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Detection of nucleic acids by fluorescence quenching

机译:通过荧光猝灭检测核酸

摘要

Single-stranded signal primers are modified by linkage to two dyes which form a donor/acceptor dye pair. The two dyes are positioned in sufficiently close spatial proximity on the signal primer that the fluorescence of the first dye is quenched by the second dye. The signal primer may further comprise a restriction endonuclease recognition site (RERS) between the two dyes. As the signal primer is initially single-stranded and remains single-stranded in the absence of target, the restriction endonuclease recognition site is not cleavable or nickable by the restriction endonuclease. In the presence of target, however, signal primer and the restriction endonuclease recognition site are rendered double-stranded and cleavable or nickable by the restriction endonuclease. Cleavage or nicking separates the two dyes and a change in fluorescence due to decreased quenching is detected as an indication of the presence of the target sequence or of target sequence amplification. IMAGE
机译:单链信号引物通过与形成供体/受体染料对的两种染料连接而被修饰。两种染料在信号引物上的位置足够接近,从而使第一种染料的荧光被第二种染料淬灭。信号引物可进一步在两种染料之间包含限制性核酸内切酶识别位点(RERS)。由于信号引物最初是单链的,在不存在靶标的情况下仍保持单链,因此限制性核酸内切酶识别位点不能被限制性核酸内切酶切割或切割。但是,在存在靶标的情况下,限制性内切核酸酶使信号引物和限制性内切核酸酶识别位点成为双链且可切割或可切割。切割或刻痕将两种染料分开,并且检测到由于淬灭减少而引起的荧光变化,这表明存在靶序列或靶序列扩增。 <图像>

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