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The T24 cell line is a well-characterized human bladder carcinoma cell line. It is derived from a transitional cell carcinoma of the urinary bladder. The T24 cell line is commonly used in cancer research to study the biology and behavior of bladder cancer cells.

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4 protocols using t24 cell line

1

Culturing Bladder Cancer T24 Cells

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Human bladder cancer T24 cell line, derived from a patient with bladder cancer (HLA-A1+), was obtained from China Center for Type Culture Collection (CCTCC). Cells were cultured in RPMI 1640 (HyClone) with 10% FBS (HyClone) and maintained at 37°C in a humidified atmosphere of 5% CO2.
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2

SEC23A Knockdown in Bladder Cancer T24 Cells

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The human bladder cancer T24 cell line was obtained from China Center for Type Culture Collection. T24 cells were cultured in MEM medium (Hyclone) with 10% fetal bovine serum (Gibco) and 1% penicillin-streptomycin (Hyclone) and maintained in 37°C with 5% CO2 incubator. The sequence for the sh-RNAs targeting SEC23A was 5′-GGAAGCTACAAGAATGGTTGT-3′. The lentivirus particles of shSEC23A were prepared by Sangon Biotech Co.
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3

Cell Lines and Culture Conditions

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Human bladder cancer T24 cell line was purchased from the China Center for Type Culture Collection (Wuhan University Collection Center, Wuhan, China). Human bladder cancer cell line EJ and human bladder immortalized epithelium cell line SV-HUC-1 were kindly provided by Associate Professor Huageng Liang, Department of Urology, Union Hospital of Tongji Medical College, Huazhong University of Science and Technology, China. Human normal liver cell line L02 was purchased from iCell Bioscience Inc. (Shanghai, China). Human embryonic kidney cell line HEK293T was obtained from American Type Culture Collection (ATCC). Human lung cancer A549, cervical cancer Hela, glioma cancer U87, breast cancer MCF-7 and MDA-MB-231, and prostate cancer PC-3 cell lines were obtained from the College of Life Science and Technology, Huazhong University of Science and Technology (Wuhan, China). T24, EJ, A549, MCF-7, and U87 cells were cultured in Eagle’s minimum essential medium (MEM) supplemented with 10% fetal bovine serum (FBS). L02, HEK293T, Hela, MDA-MB-231, and PC-3 cell lines were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS). SV-HUC-1 cells were grown in Ham’s F-12K medium supplemented with 10% FBS. All the cultures were maintained at 37°C in a humidified 5% CO2 incubator.
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4

Preparation and Use of Glycyrrhetinic Acid Solution

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The human bladder cancer T24 cell line was obtained from China Center for Type Culture Collection (CCTCC, No : GDC078). T24 cells were cultured in MEM medium (Gibco) with 10% FBS, 100 units/ml penicillin and 100 units/ml streptomycin, then maintained in 37°C with 5% CO2 incubator (Binder, Germany). Preparing GA stock solution at a concentration of 500 µg/ml: precisely weighed 2.00 mg GA in a EP tube, added 4 ml FBS free MEM medium, mixed with a vortex to ensure complete dissolution, and then stored at -20°C. The GA stock solution needs to be diluted before use. Specifically, the GA stock solution was taken out and dissolved in the dark at 37°C, and then it was diluted to the appointed concentration with FBS-free MEM medium to obtain the working solution. Attention should be paid here to avoid light in the use of GA.
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