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Ben men 1

Manufactured by Leibniz Institute DSMZ
Sourced in Germany

The Ben-Men-1 is a laboratory equipment used for the cultivation and maintenance of anaerobic microorganisms. It provides a controlled environment with low oxygen levels to support the growth of anaerobic bacteria and other obligate anaerobes.

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4 protocols using ben men 1

1

Establishing NCH93 Anaplastic Meningioma Cell Line

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NCH93 tumor cells originated from a 64-year-old man suffering from a relapsed anaplastic meningioma (WHO°III) located in the left parieto-occipital region. The tumor sample was first mechanically dissected. Then the resulting cell suspension was cultured in Dulbecco’s minimal Eagle’s medium supplemented with 10% fetal calf serum (Sigma-Aldrich, St. Louis, MO, USA), 2% L-GlutaMAX (Sigma-Aldrich) and 1% Penicillin/Streptomycin (Sigma-Aldrich). Cells were subcultured in a ratio of 1:10 twice a week. Mycoplasma contamination was excluded by 4′,6-diamidino-2-phenylindole staining (Roche). The benign cell line Ben-Men-1 was purchased from DSMZ (Braunschweig, Germany). Cells were grown in the same medium as NCH93, and both were cultured at 37 °C in a humidified environment in a 5% CO2 atmosphere. Cell lines were authenticated by STR DNA profiling analysis (Leibniz Institute DMSZ, Braunschweig, Germany).
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2

Immortalized Human Meningothelial Meningioma Cell Line

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Human benign meningioma cell line Ben-Men-1 and HEK293T were purchased from DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen, Braunschweig, Germany). Ben-Men-1 was originally established from a meningothelial meningioma after surgical tumor resection [55 (link)]. The cells were immortalized by retroviral transduction with human telomerase reverse transcriptase (hTERT) gene [55 (link)].
Ben-Men-1 and HEK293T cells were cultured in Dulbecco's Modified Eagle Medium (Life Technologies, Carlsbad, CA, USA) supplemented with 10 % (v/v) heat-inactivated fetal bovine serum (FBS; Biochrom, Berlin, Germany) and 1 % (w/v) penicillin/streptomycin (P/S; Life Technologies, Carlsbad, CA, USA) at 37 °C and 5 % CO2.
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3

Culturing Human Meningioma Cell Lines

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The human benign meningioma cell line BEN-MEN-1 was obtained from Leibniz-Institute DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Braunschweig, Germany) and the human malignant meningioma cell line IOMM-Lee (ATCC ® CRL-3370™) was obtained from American Type Culture Collection (ATCC, Manassas, USA). Both cell lines were cultured in Dulbecco's P. Selke et al.: Glycation of meningioma cells modified Eagle's medium (DMEM) supplemented with 100 μg/mL of streptomycin, 100 U/mL of penicillin, 4 mM glutamine and 10% fetal bovine serum (FBS, Sigma Aldrich, St. Louis, MO, USA) at 37 °C in a 5% CO 2 incubator. The cell lines were split every 2-3 days with 0.1% Trypsin-ethylenediaminetetraacetic acid (EDTA) solution for 2 min.
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4

Culturing Meningioma Cell Lines

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The human benign meningioma cell line BEN-MEN-1 was obtained from Leibniz-Institute DSMZ (Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH, Braunschweig, Germany) and the human malignant meningioma cell line IOMM-Lee (ATCC® CRL-3370™) was obtained from American Type Culture Collection (ATCC, Manassas, VA, USA). Both cell lines were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM) supplemented with 100 µg/mL of streptomycin, 100 U/mL of penicillin, 4 mM of glutamine, and 10% fetal bovine serum (FBS, Sigma-Aldrich, St. Louis, MO, USA) at 37 °C in a 5% CO2 incubator. The cell lines were split every 2–3 days with 0.1% Trypsin-EDTA (Ethylenediaminetetraacetic acid) solution for 2 min.
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