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qPCRTag分析 - 高通量,实时定量PCR检测方法的基因分型Sc2.0
JoVE 신문
생물학
This content is Free Access.
JoVE 신문 생물학
qPCRTag Analysis – A High Throughput, Real Time PCR Assay for Sc2.0 Genotyping
DOI:

07:00 min

May 25, 2015

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Chapters

  • 00:05Title
  • 01:34Prepare Yeast Genomic DNA
  • 03:15Prepare and Disperse qPCR Master Mix Template DNA and Primers
  • 05:05Real Time PCR and Data Analysis
  • 05:50Results: qPCR Results with WT and Synthetic Yeast gDNA and Primers
  • 06:39Conclusion

Summary

자동 번역

Designer chromosomes of the Synthetic Yeast Genome project, Sc2.0, can be distinguished from their native counterparts using a PCR-based genotyping assay called PCRTagging, which has a presence/absence endpoint. Here we describe a high-throughput real time PCR detection method for PCRTag genotyping.

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