2006China Medical EngineeringRequires access

A modified alkaline lysis method for extraction of plasmid DNA

Liu Yong-he

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Abstract

[Objective] Introduce a method for rapid extraction of Superior-Quality Plasmid DNA. [Method] Use alternative reagent to establish modified alkaline lysis method for extraction of plasmid DNA and use agarose electrophoresis to examine the quality of plasmid DNA, ultraviolet spectrophotometry to evaluate its production and purity, restricted enzyme cutting to examine its availability. [Results] The agarose electrophoresis showed that the plasmid DNA band was bright, mainly by form of superhelix. A260/280 was 1.903, DNA concentration was 320μg/ml, and we got 500 bp target fragment by restricted enzyme cutting. [Conclusion] We can get high purity of sample DNA by this simple and practical new method , it can meet the requirement of routine molecular biochemistry experiments.

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[Objective] Introduce a method for rapid extraction of Superior-Quality Plasmid DNA. [Method] Use alternative reagent to establish modified alkaline lysis method for extraction of plasmid DNA and use agarose electrophoresis to examine the quality of plasmid DNA, ultraviolet spectrophotometry to evaluate its production and purity, restricted enzyme cutting to examine its availability. [Results] The agarose electrophoresis showed that the plasmid DNA band was bright, mainly by form of superhelix. A260/280 was 1.903, DNA concentration was 320μg/ml, and we got 500 bp target fragment by restricted enzyme cutting. [Conclusion] We can get high purity of sample DNA by this simple and practical new method , it can meet the requirement of routine molecular biochemistry experiments.

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Available abstract

[Objective] Introduce a method for rapid extraction of Superior-Quality Plasmid DNA. [Method] Use alternative reagent to establish modified alkaline lysis method for extraction of plasmid DNA and use agarose electrophoresis to examine the quality of plasmid DNA, ultraviolet spectrophotometry to evaluate its production and purity, restricted enzyme cutting to examine its availability. [Results] The agarose electrophoresis showed that the plasmid DNA band was bright, mainly by form of superhelix. A260/280 was 1.903, DNA concentration was 320μg/ml, and we got 500 bp target fragment by restricted enzyme cutting. [Conclusion] We can get high purity of sample DNA by this simple and practical new method , it can meet the requirement of routine molecular biochemistry experiments.

Key concepts: Alkaline lysis, Plasmid preparation, Plasmid, Lysis, DNA, Agarose gel electrophoresis, Agarose, DNA extraction

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