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转染ASB 8ΔSB的SPC A1肺癌细胞的增殖速度显著慢于对照组细胞 (P <0 .0 1) ,而转染ASB 8的肺癌细胞没有明显的生长特性改变 ;收藏指正
2.ResultsExpression of Fas mRNA and protein in CTLL 2 cells was reduced to 50% after transfection with anti Fas ribozyme. Being treated with anti Fas antibody (JO 2 ), compared with control and mock transfected cells, viability of CTLL 2 cells transfected with anti Fas ribozyme increased by 1 fold, caspase 3 activity and apoptosis rate of ribozyme transfected cells decreased to 50% and 37%, respectively, and cell killing activity was enhanced by 2 fold.
结果锤头状核酶基因导入CTLL 2细胞后 ,可使其表面的Fas表达降低达 5 0 % ,细胞经Fas抗体 (JO2 )处理后 ,与空白对照、转染空载体的细胞相比 ,转染核酶的细胞增殖活性增加了 1倍 ,caspase 3活性降低近 5 0 % ,而细胞的凋亡率显著降低 ,只有 37% ,且CTLL 2细胞的体外杀伤活性为对照组的 2倍。收藏指正
3.MTT assay showed that the IC50 values for cDDP and ADM were re duced to approximate 86.2%and 99.2%in the transfected cells compared with the untransfected cells, respectively. The low concentration of chemotherapeutic dru gs (1.25 ?ol/L cDDP or 0.05 ?ol/L ADM) without inhibition essentially suppre ssed the growth of the transfected cells markedly.
MTT实验提示顺铂和阿霉素的IC50值分别减少了86.2%和99.2%,转染细胞在原本没有明显抑制和杀伤作用的药物浓度(1.25μmol/L的顺铂或0.05μmol/L的阿霉素)作用下生长明显受到抑制。收藏指正
4.Results:PSVL hFASL transfected cells had the expression of human FAS ligand mRNA, PSVL mock transfected cells was negative There is expression of FAS antigen on the surface of U937 cells With U937 cell line as target, the activity of recombinant human FAS ligand (rhFASL) was assayed After coculture of U937 cells with FASL transfected COS 7, the target cells appeared apoptosis phenomenom Conclusion:Recombinant FasL on the surface of COS 7 cells can be used as functional study
结果:转染后COS?7 细胞有FASL的mRNA 的表达,在COS?7 细胞上表达的重组FASL能诱导FAS阳性的U937 细胞发生程序性死亡。 结论:在COS?7 细胞表面表达的重组FASL分子能用于进一步功能研究和FAS系统拮抗剂的筛选。收藏指正
5.Results There was a significant reduction of tumor size as compared with that in other six control groups ( P<0 001,P<0 05 ). Between animals treated with liptk ACK and tk ACV,there was a significant difference ( P <0 02)). No significant difference was observed in terms of growth rate of tumors among other six control groups ( P <0 05).
结果 瘤体内基因转染后脂质体介导的pLXT、ACV治疗组及裸pLXT注射、ACV治疗组平均瘤体积均显著小于其它六组对照组 (P <0 0 0 1,P <0 0 5 ) ,前两者比较亦有显著差异 (P <0 0 2 )。收藏指正
6.The most remarkable inhibition effect was observed by 5 or 10 μmol/L 4 HPR for 96 h ( P <0.01). Compared with control group,the survival rate in 5 μmol/L 4 HPR group was much lower ( P <0.01). 4 HPR significantly decreased the survival rate of ADPKD cyst lining epithelial cells stimulated by HGF.
结果 :与对照组比较 ,4 - HPR抑制了 ADPKD囊肿衬里上皮细胞增殖 ,且呈量效和时效关系 ,5 μmol/ L 或10 μmol/ L 4 - HPR作用 96 h后抑制效果最强 (P<0 .0 1)。收藏指正
7.Results:When the liver cells were transfected with pEGFP-N3TPT1,the bright green florescence in transfected cells was observed. Transfection efficiency was about 30%.
结果:用此重构体转染后,在荧光显微镜下,可见细胞发出明亮的绿色荧光,转染效率约在30%左右。收藏指正
8.3)Construction of nine eucaryotic expressing plasmids carrying the DF1-9,named pCMV/DF1-9. 4) HL60 cells were transfected with pCMV/DFl-9,and the growth inhibition of the transfe-ctant pCMV/DF4-HL60 was observed.
以上结果说明:(1)DFMO抑制多胺生物合成启动了HL60细胞中与分化及凋亡有关基因的表达; (2)DFMO诱导表达的DF4基因可引起HL60细胞发生凋亡,提示DF4可能调控HL60细胞凋亡的基因;收藏指正
9.The CPE of 293 cell was observed after being transfected and gene integration of G1VP7 in continuously multiplied rvAdG1VP7(G) confirmed by PCR and the green fluorescence was observed in the 293 cells by rvAdG1VP7(G) under fluorescent microscope.
转染重组腺病毒DNA的 2 93细胞出现细胞病变 ,经PCR对传代的rvAdG1VP7(G)分析证实 ,有特异性的G1VP7基因整合 ,荧光显微镜能观察到 2 93细胞内有绿色荧光。收藏指正
10.2. GFP expression in co-transfected AAV-293 cells was observed and the titer of rAAV is 106particles/ml measured by that cells expressing green fluorescence were counted and compared with the total number of cells.
. 2.重组表达质粒转染后的AAV-293细胞可检测到报告基因绿色荧光的表达,根据表达荧光的细胞数得到重组病毒的感染性滴度为106 particles/ml。收藏指正