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Endothelial growth medium egm 2 mv

Manufactured by Lonza
Sourced in United States, Switzerland

Endothelial growth medium (EGM-2 MV) is a cell culture medium designed to support the growth and maintenance of endothelial cells. It contains a proprietary blend of growth factors, supplements, and other components optimized to provide a suitable environment for the proliferation and differentiation of endothelial cells in vitro.

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2 protocols using endothelial growth medium egm 2 mv

1

Isolation and Characterization of Endothelial Progenitor Cells

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G-CSF was provided by UBI pharma Inc. (Taipei, Taiwan). Fluorescein isothiocyanate (FITC) anti-mouse Sca-1 and phycoerythrin (PE) anti-mouse Flk-1 antibodies were purchased from eBioscience (San Diego, CA, USA). Isotype-identical antibodies were obtained from Becton Dickinson (Franklin Lakes, NJ, USA). The antibodies listed below were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA): rabbit anti-eNOS, anti-p-eNOS, mouse anti-VEGF, anti-α-SMA, and anti-β-actin. Rabbit antibodies for STAT3 and p-STAT3 were obtained from Cell Signaling Technology (Beverly, MA, USA). Mouse antibodies for IL-10 were purchased from Serotec (Oxford, UK). Rat anti-CD31 was obtained from BD Pharmingen (San Diego, CA, USA). Phenylmethylsulfonyl fluoride (PMSF) protease inhibitor, Histopaque-1077 (density: 1.077 g/mL), and 2,5-diphenyltetrazolium bromide (MTT) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Endothelial growth medium (EGM-2 MV) and growth factors for EPC culture were obtained from Lonza (Morristown, NJ, USA).
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2

Isolation and Culture of Murine ADSCs

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Murine ADSCs (mADSCs) were isolated from subcutaneous fat pads of female heterozygous Tie2CreERT2 carriers (3-4 months old). Briefly, fat was excised from the isoflurane-anesthetized animals (n = 3), minced, and digested with 2 mg/ml collagenase type 1 (Worthington Biochemical, Lakewood, NJ, USA) at 37°C. Digested tissue was centrifuged at 300 × g to separate floating adipocytes. Pellets containing the stromal vascular fraction were resuspended in Endothelial Basal Medium-2 (EBM2; Lonza, Bazel, Switzerland) with 5% fetal bovine serum (FBS; Lonza), filtered through a 100-µm nylon filter, and centrifuged again at 300 × g. Cells were resuspended in Endothelial Growth Medium EGM2-MV (Lonza), allowed to adhere to plastic, and propagated until the third passage (P3) at 37°C in a humidified atmosphere of 5% CO 2 and 95% O 2 . Before injection, cells were trypsinized (Lonza) and resuspended in EBM2 at a concentration of 3 × 10 6 cells/ml.
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