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Related Concept Videos

Real Time RT-PCR02:57

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DNA isolation protocols can be fast and straightforward or complex and time-consuming depending on the type and quality of DNA required for further processing. For example, plasmid DNA extraction is a bit more complicated than genomic DNA extraction because of the need for an appropriate lysis method to separate plasmid DNA from gDNA during isolation. However, for specific applications, such as long-range DNA sequencing that require a good yield of high- quality DNA samples, we need to follow...
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Digital Polymerase Chain Reaction Assay for the Genetic Variation in a Sporadic Familial Adenomatous Polyposis Patient Using the Chip-in-a-tube Format
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[Digital PCR and its application in biological detection].

Xiu Jing Feng1, Hong Mei Yi1, Xing Xu Ren1

  • 1Beijing Key Laboratory of Maize DNA Fingerprinting and Molecular Breeding, Maize Research Center, Beijing Academy of Agricultural and Forestry Sciences, Beijing 100097, China.

Yi Chuan = Hereditas
|April 22, 2020
PubMed
Summary

Digital PCR (dPCR) offers sensitive and accurate nucleic acid quantification without standard curves. This review details dPCR technology, its applications in GMOs, disease, and environmental monitoring, and future prospects.

Keywords:
absolute quantificationdigital PCRsingle molecule

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Area of Science:

  • Molecular Biology
  • Biotechnology
  • Nucleic Acid Detection

Background:

  • Polymerase Chain Reaction (PCR) technologies have evolved, leading to diverse molecular biology applications.
  • Digital PCR (dPCR) amplifies nucleic acids individually using partitioned reactions (wells or droplets).
  • dPCR enables absolute quantification of nucleic acid concentrations without requiring calibrators or standard curves.

Purpose of the Study:

  • To provide a comprehensive overview of Digital PCR (dPCR) technology.
  • To detail the historical development, underlying principles, and various instrument platforms of dPCR.
  • To summarize current and potential future applications of dPCR.

Main Methods:

  • Review of technological advancements in PCR-based nucleic acid detection.
  • Detailed explanation of the dPCR principle and its operational mechanisms.
  • Exploration of different dPCR instrument platforms.

Main Results:

  • dPCR demonstrates high sensitivity, specificity, and accuracy in nucleic acid quantification.
  • Key applications include precise GMO quantification, disease diagnostics, and environmental/food safety monitoring.
  • The technology's potential for future development and utilization is highlighted.

Conclusions:

  • Digital PCR represents a significant advancement in nucleic acid detection and quantification.
  • Its high precision and sensitivity make it valuable across various scientific and industrial fields.
  • Further development of dPCR promises expanded applications and improved analytical capabilities.