Production of soluble CEACAM domains in human cells

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Revision as of 18:55, 15 February 2025 by ESO wikiadmin (talk | contribs) (Created page with "{| class="wikitable" |+ !Materials ! ! ! |- | |Plasmid DNA | | |- | |DMEM |Cell culture medium with L-glutamine and 4.5 g/l glucose (PAA Laboratories) | |- | |10% CS |calf serum (PAA Laboratories) | |- | |2xHBS |16.4 g NaCl, 11.9 g HEPES, 0.21 g Na<sub>2</sub>HPO4, solve in 1 l ddH<sub>2</sub>O, pH 7, sterile filtration | |- | |CaCl<sub>2</sub> solution |2.5 M CaCl<sub>2</sub> | |- | |OptiMEM |Serum-reduced medium with L-glutamine and HEPES (Gibco) | |} === Procedure =...")
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Materials
Plasmid DNA
DMEM Cell culture medium with L-glutamine and 4.5 g/l glucose (PAA Laboratories)
10% CS calf serum (PAA Laboratories)
2xHBS 16.4 g NaCl, 11.9 g HEPES, 0.21 g Na2HPO4, solve in 1 l ddH2O, pH 7, sterile filtration
CaCl2 solution 2.5 M CaCl2
OptiMEM Serum-reduced medium with L-glutamine and HEPES (Gibco)

Procedure


HEK293T-cells are transfected with 5 µg plasmid DNA, coding for N-terminal domains of different receptors. After 6-8 hours the DMEM-medium is replaced by 5ml serum-reduced OptiMEM-medium. Due to the lack of a transmembrane domain, the N-terminal domains are secreted into the medium. After three days, the medium is collected in a 50 ml tube and centrifuged for 15 min at 5000 rpm to remove cell fragments. The supernatants containing the soluble proteins are stored at -20°C.