Chazotte Brad
Cold Spring Harb Protoc. 2011 Jan 1;2011(1):pdb.prot5556. doi: 10.1101/pdb.prot5556.
A number of fluorescent stains are available that label DNA and allow easy visualization of the nucleus in interphase cells and chromosomes in mitotic cells, including Hoechst, 4',6-diamidino-2-phenylindole (DAPI), ethidium bromide, propidium iodide, and acridine orange. Although not as bright as the vital Hoechst stains for DNA, DAPI has greater photostability. It is believed that DAPI associates with the minor groove of double-stranded DNA, with a preference for the adenine-thymine clusters. Cells must be permeabilized and/or fixed for DAPI to enter the cell and to bind DNA. Fluorescence increases approximately 20-fold when DAPI is bound to double-stranded DNA. This protocol describes the use of DAPI to label nuclear DNA of cells grown in culture.
有多种荧光染料可用于标记DNA,能轻松观察间期细胞中的细胞核以及有丝分裂细胞中的染色体,包括Hoechst、4',6-二脒基-2-苯基吲哚(DAPI)、溴化乙锭、碘化丙啶和吖啶橙。尽管DAPI对DNA的染色不如活性Hoechst染料明亮,但它具有更高的光稳定性。据信DAPI与双链DNA的小沟结合,尤其偏好腺嘌呤-胸腺嘧啶簇。细胞必须进行通透处理和/或固定,以便DAPI进入细胞并与DNA结合。当DAPI与双链DNA结合时,荧光强度大约会增加20倍。本方案描述了使用DAPI标记培养细胞中核DNA的方法。