Baum K F, Berens R L, Jones R H, Marr J J
Department of Medicine, University of Colorado Health Sciences Center, Denver 80262.
J Parasitol. 1988 Apr;74(2):267-9.
This report describes a method of cloning Giardia lamblia by limiting dilution which is simpler than the previously described semisolid agar technique and which may also be applied as an assay of cell viability. A discussion of the basic statistics of limiting dilution, which is applicable to any cell type, and a method of statistically comparing colony-forming efficiencies from different cell populations are included. The colony-forming efficiency (CFE) of this method, when applied to late log-phase cultures, is 72.1 +/- 10.05%. When only cells adherent to the sides of culture vials are cloned, the CFE is 87.1 +/- 9.85%.
本报告描述了一种通过有限稀释法克隆蓝氏贾第鞭毛虫的方法,该方法比先前描述的半固体琼脂技术更简单,并且也可用作细胞活力测定。文中包含了适用于任何细胞类型的有限稀释基本统计学讨论,以及一种对来自不同细胞群体的集落形成效率进行统计学比较的方法。当将该方法应用于对数后期培养物时,其集落形成效率(CFE)为72.1±10.05%。当仅克隆贴壁于培养瓶壁的细胞时,CFE为87.1±9.85%。