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Hek293t cell line

Manufactured by Shanghai Cell Bank
Sourced in China

The HEK293T cell line is a widely used human embryonic kidney cell line. It is derived from human embryonic kidney cells and is transformed by the addition of the SV40 large T antigen. HEK293T cells are commonly used in various research applications, including gene expression, protein production, and cell biology studies.

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5 protocols using hek293t cell line

1

Culturing Human Neuroblastoma, HEK293T, and HeLa Cells

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SH-SY5Y human neuroblastoma cells were grown in 1:1 mixture of MEM and F12, supplemented with 10% heat-inactivated fetal bovine serum (FBS), 1 mM sodium pyruvate, 0.1 mM nonessential amino acid, 1.5 g/L sodium bicarbonate, 100 units/mL penicillin, and 100 μg/mL streptomycin. All media and supplements were purchased from Gibco (Gaithersburg, MD, USA). Cells were maintained at 37 °C in a humidified atmosphere of 5% CO2. Cells were treated with D-mannose for the 12 h before RNA or 24 h before protein extraction.
HEK293T cell line was purchased from Shanghai Cell Bank of Chinese Academy of Sciences (GNHu17) and grown in DMEM medium (Gibco, 12100046) supplemented with 10% heat-inactivated fetal bovine serum (FBS; Gibco, 10099–141). Cells were all cultured in a humidified cell incubator with an atmosphere of 5% CO2 at 37 °C.
Hela cell line was purchased from ATCC (American Type Culture Collection) and grown in DMEM medium (Gibco, 12100046) supplemented with 10% heat-inactivated fetal bovine serum (FBS; Gibco, 10099–141). Cells were all cultured in a humidified cell incubator with an atmosphere of 5% CO2 at 37 °C.
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2

Cell Culture Protocols for HEK293T and Glioma

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The HEK293T cell line and human glioma cell lines were purchased from the Shanghai Cell Bank, Type Culture Collection Committee, Chinese Academy of Sciences. The cells were grown in DMEM supplemented with 10% fetal bovine serum (Gibco). All cell lines were cultured in a cell incubator with a 5% CO2 atmosphere under saturated humidity at 37 °C.
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3

Culturing Human Cancer Cell Lines

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SGC-7901 and MGC-803 human gastric cancer cell line, HEK-293T cell line, and human skin fibroblast HSF cell line were purchased from the Cell Bank of Shanghai (Shanghai, China) and cultured in Dulbecco minimum essential medium (DMEM), supplemented with 1% penicillin/streptomycin and 10% fetal bovine serum (Hyclone, Logan, UT, USA), at 37 °C in a humidified atmosphere with 5% CO2.
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4

Culturing Human Liver Cell Lines

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HCC cell lines, including the Hep3B, Huh7, HCCLM3, HepG2, Hep 1−6 and PLC5 cell lines and the HEK293T cell line, were purchased from Shanghai Cell Bank of the Chinese Academy of Science. The normal human hepatic cell line THLE‐3 was purchased from the American Type Culture Collection (ATCC). Cell line authentication was performed by the ATCC Human STR Profiling Cell Authentication Service. Hep3B cells were cultured in MEM (HyClone) supplemented with 10% fetal bovine serum (FBS) purchased from Gibco. The other cells were maintained in DMEM (HyClone) supplemented with 10% FBS (Gibco). All cells were cultured at 37°C in a 5% CO2 incubator.
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5

Cell Culture Protocols for Thyroid and Kidney Cell Lines

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Human normal thyroid cell line Nthy-ori 3-1; PTC cell line TPC-1, BCPAP and K1; human embryonic kidney 293T (HEK293T) cell line was purchased from Shanghai Cell Bank, Chinese Academy of Sciences. Nthy-ori 3-1, TPC-1, BCPAP cell lines were reared with RPMI-1640 complete medium (Meilunbio, Dalian, China), while 293T and K1 were reared in DMEM-H complete medium (Meilunbio, Dalian, China). All media contained 10% fetal bovine serum (FBS) (ExCell Bio, Shanghai, China) and 1% penicillin-streptomycin (Beyotime, Shanghai, China), and the cell culture conditions were 37 °C, 5% carbon dioxide.
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