产品名称:U-937细胞hPTPRA基因敲除株
产品简称:U-937 KO-hPTPRA
产品货号:CGKO-M2708
修饰基因:hPTPRA
基因ID:5786
修饰类型:敲除
转导方法:蛋白法
抗性基因:—
克隆类型:杂合子
细胞鉴定:PCR,测序
种属来源:人
组织来源:胸膜/胸腔积液
疾病特征:淋巴瘤细胞
细胞形态:单核细胞
生长特性:悬浮生长
培养体系:RPMI-1640+10%FBS+1%P/S
配套培养基货号:TCH-G368
传代比例:1:3-1:6,每2-3天换液一次
传代周期:48-72 h
培养条件:气相:95%空气+5%CO2,温度:37℃
冻存条件:60%基础培养基+30%FBS+10%DMSO,液氮储存
质量检测:细菌、真菌、支原体检测均为阴性
参考文献:
Ralph P, et al. Lysozyme synthesis by established human and murine histiocytic lymphoma cell lines. J. Exp. Med. 143: 1528-1533, 1976. PubMed: 1083890
. Gene expression during normal and malignant differentiation. London: Academic Press; 1985.
. International symposium on new trends in human immunology and cancer immunotherapy. Paris: Doin Editeurs; 1980.
Koren HS, et al. In vitro activation of a human macrophage-like cell line. Nature 279: 328-331, 1979. PubMed: 450085
Gidlund M, et al. Natural killer cells kill tumour cells at a given stage of differentiation. Nature 292: 848-850, 1981. PubMed: 7266653
Olsson I, et al. Induction of differentiation of the human histiocytic lymphoma cell line U-937 by 1 alpha,25-dihydroxycholecalciferol. Cancer Res. 43: 5862-5867, 1983. PubMed: 6315218
Morimoto H, et al. Overcoming tumor necrosis factor and drug resistance of human tumor cell lines by combination treatment with anti-Fas antibody and drugs or toxins. Cancer Res. 53: 2591-2596, 1993. PubMed: 7684321
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