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High glucose dmem

Manufactured by ScienCell
Sourced in China, United States

High-glucose DMEM is a cell culture medium formulated with a high concentration of glucose (4.5 g/L) to support the growth and maintenance of a variety of cell types. It provides essential nutrients, vitamins, and amino acids necessary for cell proliferation and metabolism.

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2 protocols using high glucose dmem

1

Aptamer-Mediated Targeted Delivery of Lipid Nanoparticles

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DSPC (Avanti Corporation, USA), DSPE-PEG2000 (Avanti Corporation, USA), DSPE-PEG2000-maleimide (Avanti Company, USA), DC-cholesterol∙HCl (Avanti Company, USA), DPPE (Avanti Company, USA), glycerol (Sigma, USA), sodium hyaluronate (HA, 200–400 kDa, Xi’an Ruixi), aptamer PM1 base sequence SH-CCCCTGCAGGTGATTTTGCTCAAGTCGTTCCCGTCCTCTCCTCTGCGCCCCGTCTCGGCCAGTATCGCTAATCAGGCGGAT-HS, (Shanghai Shenggong, China), a sequence with FITC-labelled or unlabelled at the 5ʹ end, ANM33 and ANM33 double-modified with cy3 and amino groups (Guangzhou Ruibo, China), DiI fluorescent dye (Yeasen, USA), RAW264.7-T1 macrophages (Procell Life Science & Technology, China), oxidized low-density lipoprotein (ox-LDL; Yiyuan Biotechnology, China), Oil red O staining kit (Sigma, China), high-glucose DMEM (ScienCell, China), and double antibodies (ScienCell, USA) were used. A fluorescence microscope (LEICA CTR6000, Germany), laser confocal microscope (Leica SP8, Germany), flow cytometer (Beckman, USA), and laser nanoparticle size and zeta potential analyser (Malvern, UK) were also used.
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2

Endothelial-Macrophage Interplay in Ox-LDL Exposure

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Human umbilical vein endothelial HUVEC-T1 cells (Procell Life Science & Technology, China), RAW264.7-T1 Mφ (Procell Life Science & Technology, China), oxidized low-density lipoprotein (ox-LDL; Yiyuan Biotechnology, China), tumor necrosis factor-α (TNF-α; Bioss, China), and Transwell chambers (Corning, USA) were used. FITC-labelled anti-human CD44 flow cytometry antibody (Proteintech, USA), high-glucose DMEM (ScienCell, China), CCK-8 kit (Tongren Chemical, Japan), fetal bovine serum (FBS; ScienCell, USA, Israel), and double antibody (Gibco, USA) were purchased for this study. Endothelial cell basal medium (ECM; ScienCell, USA), FBS (ScienCell, USA), endothelial cell growth factor (ScienCell, USA), double antibodies (ScienCell, USA), and Fluorescence microscope (LEICA CTR6000, Germany); laser confocal microscope (Leica SP8, Germany); flow cytometer (Beckman, USA); laser nanoparticle size potential analyzer (Malvern, UK) were used.
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