Rapid identification and authentication of closely related animal cell culture by polymerase chain reaction

Animal cell lines are important resources for research and diagnostic applications. Cross-contamination and misidentification of cell lines, however, can cause major problems for research (for example, false results that come from contamination cells may mislead the science). Hence, it is imperative...

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Veröffentlicht in:In vitro cellular & developmental biology. Animal 2008-07, Vol.44 (7), p.224-227
Hauptverfasser: Liu, Merry, Liu, Hsi, Tang, Xiaoling, Vafai, Abbas, Sato, J. Denry
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Sprache:eng
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Zusammenfassung:Animal cell lines are important resources for research and diagnostic applications. Cross-contamination and misidentification of cell lines, however, can cause major problems for research (for example, false results that come from contamination cells may mislead the science). Hence, it is imperative to routinely monitor cell lines for identity and authenticity. Here, we extend our previous work on identification and authentication of animal cell culture by polymerase chain reaction (PCR) amplification and DNA sequencing. A PCR-based method for rapid identification and authentication of closely related cell lines was described. In this method, two new primers were designed based on high homology in the aldolase gene family. Used together with our previous primers, the combinations of primers were able to differentiate closely related species, including human from monkey and mouse from rat. This PCR assay provides a rapid, simple, sensitive, and cost-effective method for authentication of closely related cell lines.
ISSN:1071-2690
1543-706X
DOI:10.1007/s11626-008-9121-1