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The Human HeLa cell line is a widely used and well-characterized immortalized cell line derived from cervical cancer cells. It serves as a widely available and reproducible model for various cell biology and biomedical research applications.

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2 protocols using human hela

1

HeLa Cell Culture Protocol

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Human HeLa were obtained from the ATCC (American Type Culture Collection and were maintained in DMEM plus 10% FBS at 37°C under humidified conditions and 5% CO2.
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2

Establishment of Fto-deficient MEF Cells

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Wild-type MEF (mouse embryonic fibroblasts) and Fto−/− MEF cell lines were obtained from Prof. Arne Klungland. Spontaneously immortalized clonal MEF cell lines were established from individual E13.5-E15.5 days-old embryos obtained from heterozygous Fto+/− crossings. Limbs were removed and remaining tissue chopped into small pieces and homogenized into single-cell suspension using a pipette. MEFs are grown in DMEM with 10% serum, 2 mM glutamine and penicillin/streptomycin. Cells grown for 4–7 days were trypsinized and frozen in complete medium with 10% DMSO as stock. Cells are grown in complete medium for 2–4 days before using them for following analysis. Human HeLa, HepG2, HEK293T, Mel624, and 3T3-L1 cell lines were purchased from ATCC. The aforementioned cells were maintained in DMEM (Gibco, #11965) with 10% fetal bovine serum (FBS, Gibco, 10438–026) and 1× Pen/Strep (Gibco, 15140) at 37°C with 5% CO2. FTO stable knockdown and the knockdown control AML cells were obtained from Prof. Jianjun Chen and cultured as previously reported (Li et al., 2017 (link)).
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