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Mir 93 mimics

Manufactured by RiboBio
Sourced in China

MiR-93 mimics is a synthetic RNA molecule that mimics the function of the endogenous miR-93 microRNA. MicroRNAs are small, non-coding RNA molecules that play a role in regulating gene expression. The core function of MiR-93 mimics is to serve as a tool for studying the biological functions and target genes of miR-93 in various cellular and biological processes.

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3 protocols using mir 93 mimics

1

VSMC Isolation and Cell Culture

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Rat VSMCs were extracted from the aortas of six-week-old Sprague-Dawley male rats by using tissue adhesion methods. Blood vessels were cut out, and the fat, connective tissue and fibrous membrane were peeled off. The tissue was then cut into small pieces and transferred to a cell culture flask for overnight incubation with DMEM-F12 supplemented with 10% fetal bovine serum (FBS) in a humidified 5% CO2 atmosphere at 37 °C. Primary VSMCs between the 3rd and 6th passages were used for experiments. Human 293T cells were maintained in DMEM supplemented with 10% FBS in a humidified 5% CO2 atmosphere at 37 °C.
MiR-93 mimics, miR-93 inhibitors, antagomiR-93 and matched controls were purchased from RiboBio (Guangzhou, China). Mfn2 siRNA, Mfn2 pcDNA and matched controls were purchased from RiboBio (Guangzhou, China). Lipofectamine 2000 (Invitrogen, Waltham, MA, USA) was used to perform miRNA transfections according to the manufacturer's instructions. PDGF-BB (Sigma, St. Louis, MO, USA) was used in time and concentration gradient experiments to determine the final intervention dose.
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2

Investigating miR-93 and TIMP2 in Cells

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MiR-93 mimics, inhibitor, and negative control were obtained from Ribobio (Guangzhou, China.) The TIMP2 siRNA and negative control were purchased from Sigma Aldrich (St. Louis, MO, USA). Cells were seeded in six-well plates for 24 h, and then transfected with miR-93 mimic or its inhibitor, TIMP2 siRNA, or their scrambled negative control by using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) following the manufacturer’s protocol.
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3

Investigating miR-93 in RAW 264.7 Macrophages

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RAW 264.7 macrophages are widely used as a model of LPS-induced ALI, and play an essential role in the regulation of the inflammatory response (30 (link),31 (link)). Therefore, RAW 264.7 cells were selected for use in an ex vivo experiment as the present study focused on the ALI-induced inflammatory response. The RAW264.7 cell line was obtained from ATCC. The cells were maintained in DMEM supplemented with 10% FBS (Sigma-Aldrich; Merck KGaA), 1% penicillin and streptomycin (Sigma-Aldrich; Merck KGaA) at 37°C and a 5% CO2 incubator.
When the RAW264.7 cells in a 6-well plate grown to approximately 80% confluency, miR-93 mimics (20 nmol/l) and miR-93 inhibitor (20 nmol/l) were transfected into the cells at 37°C for 24 h, using Lipofectamine® 2000 (Invitrogen; Thermo Fisher Scientific, Inc.). miR-93 mimics, miR-93 inhibitor and the corresponding control vectors were purchased from RiboBio Co., Ltd.
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