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Honokiol

Manufactured by Selleck Chemicals
Sourced in United States

Honokiol is a chemical compound found in the bark and leaves of Magnolia trees. It is a white crystalline solid that is commonly used in scientific research and laboratory settings. Honokiol's core function is to serve as a research tool, allowing scientists to study its potential biological and pharmacological properties.

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4 protocols using honokiol

1

Cell culture and drug treatment protocol

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H460, A549, H358, H2122, BEAS-2B, NIH3T3, CCD19-Lu cells were obtained from the American Type Culture Collection and cultured in an environment of 5% CO2 at 37°C in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS), CCD19-Lu cells were grown in MEM medium supplemented with 10% FBS, BEAS-2B cells were maintained in BEBM containing 0.01 mg/ml fibronectin, 0.03 mg/ml bovine collagen type I and 0.01 mg/ml bovine serum albumin. All cells were added 100 units/ml penicillin, and 100 μg/ml streptomycin. Honokiol was purchased from Selleck Chemicals. Antibodies to GAPDH, C-RAF, p-C-RAF, p-AKT (Ser473), p-ERK (Thr202/Thy204), P21, P27, Cyclin D1, Sirt3, Hif-1α, and ERK were purchased from cell signaling technology. Anti-AKT, KRAS antibody were acquired from Santa Cruz Biotechnology.
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2

Immunohistochemical Staining Protocol

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All chemicals and reagents were purchased from Sigma Chemical (St. Louis, Missouri, USA) unless otherwise stated. Honokiol was purchased from Selleck Chemical (Houston, Texas, USA). Antibodies used for immunohistochemical (IHC) were purchased from Abcam Inc. (Cambridge, Massachusetts, USA), or Aviva Systems Biology (San Diego, California, USA). Enzymes and reagents used for IHC staining were purchased from BioGenex (San Ramon, California, USA).
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3

Honokiol-Loaded MSNP Therapy for VSMCs

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VSMCs were obtained from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China). Honokiol was purchased from Selleck Chemicals (Houston, USA, catalog no. S2310), MSNPs (catalog no. 643645) and F‑127 pluronic gel were purchased from Sigma‑Aldrich Co. (St Louis, MO, USA). Transmission electron microscope was acquired from FEI (Hillsboro, Oregon, USA). FBS and 0.25% (w/v) trypsin−EDTA were obtained from Corning (New York, USA). DMEM and penicillin−streptomycin solution were purchased from Gibco (Thermo Fisher Scientific, Waltham, MA, USA). Culture flasks (25 cm2 surface area), culture plates, a filter of 8 μm pore size and confocal dishes were acquired from Corning Incorporated (Corning, NY, USA). 2F Fogarty embolectomy catheters were obtained from Edwards Lifesciences (Irvine, CA, USA). WST-1 was purchased from Beyotime Biotechnology (Shanghai, China). Foxp3/Transcription Factor Staining Buffer Set was purchased from Thermo Fisher Scientific. The primary antibodies used in Western blotting analysis were: anti-p-smad3, anti-p-ERK1/2 and anti-PCNA (Immunoway Biotechnology, NY, USA). α‑SMA antibody was obtained from Abcam (Cambridge, UK).
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4

Cell Line Cultivation and Treatment

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Human bronchial epithelial cell line (HBE) and human LUAD cell lines (H1299, A549, PC-9, Calu3) used in this study were procured from ATCC (Manassas, VA). They were grown with 10% FBS and 1% antibiotics in DMEM (Invitrogen, Carlsbad, CA) under 37 °C and 5% CO2. To treat PC-9 and Calu3 cells, 5 μg/ml of cycloheximide (CHX), 20 mmol/l of LiCl were available from Sigma-Aldrich (St. Louis, MO). A total of 20 mg/ml of MG132 and 100 μM of NSC 228155, 50 μM of Honokiol were purchased from Selleck Chemicals (Houston, TX). Totally, 10 nM of IGF-1 was bought from PeproTech (Rocky Hill, NJ). Totally, 10 nM of SAG was obtained from Abcam (Cambridge, MA).
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