There was no cell clone observed in soft agar.
软琼脂培养无克隆形成。
Soft agar assay and nude mouse tumorigenicity assay were carried out.
软琼脂集落形成试验和裸鼠成瘤试验。
Methods Soft AGAR assay and nude mouse tumorigenicity assay were used.
方法软琼脂集落形成试验和裸鼠成瘤实验。
The colony forming efficincy in soft agar increased with the passaging.
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 morpho- logically transformed cells could grow in colony on soft agar.
得到的转化细胞能在软琼脂板上生长；
The cell growth and soft AGAR assay were run to test the transformed cells.
通过细胞形态、软琼脂集落形成实验检测细胞的转化。
Methods Anchorage-independent adhesion among cells was examined in soft agar culture.
方法软琼脂培养观察非锚定状态下细胞间的粘附；
The infected cells (293-bk cells) grew as well as other 293 cells, and formed colony in soft AGAR 14 days later.
感染细胞(称作293-BK细胞)如其他293细胞一样生长，14天后可在软琼脂中形成细胞集落。
The transformed cells separated from the foci lost their ability of post-confluence inhibition of division, and could grow into colony in soft AGAR medium.
从转化灶中分离的细胞，失去了在培养中的接触抑制，能在软琼脂培养基中形成集落。
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.
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。
The carcinogenicity of nickel compounds on human epithelial cells was identified by transforming assay, assay for culture on soft AGAR and test of tumorigenicity in nude mice.
研究几种镍化合物对培养人支气管上皮细胞的恶性转化作用及转化细胞的致癌性。
Results During long term cultivation, the population doubling time of the cells became shorter and the percentage of aneuploidy chromosomes and colonies grown in soft AGAR increased.
结果卵圆细胞在培养过程中倍增时间逐渐缩短，非整倍体染色体数目增加，在软琼脂中生长的克隆增多。
The transformed cells were able to form colonies in soft-agar medium.
转化细胞在软琼脂培养基有细胞集落形成。
The transformed cells were able to form colonies in soft-agar medium.
转化细胞在软琼脂培养基有细胞集落形成。
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