Laboratory Exercise to Measure Plasmid Copy Number by qPCR

Author:

David Benjamin1ORCID,Li Jinbei1ORCID,Masood Faisal12ORCID,Blassick Caroline13ORCID,Jensen Paul14ORCID,Jensen Karin1ORCID

Affiliation:

1. Department of Bioengineering, University of Illinois Urbana-Champaign, Urbana, Illinois, USA

2. College of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA

3. Department of Biomedical Engineering, Boston University, Boston, Massachusetts, USA

4. Carl R. Woese Institute for Genomic Biology, University of Illinois Urbana-Champaign, Urbana, Illinois, USA

Abstract

Quantitative PCR (qPCR) has numerous applications in biology. In an education setting, qPCR provides students an opportunity to better understand the PCR mechanism by providing both quantitative information about the reactions and also data to troubleshoot PCRs (e.g., melt curves). Here, we present a relatively short (2-h) laboratory activity to demonstrate qPCR to quantify plasmid copy number (CN) by measuring the cycle threshold ( C T ) values for a genomic gene and a plasmid gene using transformed cells as a template. The activity can be combined with additional laboratory exercises, including bacterial transformation, to create the template to be used in the qPCRs. This lab activity is ideal for undergraduate laboratory courses that include recombinant DNA technology.

Publisher

American Society for Microbiology

Subject

General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Education

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