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METHOD FOR DETERMINING BASE SEQUENCE OF PROBE NUCLEIC ACID BASED ON HIGHER-ORDER STRUCTURE, AND DNA MICROARRAY

机译:基于高阶结构和DNA微阵列的探针核酸碱基序列确定方法

摘要

PROBLEM TO BE SOLVED: To provide a method for designing an oligonucleotide having the heightened certainty of formation of a double-stranded chain, and heightened sequence specificity by considering the higher-order structure such as the secondary structure of a target gene, and a DNA microarray mounting the oligonucleotide as a probe; and to improve the sensitivity, the repeatability and the ability for identifying the target gene, of the DNA microarray.;SOLUTION: The probe is designed by predicting a stem region for forming the double-stranded chain by autocompensation properties, and a loop region of a single-stranded chain from the higher-order structure such as the secondary structure of the target gene sequence, and evaluating the sequence similarity at the vicinity of the loop region and an experimental condition to narrow down the region suitable for hybridization of the oligonucleotide. The sequence of the loop region shown in the figure is sometimes different in a family sequence of a mRNA, and can be identified. The hybridizing ability with the probe of a complementary sequence is high because of a single-stranded chain to enable the improvement of sensitivity and repeatability to be expected.;COPYRIGHT: (C)2006,JPO&NCIPI
机译:解决的问题:提供一种设计寡核苷酸的方法,该寡核苷酸通过考虑靶基因的二级结构等高级结构和DNA,来提高双链形成的确定性,并提高序列特异性。装有寡核苷酸作为探针的微阵列; ;解决方案:通过自动补偿特性预测形成双链链的茎区域和DNA的环状区域来设计探针。一条来自目标基因序列二级结构等高级结构的单链,并评估环区附近的序列相似性和实验条件,以缩小适合寡核苷酸杂交的区域。图中所示的环区域的序列有时在mRNA的家族序列中不同,并且可以被识别。由于具有单链链,因此与互补序列探针的杂交能力很高,从而有望提高灵敏度和可重复性。;版权所有:(C)2006,JPO&NCIPI

著录项

  • 公开/公告号JP2006051006A

    专利类型

  • 公开/公告日2006-02-23

    原文格式PDF

  • 申请/专利权人 DAINAKOMU:KK;

    申请/专利号JP20040260304

  • 申请日2004-08-11

  • 分类号C12Q1/68;C12M1/00;G01N33/53;G01N37/00;C12N15/09;

  • 国家 JP

  • 入库时间 2022-08-21 21:53:41

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