Tucker Ben, Lardelli Michael
ARC Special Research Center for the Molecular Genetics of Development and Discipline of Genetics, School of Molecular and Biomedical Science, The University of Adelaide, Adelaide, Australia.
Zebrafish. 2007 Summer;4(2):113-6. doi: 10.1089/zeb.2007.0508.
The ability to easily analyze apoptosis is important in studies of molecular cell biology and to evaluate the relative toxicity of different treatments or environments. This is particularly the case when substances such as morpholino oligonucleotides are injected into embryos, as such treatments can cause widespread, complex patterns of apoptosis. Zebrafish embryos are well suited for cell biological and environmental toxicity analyses, but the need remains for a simple method that can analyze levels of apoptosis in a statistically significant number of embryos. Here we present a "group fluorescence" method for rapid, large-scale analysis of relative levels of apoptosis based on densitometric techniques.
在分子细胞生物学研究以及评估不同处理或环境的相对毒性时,能够轻松分析细胞凋亡非常重要。当诸如吗啉代寡核苷酸等物质被注射到胚胎中时,情况尤其如此,因为此类处理可导致广泛、复杂的细胞凋亡模式。斑马鱼胚胎非常适合进行细胞生物学和环境毒性分析,但仍需要一种简单的方法,能够在具有统计学意义数量的胚胎中分析细胞凋亡水平。在此,我们基于密度测定技术,提出一种用于快速、大规模分析细胞凋亡相对水平的“群体荧光”方法。