新型非同位素赤霉素DNA探针标记及荧光检测系统

Y. Yamada, H. Sugiyama, N. Kagiyama, M. Momiyama, Y. Kondou
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引用次数: 0

摘要

利用赤霉素(GA4)建立了一种新的高灵敏度非同位素DNA标记和荧光快速检测系统。DNA被标记为GA4,通过8个原子连接间隔(GA4-[8]-dUTP)通过随机引物的方法连接到dUTP。将膜结合的靶DNA与ga4标记的探针杂交后,利用与碱性磷酸酶(ALP)结合的抗ga4 Fab片段,通过ELISA原理检测杂交产物。新的GA4系统使用一种新的荧光染料,2-羟基-3-萘酸-2'-苯基苯胺磷酸(HNPP)作为ALP的底物,可以在几个小时内在尼龙膜上的点印迹和southern印迹中检测到0.1 pg的同源DNA。新开发的GA4体系和HNPP荧光检测方法不仅具有高灵敏度和低本底的特点,而且在标记反应中GA4-dUTP与dUTP的比例很大的范围内,DNA检测的灵敏度是相同的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel nonisotopic gibberellin DNA probe labeling and fluorescent detection system
A novel highly sensitive nonisotopic DNA labeling with Gibberellin (GA4) and a new fluorescent fast detection system have been developed. The DNA is labeled with GA4 linked to dUTP via an 8 atom linker spacer (GA4-[8]-dUTP) by a random-primed method. Following hybridization of a membrane-bound target DNA with a GA4-labeled probe, the hybrids are detected by the ELISA principle using anti-GA4 Fab fragments conjugated to alkaline phosphatase (ALP). The novel GA4 system allows the detection of 0.1 pg homologous DNA within several hours in dot- and Southern-blots on nylon membranes using a new fluorochrome, 2-hydroxy-3-naphthoic-acid-2'-phenyl-anilide phosphate (HNPP), as the substrate for ALP. The newly developed GA4 system and HNPP fluorescent detection method exhibits not only high sensitivity and low background, but the sensitivity of DNA detection is identical over a wide range of ratio of GA4-dUTP to dUTP in labeling reaction.
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