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Bovine growth serum bgs

Manufactured by Thermo Fisher Scientific
Sourced in Germany

Bovine growth serum (BGS) is a cell culture medium supplement derived from the blood serum of bovine (cattle) sources. Its core function is to provide a source of growth factors, nutrients, and other components necessary for the growth and maintenance of cells in in vitro cell culture applications.

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3 protocols using bovine growth serum bgs

1

Fibroblast Culture of Healthy and PARK6 Patients

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Human fibroblasts of 7 healthy controls and 3 PARK6 patients [17 (link)] (passage 8–12) were cultured in Dulbecco’s Modified Eagle Medium 4.5 g/L glucose (Invitrogen) plus 15% bovine growth serum (BGS, Thermo Scientific), 1% glutamine, 1% penicillin/streptomycin (all Invitrogen) at 37 °C and 5% CO2 in a humidified incubator.
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2

Isolation and Cryopreservation of Mouse Embryonic Fibroblasts

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The mice used were bred at the Central Animal Facility (ZFE) of the Goethe University Medical Faculty in Frankfurt, under FELASA-certified conditions, in accordance with the ETS123 (European Convention for the Protection of Vertebrate Animals), the Council Directive of 24 November 1986 (86/609/EWG) with Annex II and the German Animal Welfare Act. Approval of the local institutional review board (Regierungspraesidium Darmstadt, project V54-19c20/15-FK/1083) was given on 27 March 2017. MEF were prepared from individual embryos at 14.5 days post-coitus of WT and Pink1−/− mice, which were generated and bred as previously reported [20 (link)]. In brief, embryos were dissected from the uterus, extremities, and inner organs were removed and the tissue was treated with 0.05% trypsin (Gibco, Thermo Scientific, Schwerte, Germany) for 10–15 min. Cells were cultivated in Dulbecco’s Modified Eagle Medium 4.5 g/L glucose (Invitrogen, Karlsruhe, Germany) plus 15% bovine growth serum (BGS, Thermo Scientific), 1% glutamine, 1% penicillin/streptomycin (all Invitrogen,) at 37 °C and 5% CO2 in a humidified incubator, then Pink1−/− cells and their respective littermate WT controls were frozen in liquid nitrogen.
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3

Culturing and Characterizing HPV-Positive Cells

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Human foreskin keratinocytes (HFKs) were collected from neonatal foreskin tissue as described previously (Ruesch et al., 1998 (link)) and were maintained in Dermalife keratinocyte growth media (KGM; Lifeline). HPV31 positive CIN612 9E cells were grown in E-media supplemented with 5ng/mL mouse epidermal growth factor (BD Biosciences) and co-cultured mitomycin C treated J2 3T3 fibroblasts, as described previously (Wilson and Laimins, 2005 (link)). Organotypic raft cultures were derived from HFKs and CIN612 cells as previously described (Anacker and Moody, 2012 ). Generation and maintenance of HFKs retrovirally transduced with pLXSN-HPV31 E6, pLXSN-31 E7, and pLXSN-31 E6/E7 in combination has been previously described (Hebner et al., 2006 (link)). Prior to harvesting DNA, protein or RNA, fibroblast feeder cells were removed from HPV positive cells using Versene (1 mM EDTA in phosphate-buffered saline). 293T cells were grown Dulbecco’s modified Eagle’s medium (DMEM; Life Technologies) supplemented with 10% bovine growth serum (BGS; ThermoFisher Scientific).
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