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2 protocols using egi 1 acc 385

1

Establishment and Characterization of Biliary Tract Cancer Cell Lines

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A panel of ten BTC cell lines was used in this study: EGI-1 (ACC 385 [32 (link)]) and TFK-1 (ACC 344 [33 (link)]) cells were purchased from the German Collection of Microorganisms and Cell Cultures (DSMZ; https://www.dsmz.de, last accessed on 1 August 2021); HuCCT1 (JCRB0425 [34 (link)]), HuH28 (JCRB0426 [35 (link)]), KKU-055 (JCRB1551), KKU-100 (JCRB1568 [36 (link)]), KKU-213 (JCRB1557 [37 (link)]), NOZ (JCRB1033 [38 ]), OCUG-1 (JCRB0191 [39 (link)]) and OZ (JCRB1032 [40 (link)]) were purchased from the Japanese Collection of Research Bioresources Cell Bank (JCRB; https://cellbank.nibiohn.go.jp, last accessed on 1 August 2021). The immortalized human cholangiocyte cell line MMNK-1 (JCRB1554 [41 (link)]) was purchased from JCRB. All cell lines were cultured in L-glutamine-free Dulbecco’s Modified Eagle Medium (DMEM) containing 4.5 g/L glucose (Gibco, Thermo Fisher Scientific, Waltham, MA, USA). Medium was supplemented with 10% fetal bovine serum (FBS; Serana Europe GmbH, Pessin, Germany) and 1% penicillin/streptomycin (Gibco, Thermo Fisher Scientific, Waltham, MA, USA). Cells were cultured at standard conditions (37 °C, 21% O2, 5% CO2, and 98% humidity).
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2

Establishment and Culture of BTC Cell Lines

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Human BTC cell lines HuCC-T1 (JCRB0425 [29 ]), HuH-28 (JCRB0426 [30 ]), OCUG-1 (JCRB0191 [31 (link)]), OZ (JCRB1032 [32 (link)]), NOZ (JCRB1033 [33 (link)]), KKU-055 (JCRB1551), KKU-100 (JCRB1568 [34 (link)]), KKU-213 (JCRB1557), and immortalized human cholangiocyte cell line MMNK-1 (JCRB1554 [35 (link)]) were purchased from the Japanese Collection of Research Bioresources Cell Bank (JCRB). Human BTC cell lines EGI-1 (ACC385) and TFK-1 (ACC344 [36 (link)]) were purchased from the German Collection of Microorganisms and Cell Cultures GmbH (DSMZ). All cell lines were cultured in L-glutamine-free Dulbecco’s Modified Eagle Medium (DMEM) containing 4.5 g/l glucose (Catalogue #: 11,960,044, Gibco, Thermo Fisher Scientific, Vienna, Austria). Medium was supplemented with 10% foetal bovine serum (FBS; Catalogue #: S-FBS-SA-015, Serana Europe GmbH, Pessin, Germany) and 1% Penicillin-Streptomycin (Catalogue #: P4333, Sigma-Aldrich Handels GmbH, Vienna, Austria). Cells were cultured under standard conditions (37°C, 21% O2, 5% CO2, and 98% humidity).
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