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2 protocols using cwr 22rv1 22rv1

1

Cell Line Authentication and Culturing

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CWR-22RV1 (22RV1) and LNCaP cell lines were purchased from ATCC, authenticated every six months using short tandem repeat (STR) profiling, and frequently tested for mycoplasma contamination using the MycoAlert mycoplasma detection kit (Lonza). LNCaP95 cells were derived from LNCaP cells and cultured with 10% phenol red-free charcoal-stripped serum (CSS). 22RV1, LNCaP, and LNCaP-derived stable cell lines were generally cultured in RPMI-1640 medium with 10% FBS, which was replaced by the hormone-depleted medium (5% CSS) for 2–3 days before the subsequent assays.
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2

Prostate Cancer Cell Line Characterization

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Cell lines LNCaP (LNCaP-FGC, RRID:CVCL_1379), CWR22Rv1 (22Rv1, RRID:CVCL_1045), VCaP (RRID:CVCL_2235), DU145 (RRID:CVCL_0105), PC3 (RRID:CVCL_0035) and HEK293T (293T, RRID:CVCL_0063) were purchased from ATCC, PNT2 was purchased from Sigma–Aldrich (Cat# 95012613, RRID:CVCL_2164). All cell lines were cultured under conditions as recommended. C4-2B and C4-2B/EnzR cells were generous gifts from Dr. Allen C. Gao at UC Davis. Parental C4-2B cells were cultured in the RPMI-1640 medium supplemented with 10% FBS, while C4-2B/EnzR cells were maintained in the RPMI-1640 complete medium containing 10 μM enzalutamide. All cell lines were recently validated with STR analysis, and confirmed to be mycoplasma-free by Mycoplasma PCR Detection Kit (GeneCopoeia, Rockville, MD USA). Enzalutamide (Enz) was purchased from Selleck Chemicals (Houston, TX, USA).
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