Literature DB >> 31956000

A highly sensitive internally-controlled real-time PCR assay for mycoplasma detection in cell cultures.

Julia Sung1, J Ross Hawkins2.   

Abstract

Mycoplasma contamination of cell lines is a common occurrence and may affect the cell line behaviour in a variety of ways. Contamination with mycoplasma is usually not obvious so cell lines should be frequently tested. Several commercially available kits for mycoplasma detection exist, however the Ph. Eur. culture method which can take several weeks to yield results is still considered to be the 'gold standard' method. There is therefore a need for rapid alternative methods with comparable sensitivity, specificity and species range. Here, we describe an internally-controlled Taqman-based real-time PCR assay for cell culture medium without the need for DNA extraction. The assay can detect less than 10 CFU of the most frequently encountered mycoplasma contaminants in mammalian cell cultures. The validated assay has the potential to be used as a routine test in the production of cell culture-based Biologicals.
Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

Entities:  

Keywords:  European pharmacopeia; Mycoplasma; qPCR assay

Mesh:

Substances:

Year:  2020        PMID: 31956000     DOI: 10.1016/j.biologicals.2019.12.007

Source DB:  PubMed          Journal:  Biologicals        ISSN: 1045-1056            Impact factor:   1.856


  4 in total

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Authors:  Jiayi Huang; Liang Cui; Meenubharathi Natarajan; Paul W Barone; Jacqueline M Wolfrum; Yie Hou Lee; Scott A Rice; Stacy L Springs
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Review 3.  Scalable Manufacturing of CAR T cells for Cancer Immunotherapy.

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4.  Aptamer Cocktail to Detect Multiple Species of Mycoplasma in Cell Culture.

Authors:  Quanyuan Wan; Xiaohui Liu; Zihua Zeng; Zhenghu Chen; Yanting Liu; Youli Zu
Journal:  Int J Mol Sci       Date:  2020-05-27       Impact factor: 5.923

  4 in total

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