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A modified method to isolate genomic DNA from plants without liquid nitrogen.

机译:一种从没有液氮的植物中分离基因组DNA的改良方法。

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This paper presents a quick, simple and cheap procedure to isolate DNA from plants, which involves alternate cold (-80 degrees C) and heat shock (60 degrees C) treatments in order to break down the cell wall without using liquid N2. Samples of young, tender, leaves of some plants species (including Desmodium giganticum, Aegle marmelos, Solanum xanthocarpum, Solanum indicum, Tribulus terrestris, Oroxylum indicum, Boerhavia diffusa, Trianthema portulacastrum, Trianthema monogyna and Datura innoxia [D. metel]), collected from the Botanical Garden of Panjab University, Chandigarh, and various other nurseries in India, were used. In conclusion, this method can be used for extraction of DNA of high-quality and high yield from any type of plant tissue and is suitable for all types of molecular biology experiments. The extracted DNA was stable and gave the same results in PCR, microsatellite fingerprinting, PCR-restriction fragment length polymorphism and random amplified polymorphic DNA after 2 years of storage at 4 degrees C.
机译:本文提出了一种快速,简单且廉价的从植物中分离DNA的方法,该方法包括交替进行冷(-80摄氏度)和热休克(60摄氏度)处理,以在不使用液体N 的情况下分解细胞壁。 2 。某些植物物种的幼嫩叶子的样品(包括 Desmodium giganticum,Aegle marmelos,Solanum xanthocarpum,Solanum indicum,Tribulus terrestris,Oroxylum indicum,Boerhavia diffusa,Trianthema portulacastrum,Trianthema monogyna 和使用了从印度昌迪加尔的潘加卜大学植物园和印度其他各种苗圃中收集的曼陀罗(Datura innoxia)[])。总之,该方法可用于从任何类型的植物组织中提取高质量,高产量的DNA,适用于所有类型的分子生物学实验。提取的DNA稳定,在4°C下保存2年后,在PCR,微卫星指纹图谱,PCR限制性片段长度多态性和随机扩增的多态性DNA中具有相同的结果。

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