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Sf 900 2 serum free media

Manufactured by Thermo Fisher Scientific

The SF-900 II serum free media is a cell culture medium formulated for the growth and maintenance of insect cells. It is designed to support the production of recombinant proteins and viral vectors without the need for supplementation with animal-derived serum.

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4 protocols using sf 900 2 serum free media

1

H5 Hemagglutinin Protein Expression in Insect Cells

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SF9 insect cells were grown in SF-900 II serum free media (Life Technologies). The cells were co-transfected with a pAcGP67 plasmid containing a H5 HA (A/Vietnam/1203/04 (H5N1), BEI Resources) expression construct and BD BaculoGold linearized baculovirus DNA (BD Biosciences). The H5 HA protein construct has an altered C-terminus, where the transmembrane and cytosolic regions of the protein were removed and replaced with an artificial trimerization domain (the foldon from T4 fibritin), and a His-tag as previously described (Stevens et al. 2006 (link)). Cell handling, transfection and protein expression were performed as recommended by the BD BaculoGold starter package kit (BD Biosciences). Viral titers were monitored using the BacPAK qPCR Titration Kit (Clontech Laboratories). For expression, fresh SF9 cells at 80% confluency were infected with H5 HA containing baculovirus solution at MOI between 3 and 6. 4 days later the suspension was collected and the cells were removed by centrifugation. H5 HA is secreted into the insect cell media and purified by Ni-affinity chromatography. The protein concentrate was then subjected to Sephacryl S300 gel filtration column with phosphate buffer (50 mM sodium phosphate/pH 8.1 and 50 mM NaCl) as a running buffer. Protein fractions were pooled and concentrated and the final yield was ~4 mg of H5 HA per liter of insect cell culture.
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2

Production and Purification of Recombinant H5 HA Protein

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SF9 insect cells were grown in SF-900 II serum free media (Life Technologies). The cells were co-transfected with a pAcGP67 plasmid containing a H5 HA (A/Vietnam/1203/04 (H5N1), BEI Resources) expression construct and BD BaculoGold linearized baculovirus DNA (BD Biosciences). The H5 HA protein construct has an altered C-terminus, where the transmembrane and cytosolic regions of the protein were removed and replaced with an artificial trimerization domain (the foldon from T4 fibritin), and a His-tag as previously described (Stevens et al. 2006 (link)). Cell handling, transfection and protein expression were performed as recommended by the BD BaculoGold starter package kit (BD Biosciences). Viral titers were monitored using the BacPAK™ qPCR Titration Kit (Clontech Laboratories). For expression, fresh SF9 cells at 80 % confluency were infected with H5 HA containing baculovirus solution at MOI between 3 and 6. 4 days later the suspension was collected and the cells were removed by centrifugation. H5 HA is secreted into the insect cell media and purified by Ni-affinity chromatography. The protein concentrate was then subjected to Sephacryl S300 gel filtration column with phosphate buffer (50 mM sodium phosphate/pH 8.1 and 50 mM NaCl) as a running buffer. Protein fractions were pooled and concentrated and the final yield was ~4 mg of H5 HA per liter of insect cell culture.
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3

BSEP Inhibition Assay in Sf9 Cells

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Spodoptera frugiperda 9 (Sf9) cells were obtained from the Tissue Culture Facility at the University of North Carolina-Chapel Hill. Cell culture media (Sf-900 II Serum Free Media) and TaqMan® genotyping supplies (including assay and master mix), were purchased from Thermo Fisher Scientific (Waltham, MA). BSEP antibody for immunoblot analysis was purchased from Abcam (ab140616; Cambridge, MA) and anti-rabbit IgG secondary antibody was purchased from Jackson ImmunoResearch (West Grove, PA). [14C]-Glycocholic acid (46.3 mCi/mmol; >97% radiochemical purity) and [3H]-taurocholic acid (9.74 Ci/mmol; >97% radiochemical purity) were purchased from Perkin Elmer (Waltham, MA). Compounds tested for inhibition studies were purchased from either Fisher Scientific (Thermo Fisher Scientific; Waltham, MA) or Sigma-Aldrich (St. Louis, MO). The scintillation cocktail, Bio-Safe II Complete Counting Cocktail, was purchased from Research Products International (Mt. Prospect, IL).
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4

Recombinant Baculovirus Expression of PDE3A and SLFN12

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The PCR products including PDE3A and SLFN12 were ligated into pFastBac-HT A to generate pFastBac-His-PDE3A and pFastBac-Flag-SLFN12 constructs. Then DH10Bac competent cells were transformed with the plasmid to prepare the recombinant bacmid according to the instruction for the Bac-to-Bac Baculovirus Expression System (Thermo Fisher). The Sf21 cells were transfected with the recombinant bacmid containing pFastBac-His-PDE3A and pFastBac-Flag-SLFN12 using CellfectinÒ Reagent (Thermo Fisher) in SF-900II serum-free media (Thermo Fisher). Log-phase Sf21 cells (8 3 10 5 cells/ml) in SF-900II serum-free media were infected with the medium containing recombinant baculovirus for 5 days, the cells were collected by centrifugation and the cell pellet was washed with cold PBS buffer and kept at À80 C until purification.
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