<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>B. C. Lidgerding</dc:contributor>
  <dc:contributor>P. E. McAllister</dc:contributor>
  <dc:contributor>F. M. Hetrick</dc:contributor>
  <dc:creator>C. L. Schultz</dc:creator>
  <dc:date>1986</dc:date>
  <dc:description>&lt;p&gt;&lt;span&gt;Differential incorporation of uridine and uracil was used to assay for mycoplasma contamination in five fish cell lines: bluegill fry (BF-2), chinook salmon embryo (CHSE-214), epithelioma papillosum cyprini (EPC), fathead minnow (FHM) and rainbow trout gonad (RTG-2). The method was not suitable for monitoring BF-2, CHSE-214, FHM, and RTG-2 cell lines because they incorporated uracil. Differential incorporation of uridine and uracil may be applicable for screening EPC cells because only this cell line could distinguish cultures experimentally infected with&amp;nbsp;&lt;/span&gt;&lt;i&gt;Mycoplasma orale&lt;/i&gt;&lt;span&gt;&amp;nbsp;from cultures known to be free from microbial contaminants.&lt;/span&gt;&lt;/p&gt;</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1111/j.1365-2761.1986.tb00990.x</dc:identifier>
  <dc:language>en</dc:language>
  <dc:publisher>Wiley</dc:publisher>
  <dc:title>Mycoplasma contamination in fish cell lines: An evaluation of detection by differential incorporation of 3H-uridine and 14C-uracil</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>