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Primer-Induced Labeling of Pea and Field Bean Chromosomes In Situ and In Suspension

机译:引物诱导的豌豆和大田豆染色体的原位和悬浮标记

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摘要

A protocol for primed in situ DNA labeling (PRINS) was optimized for pea (Pisum sativum L.) and field bean (Viola faba L.) chromosomes attached to coverslips Cloned DNA or synthetic oli-gonucleotides were used as probes for repetitive DNA sequences (rDNA, Fok-ele-ment) and different reaction conditions were tested to achieve the highest specific signal-to-background ratio. A procedure based on direct labeling by fluorescein-dUTP was compared with an indirect one using digoxigenin detected by fluores-cently labeled antibody. Under optimal conditions, strong and specific signals were obtained exclusively on chromosome regions known to contain respective DNA sequences. Compared to the direct labeling, significantly stronger signals were obtained when the indirect procedure was used. Both types of labeling were successfully applied to chromosomes in suspension and were shown to produce signals comparable to that obtained with chromosomes attached to coverslips It is expected that primed in situ DNA labeling en suspension (PRINSES) will provide a basis for flow-cytometric discrimination and sorting of otherwise indistinguishable chromosomes according to their specific fluorescent labeling.
机译:优化了豌豆(Pisum sativum L.)和田豆(Viola faba L.)染色体上附着有盖玻片的引发DNA原位标记的方案(PRINS)。克隆的DNA或合成的寡核苷酸被用作重复DNA序列的探针(测试了rDNA,Fok元件)和不同的反应条件,以实现最高的特定信噪比。使用荧光素标记的抗体检测的洋地黄毒苷,将基于荧光素-dUTP直接标记的方法与使用洋地黄毒苷的间接方法进行了比较。在最佳条件下,仅在已知包含各自DNA序列的染色体区域上获得强而特异性的信号。与直接标记相比,使用间接程序可获得明显更强的信号。两种类型的标记均已成功应用于悬浮染色体,并显示出与盖玻片上附着的染色体可比的信号。预期原位DNA悬浮标记(PRINSES)将为流式细胞仪识别和鉴定奠定基础。根据其特定的荧光标记对其他无法区分的染色体进行排序。

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