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2 protocols using karpas 422 cell line

1

Cell Line Acquisition and Use

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The Karpas 422 cell line was obtained from the Deutsche Sammlung von Mikroorganismen und Zellkulturen. The KAS-6/1 cell line was a gift from Dr. Diane Jelinek and described previously [26 (link)].
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2

Maintaining and Culturing Cell Lines

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The KARPAS-422 cell line was obtained from the Deutsche Sammlung von Mikroorganismen und Zellkulturen (DSMZ; Germany). Pfeiffer, Z-138, MDA-MB-468, and Toledo lines were obtained from the American Type Culture Collection (ATCC). KARPAS-422 and Pfeiffer cell lines were grown in RPMI-1640 medium (Gibco) with HEPES supplemented with 20% Fetal Bovine Serum (FBS; Sigma Aldrich), 1% Glutamax (Life Technologies), and 1% Sodium Pyruvate (Life Technologies) at 37 °C with 5% CO2. Toledo and MDA-MB-468 cells were cultured with RPMI-1640 medium supplemented with 10% FBS. Z-138 cells were cultured with IMDM medium (Gibco) supplemented with 10% horse serum (Gibco). Every 3–4 days, when the cell cultures reached approximately 70–90% confluence, cells were split by dilution with fresh media. Cell culture density was determined using a Vi-Cell Analyzer (Beckman Coulter). For experimental assays, cells were plated to maintain subconfluence for the duration of the assay and maintained at 37 °C with 5% CO2 for a minimum of 16 h prior to compound dosing.
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