Universal and rapid salt-extraction of high quality genomic DNA for PCR-based techniques

被引:2271
作者
Aljanabi, SM [1 ]
Martinez, I [1 ]
机构
[1] NORWEGIAN INST FISHERIES & AQUACULTURE, TROMSO, NORWAY
关键词
D O I
10.1093/nar/25.22.4692
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A very simple, fast, universally applicable and reproducible method to extract high quality megabase genomic DNA from different organisms is decribed, We applied the same method to extract high quality complex genomic DNA from different tissues (wheat, barley, potato, beans, pear and almond leaves as well as fungi, insects and shrimps' fresh tissue) without any modification. The method does not require expensive and environmentally hazardous reagents and equipment, It can be performed even in low technology laboratories, The amount of tissue required by this method is similar to 50-100 mg, The quantity and the quality of the DNA extracted by this method is high enough to perform hundreds of PCR-based reactions and also to be used in other DNA manipulation techniques such as restriction digestion, Southern blot and cloning.
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页码:4692 / 4693
页数:2
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