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通过流动微荧光法对棘阿米巴中总细胞DNA进行定量分析。

Quantation by flow microfluorometry of total cellular DNA in Acanthamoeba.

作者信息

Coulson P B, Tyndall R

出版信息

J Histochem Cytochem. 1978 Sep;26(9):713-8. doi: 10.1177/26.9.361883.

Abstract

The DNA content of five species of Acanthamoeba was determined by flow microfluorometry. Acanthamoeba castellanii (AC-30), acanthamoeba polyphaga (APG and P-23), acanthamoeba rhysodes, acanthamoeba culbertsoni (A-1), and acanthamoeba royreba were grown in a casitone based medium 24-48 HR. The trophozoites were harvested, and evaluated for DNA-bound fluorescence. All species tested has DNA values between 2.0-5.0 pg/cell. These results placed DNA/cell values of Acanthamoeba slightly lower than DNA/cell values of other eucaryotic cells and much lower than Amoeba proteus values. These results indicate that FMF may be a useful adjunct in distinguishing Acanthamoeba cells from either eucaryotic cells or some other amoeba. However, differences in DNA/cell between species of Acanthamoeba are small and would not be useful in identification of species.

摘要

通过流式细胞荧光测定法测定了五种棘阿米巴属的DNA含量。卡氏棘阿米巴(AC - 30)、多噬棘阿米巴(APG和P - 23)、里斯棘阿米巴、库氏棘阿米巴(A - 1)和罗伊雷巴棘阿米巴在基于酪蛋白氨基酸的培养基中培养24 - 48小时。收集滋养体,并评估其与DNA结合的荧光。所有测试的物种的DNA值在2.0 - 5.0 pg/细胞之间。这些结果表明棘阿米巴属的DNA/细胞值略低于其他真核细胞的DNA/细胞值,且远低于变形虫的值。这些结果表明,流式细胞荧光测定法可能是区分棘阿米巴属细胞与真核细胞或其他一些变形虫的有用辅助方法。然而,棘阿米巴属不同物种之间的DNA/细胞差异很小,在物种鉴定中没有用处。

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