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Penicillin streptomycin amphotericin b solution

Manufactured by Corning
Sourced in United States

Penicillin/streptomycin/amphotericin B solution is a sterile, liquid mixture of antibiotics and an antifungal agent commonly used in cell culture applications. The solution contains defined concentrations of penicillin, streptomycin, and amphotericin B to prevent bacterial and fungal contamination in cultured cells.

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2 protocols using penicillin streptomycin amphotericin b solution

1

Docetaxel Nanoparticle Formulation and Cell Lines

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Docetaxel was purchased from ScinoPharm Taiwan (Tainan, Taiwan). Soybean lecithin (S 100) was provided by Lipoid (Ludwigshafen, Germany). 1.2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000] (DSPE-PEG2000) and 1.2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000] (DSPE-PEG5000) were purchased from NOF (Tokyo, Japan). Kolliphor® TPGS was obtained from BASF (Florham Park, NJ, USA). 3.30-Dioctadecyloxacarbocyanine perchlorate (DIO) was obtained from Sigma-Aldrich (St. Louis, MO, USA). Tynen® (docetaxel), a generic product, was provided by TYY Pharmaceutical (Taipei, Taiwan). Fetal bovine serum, non-essential amino acids and sodium pyruvate were obtained from Thermo Fisher Scientific (Waltham, MA, USA). Dulbecco’s Modified Eagle Medium (DMEM), Minimum Essential Medium (MEM) and penicillin/streptomycin/amphotericin B solution were purchased from Corning Incorporated (Corning, NY, USA). Other reagents and solvents were of analytical grade. WS1, MIA PaCa-2 and HT-29 were supplied by American Type Culture Collection (Manassas, VA, USA). WS1/FAP cells were human WS1 fibroblasts engineered to overexpress human FAP by lentiviral infection.
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2

Lymphocyte Isolation and Immortalization

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Blood obtained from patients DGDP289A, DGDP289B and other family members (Figure 1A) was used to isolate lymphocytes by density gradient centrifugation. From patient’s whole blood samples, lymphocytes were isolated using density gradient centrifugation. Ten mL of the blood sample was layered on top of the 5 mL of Lymphocyte Separation Medium (Cellgro, Manassas, VA, USA) in 15 mL tubes, and the tubes were centrifuged at 400× g for 30 min. From the tubes, the lymphocyte layer in the middle was carefully removed and washed in PBS (Fisher, Pittsburgh, PA, USA) twice at 300× g for 10 min. Then, the lymphocytes were immortalized by adding cyclosporine A (Sigma, St. Louis, MO, USA) and Epstein–Barr virus (EBV) to the cell pellet, and maintained in RPMI (Hyclone, South Logan, Australia) containing 20% fetal bovine serum (Atlas Biologicals, Fort Collins, CO, USA), 1% l-glutamine (Corning, Corning, NY, USA), and 1% penicillin/streptomycin/amphotericin B solution (Corning, Corning, NY, USA) [26 (link)].
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