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技術(shù)文章

恒遠(yuǎn)產(chǎn)品文獻(xiàn):試劑霍亂毒素引用文獻(xiàn)

點(diǎn)擊次數(shù):14314   發(fā)布時間:2020/12/29 10:24:49

【文獻(xiàn)標(biāo)題】Sphk1 participates in malignant progression of breast cancer by regulating epithelial-mesenchymal transition and stem cell characteristics

【作者】Zhijie Chen, Bingxiong Liu

【作者單位】漢川市人民醫(yī)院(Hanchuan People’s Hospital)

【文獻(xiàn)中引用產(chǎn)品】

霍亂毒素 CAS號:9012-63-9

【關(guān)鍵詞】Breast cancer,Sphingosine kinase 1,Epithelial-mesenchymal transition,Stem cell,Metastasis

【DOI】https://doi.org/10.1016/j.tice.2020.101380

【影響因子(IF)】2.90

出版期刊】《Tissue and Cell》

【產(chǎn)品原文引用】

Cell and culture

Human breast epithelial cells (MCF-10A, CRL-10317) and BC cell lines MCF-7 (CRL-3435), T47D (HTB-133), SKBR3 (HTB-30), MDA-MB-231 (HTB-26), BT-474 (HTB-20) were purchased from American Tissue Culture Collection. The cells, except MDA-MB-23 cells, were cultured in DMEM (12491015, ThermoFisher, USA) containing 10 % FBS (30067334, ThermoFisher, USA), 1% penicillin/streptomycin (15140163,ThermoFisher, USA) at 37 °C in 5% CO2. MCF-10A cell line was cultured with additional 100 ng/mL cholera toxin (Hengyuan,China, http://www.hyswbio.com) on the basis of other cell culture condition. After culture for one day, the original medium was discarded, and the cells were washed 1–2 times by PBS. Next, 5 mL fresh DMEM medium was added and further incubated with the cells in a CO2 incubator. When the confluence reached 80%–90%, the cells were subcultured. MDA-MB-231 cells were cultured in Leibovitz’s L15 medium (11415064, ThermoFisher, USA) without CO2。


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原創(chuàng)作者:上海恒遠(yuǎn)生物技術(shù)發(fā)展有限公司

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