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Related Concept Videos

Proofreading01:31

Proofreading

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Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
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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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Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
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Updated: Jul 16, 2025

Genome-wide Purification of Extrachromosomal Circular DNA from Eukaryotic Cells
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Corrigendum: Improved single-cell genome amplification by a high-efficiency phi29 DNA polymerase.

Jia Zhang1,2,3,4, Xiaolu Su1,2,3,4, Yefei Wang2,3,4,5

  • 1Single-Cell Center, CAS Key Laboratory of Biofuels, Shandong Key Laboratory of Energy Genetics, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao, Shandong, China.

Frontiers in Bioengineering and Biotechnology
|September 13, 2023
PubMed
Summary

This study corrects a previous article DOI. The corrected DOI is 10.3389/fbioe.2023.1233856.

Keywords:
GB1 fusion proteindisulfide bondphi29 DNA polymeraseprocess engineering high-efficiency phi29 DNA polymerasesingle-cell genome amplification

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Area of Science:

  • Biomedical Engineering
  • Scientific Publishing

Context:

  • Correction of a previously published article DOI.
  • Ensuring accurate citation and discoverability of scientific literature.

Purpose:

  • To provide the correct Digital Object Identifier (DOI) for a specific publication.
  • To rectify an error in the article's metadata.

Summary:

  • The article DOI has been updated to 10.3389/fbioe.2023.1233856.
  • This correction ensures proper referencing and access to the research.

Impact:

  • Improved accuracy in scientific record-keeping.
  • Facilitates correct citation and retrieval of the research article.