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At 10^(-9)mol/L of the immunotoxin, 3 logs (99.9%) of target cells were killed, but no cytotoxicity on nontarget cells.

在1×10^(-9)mol/L浓度时对靶细胞的杀伤可达到99.9%,而对非靶细胞则无细胞毒作用。

Methods BGC823 cells were co-cultured with the wild type H.pylori and the isogenous mutant,which were called the wild tue strain group and the mutant stain group,respectively.

结果 野生株和突变株Hp攻击BGC823细胞6h,即可引起细胞的形态学变化,48h时均可观察到细胞形态呈分散及蜂鸟样改变。

The Pin1 PPIase domain has shown to specifically isomerize pSer/Thr-Pro peptide bond in a defined subset of phosphoproteins including transcription factors and cell cycle regulator.

Pin1 於是被认为在磷酸化蛋白质之后修饰机制中,扮演著枢角色去调控细胞生反应及正常细胞的细胞分。

In the other hard, it is reported that caspase - 3 has important effect in cell apotosis by destroyiny the cell anti - apoptosis factors ( eg: bcl - 2 ), cell framework (eg: frame protein actin, fodrin, lamin).

此外文献报道,CasPase一3还通过破坏细胞抗凋亡因素(如bel一2),破坏细胞的结构(如结构蛋白aetin、fodrin、larnin)在细胞凋亡中发挥作用。

Results:The cell nucleus and cell organelle of skin Malpighian cell and dermis fibroblast showed irreversible damage under electronmicroscope.

结果:在8000~20000倍电子显微镜下观察,皮肤角质形成细胞及真皮成纤维细胞的细胞核、细胞器都出现不可逆转损伤。

At the mean time,the culture mixed with the fibroid cells which grew well respectively.Fine single layer was formed and covered the whole amniotic membrane on which the LECs grew membranously,and the fibroid cells outgrew the LECs.

同时,生长的上皮细胞中有成纤维样细胞的混杂生长,但各自保持其良好的细胞形态。3周左右形成良好的单层,细胞生长呈膜片状扩展,整个羊膜之上铺满细胞,有明显的扩展界限。

Microglia BV2 was produced by Cell Research Institute of Chinese Academy of Sciences.

实验中小胶质细胞的替代细胞 BV2由中国科学院细胞研究所生产。

Methods To collect 10 specimen residual ear cartilage of microtia patients about 8-year-old and cultured in vitro, dye with toluidine blue and immunohistochemistry of collagen type II.

结果:残耳软骨细胞在体外培养时随代数增加呈异染陛的糖胺多糖减少,第1、3代Ⅱ型胶原阳性细胞比例约68%~71%,第5代为23%、显著降低;冻存后第3代为65%,与同代数的细胞没有差别,100ng/mi浓度的CDMP-1可以将第4代细胞的阳性比例维持在66%,而且冻存和生长因子不会引起细胞周期的变化。

Methods: M-CSF-dependent bone marrow cells were isolated from 5-6 weeks old mice, and cultured in the presence of MCSF (25μg/L) with different concentrations of TNF-α(0, 1, 10, 100 μg/L) for 5 days, the formation of TRAP multinucleated cells was observed. These cells were also cultured in the presence of both RANKL (30 μg/L) and M-CSF (25 μg/L) with or without 10 μg/L TNF-α for4, 5, 6 and 9 days. The number of TRAP multinucleated cells and resorption pits on dentine slices were counted under light microscope.

选用小鼠巨噬细胞集落刺激因子依赖性非附着性骨髓细胞,在含有25μg/L M-CSF和0,1,10,100μg/L TNF-α的α-MEM培养液中培养5d后,观察抗酒石酸酸性磷酸酶染色阳性多核细胞的形成;细胞在含有25μg/L M-CSF和30μg/L sRANKL的α-MEM培养液中进行培养,比较加入和不加入10μg/L TNF-α培养4、5、6和9d后,所形成的TRAP多核细胞的数目和骨吸收面积。

Methods: M-CSF-dependent bone marrow cells were isolated from 5-6 weeks old mice, and cultured in the presence of M-CSF (25 μg/L) with different concentrations of TNF-α(0, 1, 10, 100 μg/L) for 5 days, the formation of TRAP multinucleated cells was observed.

选用小鼠巨噬细胞集落刺激因子依赖性非附着性骨髓细胞,在含有25μg/LM-CSF和0,1,10,100μg/LTNF-α的α-MEM培养液中培养5d后,观察抗酒石酸酸性磷酸酶染色阳性多核细胞的形成;细胞在含有25μg/LM-CSF和30μg/LsRANKL的α-MEM培养液中进行培养,比较加入和不加入10μg/LTNF-α培养4、5、6和9d后,所形成的TRAP多核细胞的数目和骨吸收面积。

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The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了,排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意,我建议我们在价格上大家各让一半。

After an hour and no pup, look for continued contractions and arching of the back with no pup as a sign of trouble.

一个小时后,并没有任何的PUP ,寻找继续收缩和拱的背面没有任何的PUP作为一个注册的麻烦。