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The DMS153 is a laboratory instrument designed for biomolecular analysis. It utilizes differential mobility spectrometry (DMS) technology to separate and detect ions based on their gas-phase mobility. The core function of the DMS153 is to provide high-resolution ion separation and detection for various analytical applications.

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Lab products found in correlation

Bronchial epithelial growth kit, by American Type Culture Collection (2 mentions) Dms114, by Thermo Fisher Scientific (2 mentions) Waymouth s medium, by Thermo Fisher Scientific (2 mentions) Dulbecco modified eagle medium (dmem), by Thermo Fisher Scientific (2 mentions) Rpmi 1640, by Thermo Fisher Scientific (2 mentions)

2 protocols using dms153

1

Cell Culture Protocols for SCLC Research

Cited 1 time
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All cell lines were originally purchased from the American Type Culture Collection (ATCC, Manassas, VA). Human SCLC cell lines (H128, H146, H187, H69, DMS114 and DMS153) were provided by the laboratory of Dr. Taofeek Owonikoko [47 (link)]. H128, H187, H69, and H146 cells were grown in RPMI 1640 (Gibco) with 7.5% fetal bovine serum (FBS). DMS114 and DMS153 cells were grown in Waymouth’s medium (Gibco) with 5% FBS. HeLa, U2OS, HEK293T, and HCT116 cells were grown in DMEM (Gibco) with 7.5% FBS. BEAS-2B were cultured in DMEM/F-12 medium with 10% FBS. Primary small airway epithelial cells (HSAEC) were grown in Airway Basal Medium (ATCC PCS-300-030) with one Bronchial Epithelial Growth Kit (ATCC PCS-300-040) according to manufacturer’s instructions. All cell lines were grown at 37°C under humidified conditions with 5% CO2 and 95% air.
Details of additional methodologies can be found in Supplementary Materials and Methods.
Koyen A.E., Madden M.Z., Park D., Minten E.V., Kapoor-Vazirani P., Werner E., Pfister N.T., Haji-Seyed-Javadi R., Zhang H., Xu J., Deng N., Duong D.M., Pecan T.J., Frazier Z., Nagel Z.D., Lazaro J.B., Mouw K.W., Seyfried N.T., Moreno C.S., Owonikoko T.K., Deng X, & Yu D.S. (2020). EZH2 has a Non-Catalytic and PRC2-Independent Role in Stabilizing DDB2 to Promote Nucleotide Excision Repair. Oncogene, 39(25), 4798-4813.
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2

Cell Culture Protocols for SCLC Research

Cited 1 time
Check if the same lab product or an alternative is used in the 5 most similar protocols
All cell lines were originally purchased from the American Type Culture Collection (ATCC, Manassas, VA). Human SCLC cell lines (H128, H146, H187, H69, DMS114 and DMS153) were provided by the laboratory of Dr. Taofeek Owonikoko [47 (link)]. H128, H187, H69, and H146 cells were grown in RPMI 1640 (Gibco) with 7.5% fetal bovine serum (FBS). DMS114 and DMS153 cells were grown in Waymouth’s medium (Gibco) with 5% FBS. HeLa, U2OS, HEK293T, and HCT116 cells were grown in DMEM (Gibco) with 7.5% FBS. BEAS-2B were cultured in DMEM/F-12 medium with 10% FBS. Primary small airway epithelial cells (HSAEC) were grown in Airway Basal Medium (ATCC PCS-300-030) with one Bronchial Epithelial Growth Kit (ATCC PCS-300-040) according to manufacturer’s instructions. All cell lines were grown at 37°C under humidified conditions with 5% CO2 and 95% air.
Details of additional methodologies can be found in Supplementary Materials and Methods.
Koyen A.E., Madden M.Z., Park D., Minten E.V., Kapoor-Vazirani P., Werner E., Pfister N.T., Haji-Seyed-Javadi R., Zhang H., Xu J., Deng N., Duong D.M., Pecan T.J., Frazier Z., Nagel Z.D., Lazaro J.B., Mouw K.W., Seyfried N.T., Moreno C.S., Owonikoko T.K., Deng X, & Yu D.S. (2020). EZH2 has a Non-Catalytic and PRC2-Independent Role in Stabilizing DDB2 to Promote Nucleotide Excision Repair. Oncogene, 39(25), 4798-4813.
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