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Mir 203 mimic

Manufactured by RiboBio
Sourced in China

The MiR-203 mimic is a synthetic RNA molecule designed to mimic the function of the natural microRNA MiR-203. MicroRNAs are small, non-coding RNA molecules that play a role in gene expression regulation. The MiR-203 mimic is intended for use in research applications to study the biological functions and effects of MiR-203 in various cellular and molecular processes.

Automatically generated - may contain errors

3 protocols using mir 203 mimic

1

c-Met Inhibitor BPI-9016M Protocol

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BPI-9016M, which is a selective small-molecular c-Met inhibitor, was kindly provided by Better Pharmaceuticals (Zhejiang, China). BPI-9016M was dissolved in 0.5% carboxymethylcellulose sodium (CMC) for PDX treatment. For other experiments, the drug was dissolved in dimethyl sulfoxide at a stock concentration of 50 mM and stored at -80 °C. The DKK1 siRNA, miR103 mimic, miR203 mimic, miR103 inhibitor and miR203 inhibitor were constructed by RiboBio (Guangzhou, China) and the pENTER-DKK1 plasmid was purchased from Vigenebio (Maryland, USA). The transfections were performed according to the protocol provided by the manufacturer (Lipo3000, Thermo Fisher, MA, USA).
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2

miR-203 Mimic Transfection Protocol

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miR-203 mimic and negative control (scramble) were obtained from RIBOBIO (Guangzhou, China). Cells were transfected with miR-203 mimic or scramble by Lipofectamine 2000 (Invitrogen) following to the manufacturer’s instructions.
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3

miR-203 Transfection Protocol in Human Intestinal Epithelial Cells

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HIECs was transfected with miR-203 mimic, miR-203 AMOs and negative control respectively (RiboBio). The transfection reagents was added into Opti-MEM (31985070, Invitrogen) serum-free medium (100 nM) and transfected into HIECs using X-treme reagent (4476115001, Sigma). Cells were harvested 48 h after transfection to extract total RNA or protein. Transfection reagents and X-treme were separately mixed with 25 μL of Opti-MEM. Then blend the two mixtures and incubate for 20 min at room temperature. The mixture was added to the cells and incubated at 37°C for 5 h. Oligonucleotides for transfection are shown in Table S1.
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