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The HEK293T line is a human embryonic kidney cell line derived from human embryonic kidney cells. It is commonly used in cell biology research and biotechnology applications due to its ability to efficiently express recombinant proteins. The HEK293T line is a widely used and well-characterized cell line.

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4 protocols using hek293t line

1

Overexpression of CFAP52 in HEK293T Cells

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FLAG- and/or Myc-tagged pCMV vectors were used to construct expression plasmids. Mouse CFAP52 cDNA was produced by Sangon Biotech (Shanghai, China) and mouse testis cDNA template was used to amplify other genes by PCR. The primers for PCR amplification are listed in Figure 6—source data 1. Lipofectamine 3000 transfection reagent (Invitrogen, USA) was used to transfect HEK293T cells (from ATCC) and cycloheximide (MedChemExpress, Shanghai, China) was added to culture to block protein synthesis. HEK293T line was obtained from ATCC (American Type Culture Collection) and authenticated using STR profiling test by Shanghai Biowing Applied Biotechnology Co., Ltd.
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2

Cell Culture Protocols for HEK293T and 58 Cells

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The HEK293T line was purchased from ATCC and used at a passage number below 15. The cells were cultured in DMEM (Sigma-Aldrich) with 10% heat-inactivated bovine serum, and 1% penicillin-streptomycin-glutamine (100x, Gibco), from here on referred to as complete DMEM (cDMEM). The 58 alpha-beta- TCR negative cell line [26 (link)], from here on referred to as 58 ​cells, was a gift from Dr. Bernard Malissen (Centre d’Immunologie de Marseille Luminy, France). The 58 ​cell line was cultured in RPMI-1640 (Sigma-Aldrich) with 10% heat-inactivated bovine serum, and 1% penicillin-streptomycin-glutamine (100x, Gibco), from here on referred to as complete RPMI (cRPMI). For activation assays with 58 ​cells, 2mM Ca2+ was typically added to the medium. Cells were incubated in a humidified incubator with 5% CO2 at 37 ​°C and handled in laminar flow hoods using standard sterile techniques.
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3

Cell Culture Protocol for WiT49 and HEK293T

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WiT49 cells were a gift from Dr. Sharon Plon's laboratory. The HEK293T line was obtained from American Type Culture Collection. Both lines were maintained in Dulbecco's modified Eagle medium supplemented with 10% fetal bovine serum (FBS) and 1× antibiotic antimycotic (Gibco, 15240096) and cultured at 37°C with 5% CO2.
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4

Diverse Pancreatic Cancer Cell Lines

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Pa01C, Pa02C, Pa04C, Pa14C and Pa16C cell lines were provided by A. Maitra (MD Anderson Cancer Center). The remaining PDAC cell lines and HEK-293T line were obtained from American Type Culture Collection (ATCC) and were maintained in either DMEM or RPMI 1640 supplemented with 10% FBS. Cell lines 12282, 14837 and 192 were derived from the doxycycline-inducible iKRAS mouse model3 (link) and cultured in RPMI 1640 supplemented with 10% FBS. The RIE-1 cell line was received from R. Coffey (Vanderbilt University) and cultured in RPMI 1640 supplemented with 10% FBS. All cell lines were maintained in a humidified chamber with 5% CO2 at 37 °C. Organoids were cultured at 37 °C in 5% CO2. Cells were seeded in growth factor–reduced Matrigel (Corning) domes and fed with complete human feeding medium: advanced DMEM/F12-based WRN condition medium (L-WRN, ATCC CRL-3276), 1× B27 supplement, 10 mM HEPES, 0.01 µM GlutaMAX, 10 mM nicotinamide, 1.25 mM N-acetylcysteine, 50 ng ml–1 hEGF, 100 ng ml–1 hFGF10, 0.01 µM hGastrin I, 500 nM A83–01, 1 µM PGE2 and 10.5 µM Y27632. All cell lines were regularly monitored for mycoplasma contamination and immediately discarded if a positive result was detected. All cell line identities were verified by short-tandem-repeat profiling.
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