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首页> 外文期刊>Biologicals: Journal of the International Association of Biological Standardization >A highly sensitive internally-controlled real-time PCR assay for mycoplasma detection in cell cultures
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A highly sensitive internally-controlled real-time PCR assay for mycoplasma detection in cell cultures

机译:用于支原体在细胞培养物中的高度敏感的内部受控实时PCR测定

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摘要

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.
机译:支原体细胞系的污染是一种常见的发生,并且可以以各种方式影响细胞系行为。 用支原体的污染通常不明显,因此应经常测试细胞系。 存在几种用于支原体检测的商业套件,但pH值。欧元。 培养方法可能需要几周才能产生结果仍被认为是“金标准”方法。 因此,需要快速替代方法,具有可比灵敏度,特异性和物种范围。 在这里,我们描述了用于细胞培养基的基于内部控制的Taqman的实时PCR测定,而不需要DNA提取。 测定可以检测哺乳动物细胞培养物中最常遇到的mycoplasma污染物的少于10 cfu。 经过验证的测定具有在基于细胞培养的生物学生产中作为常规测试的可能性。

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