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Complete endothelial cell growth media egm

Manufactured by PromoCell
Sourced in Germany

Complete Endothelial Cell Growth Media (EGM) is a cell culture medium specifically formulated to support the growth and maintenance of endothelial cells. It provides the necessary growth factors, vitamins, and other essential nutrients required for the optimal proliferation and differentiation of endothelial cells in vitro.

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2 protocols using complete endothelial cell growth media egm

1

Co-culture of HUVEC and HBMSC

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HUVEC׳s were purchased from PromoCell (Germany) and were used between passages 3 and 5. Cells were cultured in Complete Endothelial Cell Growth Media (EGM) (PromoCell, Germany), supplemented with 10% FCS (FirstLink,UK) and 1% Penicillin/Streptomycin (Gibco,UK). HBMSCs were obtained from patients at the RNOH undergoing total hip replacements (with informed consent and ethical approval) and were isolated based on the method by Igarashi et al. [20] (link). Cells were cultured in low glucose Dulbecco׳s Modified Eagles Medium (DMEM, Sigma USA) supplemented with 20% FCS and 1% Penicillin/Streptomycin. Cells were detached from tissue culture flasks, following washes with Phosphate Buffered Saline (PBS), and incubation with 0.5% trypsin at 37 °C for 5 min.
HUVEC׳s were pre-tested by PromoCell for cell proliferation and morphology. These were also positive for EC specific markers such as CD31 and von Willebrand Factor. HBMSCs were CD31 negative cells, with mesenchymal cell characteristics and differentiation potential into osteoblasts, chondrocytes and adipocytes.
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2

Culturing Human Umbilical Vein Endothelial and Rat Schwann Cells

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Human umbilical vein endothelial cells (HUVECs; PromoCell) were grown in complete Endothelial Cell Growth Media (EGM) (PromoCell). They were used between passages 4 and 10. Schwann cells were from the rat Schwann cell line SCL4.1/F7 (Health Protection Agency) and were grown in culture medium (Dulbecco's Modified Eagle's Medium , DMEM; Gibco). They were used between passages 4 and 20. All media were supplemented with 10% v/v heat-inactivated foetal bovine serum (FBS; Thermo Fisher Scientific) and 1% v/v Penicillin/Streptomycin (Gibco) and replaced every 2 days. All cell cultures and subsequent experiments were maintained in a humidified incubator with 5% CO 2 /95% air at 37 ºC.
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