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Hsa mirna mimics

Manufactured by RiboBio
Sourced in China

Hsa-miRNA mimics are synthetic molecules designed to mimic the structure and function of human microRNAs (miRNAs). miRNAs are small, non-coding RNAs that play a crucial role in regulating gene expression. The Hsa-miRNA mimics provided by RiboBio are intended to be used as research tools for studying miRNA-mediated biological processes.

Automatically generated - may contain errors

3 protocols using hsa mirna mimics

1

Transfecting miRNA and siRNA into Gallbladder Cancer Cells

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Hsa‐miRNA mimics, hsa‐miRNA inhibitors, and their cognate control RNAs were purchased from RioBio (Guangzhou, China). The PLGF siRNA, c‐MYC siRNA, and si‐NC were purchased from Biotend (Shanghai, China). The miRNA mimics, miRNA inhibitors, and siRNA were transfected into NOZ or GBC‐SD cells using Lipofectamine 2000 transfection reagent (Invitrogen). Total RNA and protein were collected 48 hours after transfection. The siRNA sequences used are listed in Table S2.
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2

Regulation of ZFX Expression by miRNA

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Hsa-miRNA mimics and their cognate control RNAs were purchased from Ribobio (Guangzhou, China). Full-length ZFX cDNA (GenBank accession number NM_001178084.1) was cloned into a GV143 expression vector (Genechem, Shanghai, China). An empty vector was used as a control. Transfection was performed using Lipofectamine 2000 transfection reagent (Invitrogen) according to the manufacturer's instructions. Typically, a 50 nmol/L concentration of miRNA mimics was used for transfection of the RNA oligonucleotides. For plasmid transfections, 3 μg of DNA was used in a 6-well plate, and G418 (200 μg/mL) was added 24 h after transfection. For rescue experiments, 1 μg of plasmid was used in a 6-well plate. The sequences of the miRNAs used are listed in Supplementary Table S1.
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3

Transfecting miRNA Mimics and Inhibitors

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Hsa-miRNA mimics, hsa-miRNA inhibitors and their cognate control RNAs were purchased from Riobio (Guangzhou, China). Lentivirus-miR-143-3p and lentivirus-miR-NC were purchased from Genomeditech (Shanghai, China). Additionally, an ITGA6 overexpression plasmid was used for the rescue experiments. The miRNA mimics, miRNA inhibitors and plasmids were transfected into NOZ and GBC-SD cells using Lipofectamine 2000 transfection reagent (Invitrogen, USA). Total RNA and protein were collected 48 h after transfection.
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