T24 bladder cancer cells

Manufactured by American Type Culture Collection

The T24 bladder cancer cells are a well-characterized human urothelial carcinoma cell line. They are derived from the transitional cell carcinoma of the urinary bladder and are commonly used in cancer research.

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Lab products found in correlation

Mccoy s 5a modified medium, by American Type Culture Collection (2 mentions) Fetal bovine serum (fbs), by American Type Culture Collection (2 mentions) Glutamine, by Thermo Fisher Scientific (1 mentions) Dmem and rpmi 1640 cell culture media, by Thermo Fisher Scientific (1 mentions) Rpmi 1640 cell culture media, by Thermo Fisher Scientific (1 mentions) Lncap, by American Type Culture Collection (1 mentions)

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T24 cells (17 citations)

2 protocols using t24 bladder cancer cells

Prostate and Bladder Cancer Cell Culture

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VCaP, LNCaP, and NCI‐H660 prostate cancer cells, T24 bladder cancer cells, McCoy's 5 A Modified Medium, and fetal bovine serum (FBS) were purchased from ATCC (Manassas, VA). DMEM and RPMI‐1640 cell culture media and glutamine were purchased from Life technologies (Carlsband, CA). VCaP cells were maintained in DMEM supplemented with 10% FBS. LNCaP cells were maintained in RPMI‐1640 supplemented with 10% FBS, 2.8 mM l‐glutamine. NCI‐H660 cells were maintained in RPMI‐1640 medium supplemented with 5% FBS, 4 mM l‐glutamine, 0.005 mg/ml insulin, 0.01 mg/ml transferrin, 30 nM sodium selenite, 10 nM β‐estradiol, and 10 nM hydrocortisone. T24 bladder cancer cells were maintained in McCoy's 5 A Modified Medium, supplemented with 5% FBS. All cells were cultured in a 5% CO₂ humidified incubator at 37°C.

Nickens K.P., Ali A., Scoggin T., Tan S., Ravindranath L., McLeod D.G., Dobi A., Tacha D., Sesterhenn I.A., Srivastava S, & Petrovics G. (2015). Prostate cancer marker panel with single cell sensitivity in urine. The Prostate, 75(9), 969-975.

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Culturing and Maintaining Prostate and Bladder Cancer Cell Lines

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VCaP, LNCaP, NCI-H660 prostate cancer cells, T24 bladder cancer cells, McCoy's 5A Modified Medium and fetal bovine serum (FBS) were purchased from ATCC (Manassas, VA). DMEM and RPMI-1640 cell culture media and glutamine were purchased from Life technologies (Carlsband, CA). VCaP cells were maintained in DMEM supplemented with 10% FBS. LNCaP cells were maintained in RPMI-1640 supplemented with 10% FBS, 2.8 mM L-glutamine. NCIH660 cells were maintained in RPMI-1640 medium supplemented with 5% FBS, 4 mM L-glutamine, 0.005 mg/mL insulin, 0.01 mg/mL transferrin, 30 nM sodium selenite, 10 nM beta-estradiol, and 10 nM hydrocortisone. T24 bladder cancer cells were maintained in McCoy's 5A Modified Medium, supplemented with 5% FBS. All cells were cultured in a 5% CO₂ humidified incubator at 37°C.

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