Prostate Cancer Cell Line Characterization
Corresponding Organization : Flinders Medical Centre
Other organizations : Peter MacCallum Cancer Centre, University of Melbourne, Centre for Cancer Biology, University of South Australia, South Australia Pathology, Cancer Research UK, University of Cambridge, Monash University, South Australian Health and Medical Research Institute
Variable analysis
- Cell lines: LNCaP, VCaP, PC3, 22Rv1, C4-2B, LNCaP-V16D, LNCaP-MR49F, CWR-R1-D567, Luciferase-labelled RM1
- Not explicitly mentioned
- Cell culture media composition: RPMI1640 with 10% FBS and 2 mmol/L L-Glutamine (for LNCaP, C4-2B, 22Rv1, LNCaP-V16D)
- Cell culture media composition: RPMI1640 with 5% FBS and 2 mmol/L L-Glutamine (for PC3)
- Cell culture media composition: RPMI1640 with 10% FBS, 10 μmol/L enzalutamide, and 2 mmol/L L-Glutamine (for LNCaP-MR42D and LNCaP-MR49F)
- Cell culture media composition: RPMI1640 with 10% charcoal-stripped serum and 2 mmol/L L-Glutamine (for CWR-R1-D567)
- Cell culture media composition: DMEM (high glucose) with 10% FBS, 2 mmol/L L-Glutamine, 2 mmol/L sodium pyruvate, and 2 mmol/L of nonessential amino acids solution (for VCaP)
- Authentication by short tandem repeat profiling and regular screening for Mycoplasma contamination
- Not explicitly mentioned
- Not explicitly mentioned
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