软琼脂克隆形成率随着照后传代次数的增加而明显增高；
The colony forming efficincy in soft agar increased with the passaging.
观察不同分离条件对表皮细胞生长情况、贴壁率、克隆形成率的影响。
The output of viable cells, rates of adherence to dish, colony forming efficiency(CFE) of the isolated epidermal ce.
Q水经亚沸处理能显著提高ES细胞保持未分化状态的能力，优质胎牛血清能提高ES的AKP阳性度和克隆形成率。
Purification of Milli-Q water by sub-boiling distilled and employment of qualified FBS could increase the AKP staining positive level and total clone formation rate of mouse ES cells.
人外泌汗腺细胞的克隆形成率为7.3%，与人胎儿角质形成细胞（7.7%）比较差异无统计学意义（P>0·05）。
There was no obvious difference in the cell clone efficiency between human fetal eccrine sweat gland cells (7.3%) and human fetal keratinocytes (7.7 %, P>0.05).
结果显示永生化胚胎肝细胞克隆形成率为31.2%，染色体核型分析表明细胞核型无明显异常，软琼脂集落形成试验表明细胞在软琼脂中不能生长。
It is showed that the cell clone-forming rat was 31. 2%. The immortalized human fetal hepatocytes had a normal karyotype and were not able to grow in soft AGAR culture.
计算各组细胞死亡率、细胞生长抑制率、克隆形成率并观察形态学变化，应用凝胶电泳、激光扫描共聚焦显微镜观察分析小叶黑柴胡作用MGC- 803细胞后的细胞DNA含量的改变。
The changes of morphology, death rate, the inhibition rate of cell growth, cloning efficiency were observed. DNA content of MGC-803 were measured with the laser scanning confocal microtechnic.
采用含碱性成纤维细胞生长因子和表皮生长因子培养基先后作用培养的方法形成神经干细胞克隆率最高(0.630%)。
Clone rate of neural stem cells was the highest (0.630%) using ordinal culture of basic fibroblast growth factor and epidermal growth factor.
采用含碱性成纤维细胞生长因子和表皮生长因子培养基先后作用培养的方法形成神经干细胞克隆率最高(0.630%)。
Clone rate of neural stem cells was the highest (0.630%) using ordinal culture of basic fibroblast growth factor and epidermal growth factor.
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