流式细胞术
寡核苷酸
16S核糖体RNA
低聚物限制
生物
荧光
核糖体RNA
荧光标记
细菌
分子生物学
荧光原位杂交
荧光显微镜
分子探针
细胞仪
微生物学
DNA
核糖体DNA
遗传学
基因
染色体
物理
量子力学
作者
Rudolf Amann,Brian J. Binder,Robert J. Olson,Sallie W. Chisholm,Richard Devereux,David A. Stahl
标识
DOI:10.1128/aem.56.6.1919-1925.1990
摘要
Fluorescent oligonucleotide hybridization probes were used to label bacterial cells for analysis by flow cytometry. The probes, complementary to short sequence elements within the 16S rRNA common to phylogenetically coherent assemblages of microorganisms, were labeled with tetramethylrhodamine and hybridized to suspensions of fixed cells. Flow cytometry was used to resolve individual target and nontarget bacteria (1 to 5 microns) via probe-conferred fluorescence. Target cells were quantified in an excess of nontarget cells. The intensity of fluorescence was increased additively by the combined use of two or three fluorescent probes complementary to different regions of the same 16S rRNA.
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