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荧光素酶/GFP标记的人原髓细胞白血病细胞(HL-60-Luc-GFP)
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类型
细胞系
产品货号
TCH-C204LG
品牌
HyCyte®
价格
2800.00
细胞别名
HL 60; HL.60; HL60
库存量
100
规格
1X10^6
用途
仅供科研使用

该细胞由CollinsSJ从一位患有急性早幼粒细胞性白血病的36岁白人女性的外周血中分离建立;可自发分化,或在丁酸盐、次黄嘌呤、佛波醇肉豆蔻酸(PMA,TPA)、DMSO(1%to1.5%)、放线菌素D和视黄酸的刺激下发生分化;PMA刺激后可分泌TNF-α。该细胞具有吞噬活性和趋化反应,癌基因myc阳性,表达补体受体和FcR。所供 Luciferase 稳转细胞株采用VirusFree系统构建,除稳定高效地表达 luciferase 基因外,还具有特异性强、成像质量高、发光强度可精确定量等优点,可实现包括启动子活性研究、哺乳动物细胞双杂交实验以及活体动物成像实验等多方面的灵活应用。

基因报告系统广泛应用于真核生物基因表达和细胞生理学的研究,是提高实验准确度的常用方法。荧光素酶(Luciferase)是以荧光素(luciferin)或脂肪醛(firefly aldehyde)为底物来检测荧光素酶活性的一种常见基因报告系统,因其具有方便快捷、灵敏度强、成功率高等优点,在基因表达的研究中得到广泛应用。


细胞名称:荧光素酶/GFP标记的人原髓细胞白血病细胞

细胞简称HL-60

产品货号TCH-C204LG

转染方法:VirusFree 系统

抗性:Puro

靶细胞名称:HL-60

靶细胞别名:HL 60; HL.60; HL60

种属来源

组织来源外周血

疾病特征急性粒-单核细胞白血病

细胞形态髓母细胞样

生长特性悬浮生长

培养体系IMDM+20%FBS+0.5 ug/mL Puromycin+1%P/S

配套培养基货号:TCH-G204L

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:

"Gallagher R, et al. Characterization of the continuous, differentiating myeloid cell line (HL-60) from a patient with acute promyelocytic leukemia. Blood 54: 713-733, 1979. PubMed: 288488

Collins SJ, et al. Terminal differentiation of human promyelocytic leukemia cells induced by dimethyl sulfoxide and other polar compounds. Proc. Natl. Acad. Sci. USA 75: 2458-2462, 1978. PubMed: 276884

Collins SJ, et al. Continuous growth and differentiation of human myeloid leukaemic cells in suspension culture. Nature 270: 347-349, 1977. PubMed: 271272

Aggarwal BB, et al. Human tumor necrosis factor. Production, purification, and characterization. J. Biol. Chem. 260: 2345-2354, 1985. PubMed: 3871770

Nahm MH, et al. Identification of cross-reactive antibodies with low opsonophogocytic activity for Streptoccus pneumoniae. J. Infect. Dis. 176: 698-703, 1997. PubMed: 9291318

Berninghausen O, Leippe M. Necrosis versus apoptosis as the mechanism of target cell death induced by Entamoeba histolytica. Infect. Immun. 65: 3615-3621, 1997. PubMed: 9284127

Aparicio CL, et al. Correction for label leakage in fluorimetric assays of cell adhesion. BioTechniques 23: 1056-1060, 1997. PubMed: 9421636

Mansat V, et al. The protein kinase C activators phorbol esters and phosphatidylserine inhibit neutral aphingomyelinase activation, ceramide generation, and apoptosis triggered by daunorubicin. Cancer Res. 57: 5300-5304, 1997. PubMed: 9393753

Cuthbert JA, Lipsky PE. Regulation of proliferation and Ras localization in transformed cells by products of mevalonate metabolism. Cancer Res. 57: 3498-3504, 1997. PubMed: 9270019

Michael JM, et al. Resistance to radiation-induced apoptosis in Burkitt's lumphoma cells is associated with defective ceramide signaling. Cancer Res. 57: 3600-3605, 1997. PubMed: 9270034

Clark RA, et al. Tenascin supports lymphocyte rolling. J. Cell Biol. 137: 755-765, 1997. PubMed: 9151679

Tiffany HL, et al. Enhanced expression of the eosinophil-derived neurotoin ribonuclease (RNS2) gene requires interaction between the promoter and intron. J. Biol. Chem. 271: 12387-12393, 1996. PubMed: 8647842

Chan YJ, et al. Synergistic interactions between overlapping binding sites for the serum response factor and ELK-1 proteins mediate both basal enhancement and phorbol ester responsiveness of primate cytomegalovirus. J. Virol. 70: 8590-8605, 1996. PubMed: 8970984

Mao M, et al. RIG-E, a human homolog of the murine Ly-6 family, is induced by retinoic acid during the differentiation of acute promyelocytic leukemia cell. Proc. Natl. Acad. Sci. USA 93: 5910-5914, 1996. PubMed: 8650192

Lepley RA, et al. Tyrosine kinase activity modulates catalysis and translocation of cellular 5-lipoxygenase. J. Biol. Chem. 271: 6179-6184, 1996. PubMed: 8626407

Chen H, et al. Octamer binding factors and their coactivator can activate the murine PU.1 (spi-1) promoter. J. Biol. Chem. 271: 15743-15752, 1996. PubMed: 8663022

U.S. Pharmacopeia USP Monographs: Technetium 99mTc Fanolesomab Injection. Rockville, MD: USP32-NF27, 2005"


收货当天如何处理细胞?

收到细胞后请务必仔细阅读产品资料,了解细胞相关信息,如贴壁特性 (贴壁/悬浮/半贴壁半悬浮)、细胞形态、培养体系、传代比例和换液频率等。

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