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Emem cell culture media

Manufactured by Corning
Sourced in United States

EMEM (Eagle's Minimum Essential Medium) is a cell culture media formulated for the maintenance and growth of a variety of cell types. It provides the necessary nutrients and growth factors to support cell proliferation and survival in vitro.

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2 protocols using emem cell culture media

1

Prostate Cancer Cell Lines and Fibroblasts: Culture and Maintenance

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Androgen-independent prostate cancer cell lines DU145 (ATCC #HTB-81) and PC3 (ATCC #CRL-1435), androgen-dependent prostate cancer cell line LNCaP (ATCC #CRL-1740), prostate-derived fibroblasts WPMY-1 (ATCC #CRL-2854) and hTERT PF179T (ATCC #CRL-3290) were purchased from American Type Culture Collection (Manassas, VA, USA). DU145 cells were maintained in Eagle’s Minimum Essential Medium (EMEM) cell culture media (Corning, Corning, NY, USA). PC3 cells were cultured in F12 cell culture media (Gibco, ThermoFisher, Waltham, MA, USA). LNCaP cells were cultured in RPMI-1640 culture media (ATCC 30–2001). WPMY-1 normal fibroblast cells were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM). Media was supplemented with 10% (v/v) fetal bovine serum (FBS) and 1% (v/v) Pen Strep (both purchased from Gibco) under humidified conditions at 37°C and 5% CO2. hTERT PF179T cancer-associated fibroblast cells were maintained in EMEM supplemented with 10% (v/v) FBS, 1% (v/v) sodium bicarbonate 7.5% solution (#SH30033.01, GE Life Sciences Hyclone), and 0.01% 10 mg/mL puromycin (#A11138-03, Gibco).
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2

Cell Culture of Prostate Cancer Lines

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Prostate cancer cell lines DU145 (ATCC #HTB-81) and PC3 (ATCC #CRL-1435) were obtained from American Type Culture Collection (Manassas, VA, USA). DU145 cells were maintained in Eagle’s Minimum Essential Medium (EMEM) cell culture media (Corning, Corning, NY, USA). PC3 cells were cultured in F12 cell culture media (Gibco, ThermoFisher, Waltham, MA, USA). Media was supplemented with 10% (v/v) fetal bovine serum (FBS) and 1% (v/v) PenStrep (both purchased from Gibco) under humidified conditions at 37˚C and 5% CO2. All cell lines were obtained in Spring 2018 and placed in liquid nitrogen until required for use. Cells were tested twice using a Mycoplasma Detection Kit (ATCC 30–1012K) following manufacturer’s protocol. Testing occurred once after thawing at passage 3 and then near the end of experiments at passage 15. Test results were negative. Cells were last tested 04/01/2020.
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