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Complete iscove s modified dulbecco s medium

Manufactured by Merck Group
Sourced in Germany

Iscove's Modified Dulbecco's Medium is a cell culture medium used to support the growth and maintenance of a variety of cell types. It provides the necessary nutrients and supplements for optimal cell proliferation and survival. The medium is a modification of the original Dulbecco's Modified Eagle's Medium, with additional components to enhance its versatility and performance in cell culture applications.

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2 protocols using complete iscove s modified dulbecco s medium

1

Primary human T cell isolation protocol

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Human embryonic kidney (HEK293T) cells and human hepatoma (HepG2) cells were purchased from ATCC (Manassas,VA), and human fibrosarcoma HT1080 cells were obtained from DSMZ (Braunschweig, Germany). All cells were grown in Dulbecco’s Modified Eagle’s Medium supplemented with penicillin (100 U/mL), streptomycin (100 μg/mL), 2 mM glutamine (all from Gibco/BRL, Karlsruhe, Germany), and 10% heat-inactivated fetal bovine serum (PAN, Aidenbach, Germany) at 37°C in a humidified atmosphere with 5% CO2.
Primary human T lymphocytes from peripheral blood (PB) samples from healthy adult volunteers who provided written informed consent that is documented in the department of Otorhinolaryngology & head/neck surgery (ENT). This study including the documentation was approved by the ethics committee of the Heinrich-Heine-University of Düsseldorf (ethics No. 4687). After Ficoll-Hypaque density gradient centrifugation, outgrowth of >95% T cells was achieved by incubation of the mononuclear cells on immobilized CD3 and CD28 antibodies (BD Bioscience, San Jose, CA) in combination with IL-2 (100 IU/ml, Chiron, Marburg, Germany) in complete Iscove’s Modified Dulbecco’s Medium (Sigma-Aldrich, Deisenhofen, Germany) as described previously [28 (link), 35 (link), 36 (link)].
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2

Cell Culture of Genetically Modified Lines

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Cell lines were obtained from the American Type Culture Collection. HEK-293T cells were cultured in complete Iscove’s modified Dulbecco’s medium (Sigma Aldrich) supplemented with 10% FCS and 2 mM Glutamax (Gibco) (cIMDM). RAJI and NALM6 were maintained in complete RPMI medium (Sigma Aldrich) supplemented with 10% FCS and 2 mM Glutamax (Gibco) (cRPMI). RAJI CD19 wild type (RAJI-19WT) cells were transduced with SFG vector for enhanced green fluorescence protein (eGFP) (RAJI-19GFP), and RAJI CD19 knockout (RAJI-19KO) cells were edited using CRISPR-Cas9. NALM6 FLUC cells were transduced with SFG vector to express firefly luciferin and a lipid anchored hemagglutinin (HA-GPI) tag.
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