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The MM134 is a laboratory equipment product designed for cell culture applications. It provides a controlled environment for culturing cells, with functions to regulate temperature, humidity, and gas levels. The core purpose of the MM134 is to facilitate the growth and maintenance of cells in a laboratory setting.

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2 protocols using mm134

1

Maintenance and Hormone Deprivation of Breast Cancer Cell Lines

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MCF-7 and T47D (ATCC) were maintained as described (16 (link)). MM134 (ATCC) were maintained in 1:1 DMEM:L-15 (Life Technologies) +10% FBS. SUM44PE (Asterand) were maintained as described (17 (link)) +2% charcoal stripped serum (CSS). Cell lines are authenticated annually by PCR RFLP analyses at the University of Pittsburgh Cell Culture and Cytogenetics Facility, and confirmed to be mycoplasma-negative. Authenticated cells are in continuous culture for <6mo. Cells were hormone-deprived as described (16 (link)) in phenol red-free IMEM with 5%, 10%, or 2% CSS for MCF-7, MM134, and SUM44, respectively.
17β-estradiol (E2), tamoxifen free-base, 4-hydroxytamoxifen (4OHT), and endoxifen (Bx) were obtained from Sigma. Lapatinib and lasofoxifene were obtained from Santa Cruz Biotechnology. All other compounds were obtained from Tocris Biosciences. E2, tamoxifen, 4OHT, Bx, and ICI were dissolved in ethanol; all other compounds were dissolved in DMSO.
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2

Breast Cancer Cell Line Culture

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The ER+ lobular breast cancer cell line MDA-MB-134 (MM134) was purchased from the ATCC. MM134 cells were cultured in DMEM:Leibovitz-15 1:1 media supplemented with 10% FBS and 1% penicillin/streptomycin. MCF7 breast cancer cell line (HER2 WT or the L755S HER2-activating mutation) were previously isogenically modified using AAV-mediated gene targeting as previously described (16 (link)). These MCF7 breast cancer cells were gifts from Dr. Ben Ho Park (Vanderbilt University Medical Center, Nashville, TN). These cells were cultured in IMEM supplemented with 10% FBS and 1% penicillin/streptomycin. SUM44PE cells were purchased from BIOIVT. SUM44PE parental or CRISPR knock in (KI) V777L and L755S cells were cultured in Ham's F12 media with 2% FBS and 1% penicillin/streptomycin supplemented with all the additional components listed in Supplementary Table S2 as per BIOIVT recommendations. For low E2 growth conditions, the appropriate phenol-red-free medium supplemented with 5% charcoal-dextran-stripped serum was used. All cell lines were cultured in 5% CO2 at 37°C and were examined every 6 months for Mycoplasma.
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