于 rRNA 分子的二级结构,分子的某些区域可能难以被探针接触。这些修改中的每一个都提高了探针的可及性和探针的特异性,以减少假阳性。

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