1) PC-3m cell line
PC-3m细胞系
2) PC-3M cells
PC-3M细胞
1.
Knockdown of survivin expression using siRNA inhibits the growth of PC-3M cells;
Survivin-siRNA对前列腺癌PC-3M细胞增殖的抑制作用
2.
METHODS: E2F decoy DNA,ARE decoy DNA and control decoy DNA were transfected into PC-3M cells with lipofectamine,respectively.
方法:采用脂质体lipofectam ine将E2F decoy DNA、ARE decoy DNA和control decoy DNA分别转染PC-3M细胞,MTT检测其对细胞增生的影响,倒置相差显微镜观察细胞形态变化,流式细胞术检测细胞凋亡率,并进行染色体DNA断裂的测定;通过RT-PCR检测转染的PC-3M细胞中c-Myc mRNA、cyc lin D1 mRNA表达水平的变化,通过W estern b lotting检测细胞中c-Myc蛋白、cyc lin D1蛋白表达水平的变化。
3.
METHODS PC-3M cells were treated with DADAG,ODC activity was tested;cell proliferation was evaluated by sulforhodamine B ( SRB) assay;cell cycle distribution was detected by flow cytometry,the expression of Cdc2,Cyclin B1,p-Cdc2(Tyr15),Cdc25C, and Wee1 were detected by Western blot.
目的研究二乙酰二脱水卫矛醇(DADAG)对鸟氨酸脱羧酶(ODC)活性的影响及其对人前列腺癌PC-3M细胞增殖的作用,并初步探讨其可能的分子机制。
3) PC-3M cell
PC-3M细胞
1.
Methods:PC-3M cells were divided into three experimental groups and a control,treated with polypeptide K237 at the concentration of 50,100,200 and 0 μmol/L,respectively,for 48 hours.
目的:研究多肽K237对体外培养的雄激素非依赖性前列腺癌PC-3M细胞的抑制作用,及其可能的作用机制。
2.
ObjectiveTo investigate the effects of PDCD5 combined with mifepristone on proliferation of prostate cancer PC-3M cells.
方法MTT法分别检测10、20、50和100μmol/L MIF作用于PC-3M细胞24~96 h的吸光度(A)值。
3.
Methods:The inhibiting effect of BQ123 on the proliferation of PC-3M cells was observed by MTT assay,erasion trace test and Traswell chamber che-motaxis assay,and its induction of their apoptosis determined by Annexin V-FITC/PI staining and cytometry.
目的:观察内皮素A受体拮抗剂BQ123对转移性前列腺癌(PCa)PC-3M细胞株增殖与凋亡的影响,初步探讨内皮素A受体拮抗剂对转移性PCa细胞的体外抗肿瘤效应。
4) PC-3M
PC-3M人前列腺癌细胞系
5) prostate cancer cell line PC-3M
前列腺癌细胞株PC-3M
6) PC-3 cell line
PC-3细胞系
1.
Objective To establish a PC-3 cell line stably and highly expressing BRP 44.
目的建立稳定高效表达BRP 44的PC-3细胞系。
补充资料：白细胞细胞系
白细胞细胞系
即经白细胞传代建立的永久性细胞系。这种细胞系仍然保留供者的染色体结构。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条