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- 2025年07月08日
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文献和实验Preparation of Bacteriophage Lysates and Pure DNA
Preparation of pure bacteriophage DNA used to rely on using CsCl gradients to give high purity or methods that yielded DNA that was either of low recovery or subject to significant genomic contamination. Recently though, new methods have come
We report a simple homogeneous fluorescence assay for quantification of DNA polymerase function in high throughput. The fluorescence signal is generated by the DNA polymerase triggering opening of a molecular beacon extension of the template
Kingfisher Flex 96 Plant DNA High Pure Protocol
Solution and 500ul Lysis Buffer to the sample. 7. Set up KingFisher Flex instrument by press “tart Key”on the Mag Bind Plant DNA Protocol and load plates according to prompts from Kingfisher Unit. 8. After the DNA isolation, seal Elution Plate
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