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细胞培养中支原体污染检测的问题(作者译)

[Problems in detection of mycoplasma contamination in cell cultures (author's transl)].

作者信息

Bonissol C, Gilbert M, Ivanova L M

出版信息

Ann Microbiol (Paris). 1978 Aug-Sep;129B(2):245-65.

PMID:82418
Abstract

A total of 135 cell lines was examined for mycoplasma contamination using two techniques: isolation and specific DNA-staining with DAPI or "Hoechst 33258". The two techniques showed similar results in 64% of the cases of cell contamination while the remainder was detected only by one or the other techniques: 12,82% by the staining technique and 23% by the isolation technique, which shows that the 2 techniques are complementary. The staining technique is very quick, easy to execute, very sensitive, and should be the method of choice to detect contamination when the mycoplasma do not grow in acellular media.

摘要

使用两种技术对总共135个细胞系进行支原体污染检测:分离培养法以及用4',6-二脒基-2-苯基吲哚(DAPI)或“Hoescht 33258”进行特异性DNA染色法。在64%的细胞污染案例中,这两种技术显示出相似的结果,而其余案例仅通过其中一种技术检测到:12.82%通过染色技术检测到,23%通过分离培养技术检测到,这表明这两种技术具有互补性。染色技术非常快速、易于操作、灵敏度高,当支原体在无细胞培养基中不生长时,它应该是检测污染的首选方法。

相似文献

1
[Problems in detection of mycoplasma contamination in cell cultures (author's transl)].细胞培养中支原体污染检测的问题(作者译)
Ann Microbiol (Paris). 1978 Aug-Sep;129B(2):245-65.
2
Comparison of methods used for detection of mycoplasma contamination in cell cultures, sera, and live-virus vaccines.用于检测细胞培养物、血清和活病毒疫苗中支原体污染的方法比较。
Folia Biol (Praha). 1993;39(5):270-6.
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Use of Hoechst 33258 fluorochrome for detection of mycoplasma contamination in cell cultures: development of a technique based on simultaneous fixation and staining.使用Hoechst 33258荧光染料检测细胞培养物中的支原体污染:基于同步固定和染色的技术开发
Boll Ist Sieroter Milan. 1980 May 31;59(2):155-8.
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[Mycoplasma contamination of cell cultures: methods for its detection and the possible routes of Mycoplasma infection spread].[细胞培养中的支原体污染:检测方法及支原体感染传播的可能途径]
Tsitologiia. 1985 Mar;27(3):276-81.
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Rapid detection of mycoplasma in continuous cell lines using a selective biochemical test.使用选择性生化试验快速检测连续细胞系中的支原体
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Experience with testing for mycoplasma with five different methods.使用五种不同方法检测支原体的经验。
Dev Biol Stand. 1979;42:55-9.
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Mycoplasma detection in cell cultures: a comparison of four methods.细胞培养物中的支原体检测:四种方法的比较
Br J Biomed Sci. 2000;57(4):295-301.
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Detection of mollicute contamination in cell cultures by 16S rDNA amplification.通过16S rDNA扩增检测细胞培养物中的支原体污染
Mol Cell Probes. 1993 Jun;7(3):209-16. doi: 10.1006/mcpr.1993.1030.
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[Porcine Mycoplasma and cell cultures. 3. Staining methods for the demonstration of Mycoplasma in cell cultures and methods for the demonstration of cytopathogenic changes].[猪支原体与细胞培养。3. 细胞培养中支原体检测的染色方法及细胞病变变化的检测方法]
Arch Exp Veterinarmed. 1969;23(3):625-32.
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Cross comparison of rapid mycoplasma detection platforms.快速支原体检测平台的交叉比较
Biologicals. 2010 Mar;38(2):218-23. doi: 10.1016/j.biologicals.2009.11.002. Epub 2010 Feb 11.

引用本文的文献

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Arginine consumption as a monitor of mycoplasma infection of cultured cells.精氨酸消耗作为培养细胞支原体感染的监测指标。
In Vitro Cell Dev Biol Anim. 1995 Jul-Aug;31(7):497-8. doi: 10.1007/BF02634026.
2
Rat pleural mesothelial cells in culture.培养中的大鼠胸膜间皮细胞。
In Vitro. 1981 Feb;17(2):98-106. doi: 10.1007/BF02618065.
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Laminin provides a better substrate than fibronectin for attachment, growth, and differentiation of 1003 embryonal carcinoma cells.层粘连蛋白比纤连蛋白能为1003个胚胎癌细胞的附着、生长和分化提供更好的底物。
In Vitro. 1982 Dec;18(12):997-1003. doi: 10.1007/BF02796374.
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Comparison of two methods for detection of mollicutes (Mycoplasmatales and Acholeplasmatales) in cell cultures in the Netherlands.荷兰细胞培养物中支原体(支原体目和无胆甾原体目)两种检测方法的比较
Antonie Van Leeuwenhoek. 1987;53(2):107-18. doi: 10.1007/BF00419507.