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1)  K562/DOX cell line
K562/DOX细胞株
2)  K562/Dox cell
K562/Dox细胞
1.
OBJECTIVE To develop a method using HPLC with fluorescence detector for determining the Doxorubicin concentrations in K562/DOX cell nuclei.
方法分离K562/DOX细胞核,多柔比星浓度测定采用Diamond C18色谱柱,甲醇-水-醋酸(50∶50∶0。
2.
Methods To detect the survival rate of K562/DOX cell,which was dealt with ADM alone or with both ADM and Chinese Magnolivine Fruit Extraction.
方法MTT法检测单独应用阿霉素或阿霉素与五味子提取物联合作用的K562/DOX细胞的生存率;RT-PCR检测MDR1、MRP1 mRNA表达;Westernblotting检测MDR1蛋白的表达。
3)  K562 cell line
K562细胞株
1.
Cytotoxicity of cord blood monocyte-macrophage activated by cytokines against K562 cell line;
细胞因子激活的脐血单核细胞对K562细胞株杀伤作用的观察
2.
Aim To explore the effect of 4-amino-2-trifluoromethyl-phenyl retinate(ATPR)on proliferation,differentiation activity in K562 cell line,and to research the mechanisms.
目的本研究探讨新型维甲酸衍生物4-氨基-2-三氟甲基苯基维甲酸酯(4-amino-2-trifluoromethyl-phenyl retinate,ATPR)对K562细胞株的抑制增殖和诱导分化活性并对其机制进行研究。
4)  cell line K562
细胞株K562
5)  K562
K562细胞株
1.
Effect of Antisense-oligodeoxynucleotide Aimed hTERT on Telomerase Activity and Cell Apoptosis in K562 Cell Line;
反义寡核苷酸靶向hTERT对K562细胞株端粒酶活性和细胞凋亡的影响
6)  K562/A02 cell line
K562/A02细胞株
1.
Research of expression of p16 gene in K562/A02 cell line;
p16基因在K562/A02细胞株表达情况的研究
补充资料:细胞株
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性质:用单细胞分离培养法或克隆形成法从原代培养或从细胞系所选出的细胞群,称细胞株。一个细胞株应具有特定的生物学性质和标记并持续存在。

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