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3 protocols using dmem f12 cell culture media

1

Maintenance of HEK293T and SCLC Cell Lines

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HEK293T cells were obtained from ATCC and then maintained with DMEM (Gibco, Gaithersburg, MD) containing 10% FBS (Sigma). The SCLC cell lines were obtained from ATCC. NCI-H748, NCI-H1963, NCI-H209, NCI-H889, and NCI-H69 cells were maintained with ATCC-formulated RPMI-1640 medium containing 10% FBS (Sigma). NCI-H1882, NCI-H1436, NCI-H1105, and NCI-H2171 cells were maintained with ATCC-formulated DMEM/F12 cell culture media containing 10% FBS (Sigma).
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2

Cell Line Maintenance and Validation

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HEK293T cells were obtained from ATCC, and then maintained with DMEM (Gibco) containing 10% FBS (Sigma). The SCLC cell lines were obtained from ATCC. NCI-H748, NCI-H1963, NCI-H69, NCI-H889, NCI-H196, NCI-H226, and NCI-H209 cells were maintained with ATCC-formulated RPMI1640 medium containing 10% FBS (Sigma). NCI-H1882, NCI-H1105, and NCI-H2171 cells were maintained with ATCC-formulated DMEM/F12 cell culture media containing 10% FBS (Sigma). All cell lines were authenticated through STR profiling and tested bi-weekly for Mycoplasma by PCR. Cell lines were not passaged more than 20 times.
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3

Cell Culture Conditions for Breast Cancer Cell Lines

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The human breast cancer cells MDA-MB 468, BT20, MDA-MB 231, MCF7, T47D, SK-BR-3, HEK-293 and mouse 4T1 breast cancer cells were obtained from the American Type Culture Collection. MDA-MB 468 and HEK-293 cells were maintained in DMEM (Sigma) supplemented with 2 μM L-glutamine (Sigma); BT20 cells were maintained in EMEM (Sigma) supplemented with 1 mM Sodium Pyurvate (Sigma); MDA-MB 231, MCF7, T47D, 4T1 and PBMCs were maintained in RPMI 1640 cell culture media (Sigma); SK-BR-3 cells were maintained in DMEM/F12 cell culture media (Sigma). All culture media were supplemented with 10% FBS and 1% Penicillin-Streptomycin (P+S) and cultures were grown at 37 °C with 5% CO2.
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