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Cellbind surface cell culture plates

Manufactured by Corning
Sourced in United States

CellBIND® Surface cell culture plates are a product line offered by Corning, a leading manufacturer of laboratory equipment. These plates are designed for cell culture applications, providing a specialized surface that supports the attachment and growth of various cell types.

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2 protocols using cellbind surface cell culture plates

1

Silencing USF1 in Liver Cell Lines

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The most effective USF1 silencing shRNA was screened in immortalized human hepatocytes (IHH). IHH were grown in William’s E medium (GIBCO-Life Technologies, Carlsbad, CA) containing 10% fetal bovine serum (FBS), 2 mM L-glutamine, 100 U/mL penicillin, 100 μg/mL streptomycin, 100 nM (20 mU/mL) insulin, and 50 nM dexamethasone (Sigma-Aldrich, St. Louis, MO) on CellBIND® Surface cell culture plates (Corning, Corning, NY). The human monocytic cell line, THP-1 and human hepatocellular carcinoma cell line, HuH-7 were cultured in RPMI (THP-1) or DMEM (HuH-7) medium supplemented with 10% fetal bovine serum and penicillin/streptomycin and to THP-1 media 25 mM HEPES was added. For transduction, 20,000 THP-1 cells seeded on 24-well plates or ~ 80% confluent HuH-7 cells in 12-well plates were treated for 24 h with SIGMA MISSION lentiviral preparations containing either the control shRNA expression vector (MISSION® pLKO.1-puro Non-Target shRNA) or the USF1 silencing shRNA expression vector (233475) at a MOI of ~ 1. Cells were selected with 6 μg/mL of puromycin for 14 days and were then used for cholesterol efflux assays.
Cell lines were found to be free of Mycoplasma contamination.
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2

Immunomodulation by rhBMP-2-primed Stem Cells

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Human ES-MSCs were provided by Daewoong Pharmaceutical Co., Ltd. ES-MSCs were cultured in a StemPro® MSC SFM XenoFree (Gibco, Waltham, MA, USA) supplemented with 1% L-glutamine (Gibco) and 1% penicillin/streptomycin on the Corning® CellBIND® surface cell culture plates (Corning Inc., Corning, NY, USA) at 37°C. For priming with rhBMP-2, cells were treated with rhBMP-2 (100 ng/ml) for 24 h. All experiments were performed using ES-MSCs at passage number 12. RAW264.7, murine macrophage cell line, was purchased from Korean Cell Line Bank (KCLB, Seoul, Korea). RAW264.7 cells were grown in RPMI-1640 medium at 37°C. To determine immunomodulation effect by paracrine factors from rhBMP-2-primed ES-MSCs in RAW264.7, cells were seeded in 60 mm culture dish at confluency 70%–80%. RAW264.7 cells were incubated with conditioned medium (CM) from ES-MSCs/rhBMP-2-primed ES-MSCs mixed with RPMI1640 (2:1 ratio). After 2 h, LPS was added for 6 h. Cells were lysed with RIPA buffer for western blotting analysis, and CM was used for ELISA.
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