pIEX-5-6His-mMBP-UMODpXR

Protein Expression Eukaryotic cells - HEK293 mMBP

Experiment
Protein Expression Eukaryotic cells - HEK293 mMBP
Product
pIEX-5-6His-mMBP-UMODpXR from Luca Jovine, Karolinska Institutet, Department of Biosciences an
Manufacturer
Luca Jovine, Karolinska Institutet, Department of Biosciences an

Protocol tips

Protocol tips
Transfection mixes were prepared by first combining serum-free medium and DNA, then adding PEI, and finally incubating the resulting solution for 10 min at 20 °C before adding it to the cells.

Publication protocol

"DNA for transfection was prepared using HiSpeed Plasmid Midi/Maxi kits or EndoFree Plasmid Giga kits (QIAGEN). Human embryonic kidney (HEK) 293T or 293S (ATCC CRL-3022) cells were amplified, transferred to a suitable expression vessel and transiently transfected using 25 kDa branched PEI, based on a published protocol (Aricescu et al., 2006). Fresh DMEM medium supplemented with 4 mM L-Gln (Thermo Fisher Scientific) and – if required – 2% fetal bovine serum (Biological Industries) was added to 90–95% confluent cells using the volumes specified in Table S1 for transfection of 6-well plates (10 cm2/well; Corning), T-flasks (150 cm2; BD Biosciences), ribbed roller bottles (2125 cm2; Greiner) or cell factories (2528 cm2; Thermo Fisher Scientific). Transfection mixes were prepared by first combining serum-free medium and DNA, then adding PEI, and finally incubating the resulting solution for 10 min at 20 °C before adding it to the cells. Unlike HEK293T cells, HEK293S cells tend to detach from ribbed roller bottles and were thus preferentially grown in T-flasks or cell factories. Medium was harvested three days after transfection.

For intracellular protein production, 200 ml FreeStyle 293-F HEK cells (HEK293F; Thermo Fisher Scientific) were grown in suspension in FreeStyle 293 Expression Medium (Thermo Fisher Scientific) in a 1.0 L plastic shake flask (Corning), using a shaking 8% CO2 incubator. When cells reached a density of 2.5–3.0 × 106 cells/ml, they were transiently transfected by diluting them 1:1 with medium containing 3.0 μg/ml plasmid DNA and 9.0 μg/ml 25 kDa branched PEI. Harvesting was performed four days after transfection."

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Manufacturer protocol

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