Detection technique of asymmetric RT-PCR-based amplified single-stranded DNA and its application to biosensor for detection of mRNA for cyanobacteria, Anabaena variabilis

被引:3
作者
Asai, R
Nakamura, C
Ikebukuro, K
Karube, I
Miyake, J
机构
[1] Natl Inst Ind Sci & Technol, Tissue Engn Res Ctr, Tsukuba, Ibaragi 3058562, Japan
[2] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
关键词
Anabaena variabilis; asymmetric PCR; mRNA; RT-PCR; surface plasmon resonance;
D O I
10.1023/A:1020609702434
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A real-time detection technique for mRNA was developed using a specific DNA probe. The design of the probe was based on a sequence polymorphism within the expressed mRNA of Anabaena variabilis PCC7120 by using the BIAcore 2000 biosensor, which uses surface plasmon resonance (SPR). The reverse transcription polymerase chain reaction (RT-PCR)-amplified single-stranded DNA (ssDNA), specific for ribonuclease P RNA B (rnpB) from A. variabilis, was determined by an SPR biosensor. Through these detection methods, the ssDNA amplified from rnpB could be detected within 10 min after asymmetric RT-PCR.
引用
收藏
页码:1677 / 1682
页数:6
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