THE USE OF EUROPIUM (EU-3+) LABELED PRIMERS IN PCR AMPLIFICATION OF SPECIFIC TARGET DNA

被引:23
作者
DAHLEN, P [1 ]
IITIA, A [1 ]
MUKKALA, VM [1 ]
HURSKAINEN, P [1 ]
KWIATKOWSKI, M [1 ]
机构
[1] WALLAC OY,SF-20101 TURKU,FINLAND
关键词
TIME-RESOLVED FLUOROMETRY; EUROPIUM; POLYMERASE CHAIN REACTION (PCR); LABELED PRIMERS; NESTED PRIMERS; HIV-1;
D O I
10.1016/0890-8508(91)90009-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The polymerase chain reaction (PCR) has many potential applications in the field of DNA probe diagnostics. Here we describe a method that utilizes PCR and time-resolved fluorometry (TRF) for the detection of specific target DNA. First the DNA segment to be detected is amplified according to standard procedures. Then a pair of europium (Eu3+) and biotin-labelled primers nested within the amplified fragment is incorporated in a few additional PCR cycles. Thus amplified DNA fragments are generated that contain an affinity label (biotin) and a detectable label (europium). The doubly-labelled amplified DNA fragments are collected onto streptavidin coated microtitration strips and the bound Eu3+ is measured in a time-resolved fluorometer. We show here the application of this method to the detection of HIV-1 DNA. As few as five copies of HIV-1 DNA could readily be detected using this assay. The method described here is sensitive, rapid and easy to employ. In addition it lends itself to automation. © 1991.
引用
收藏
页码:143 / 149
页数:7
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