The largest database of trusted experimental protocols

5 protocols using mir 370 3p mimic

1

Regulation of KCNQ1OT1 by miR-370-3p

Check if the same lab product or an alternative is used in the 5 most similar protocols
Small interfering (si)-KCNQ1OT1, si-negative control (NC), miR-370-3p mimics, mimics-NC, miR-370-3p inhibitor, inhibitor-NC, pcDNA-FOXM1, and pcDNA-NC were purchased from RiboBio (Guangzhou, China). The above factors were transfected into WI-38 cells using Lipofectamine 3000 (Invitrogen, Carlsbad, CA, USA) for 48 h in accordance with the user guide.
+ Open protocol
+ Expand
2

Plasmid and microRNA transfection protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Overexpressed TUG1 plasmid (pcDNA-TUG1), TUG1 shRNA, control plasmid (pcDNA-NC), and control shRNA were constructed by GeneChem (Shanghai, China). miR-370-3p mimics, miRNA 370-3p inhibitors, and miRNA mimics control were purchased from RiboBio (Guangzhou, China). By applying LipofectamineTM 2000 (Invitrogen, Carlsbad, CA, US) according to the instructions, we transfected plasmid, shRNA or microRNA mimics into cells.
+ Open protocol
+ Expand
3

Modulating circITGA7 Expression

Check if the same lab product or an alternative is used in the 5 most similar protocols
To artificially upregulate or downregulate the expression of circITGA7, the pcD-ciR overexpression vector (circITGA7), empty vector (vector), small interfering RNA targeting circITGA7 (si-circITGA7), and negative control (si-NC) were purchased from GenePharma (Shanghai, China). miR-370-3p mimic and its corresponding negative control (mimic-NC) were purchased from RiboBio (Guangzhou, China). All the vectors were transfected into cells with Lipofectamine 3000 (Thermo Fisher Scientific, USA) following the manufacturer's instructions.
+ Open protocol
+ Expand
4

Breast Cancer Cell Line Cultivation

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human breast cancer cell lines (MCF-7, MDA-MB-453, MDA-MB-231, and HCC-1937) and a normal mammary epithelial cell line (HBL-100) were purchased from American Type Culture Collection (Manassas, VA, USA). All cells were cultured in Dulbecco’s modified Eagle’s medium (Gibco, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS, Gibco) and 1% penicillin/streptomycin (Invitrogen, Carlsbad, CA, USA) in a humidified atmosphere with 5% CO2 at 37 °C. Cells have been authenticated by STR profiling and tested for mycoplasma contamination. MiR-370-3p mimic, miR-370-3p inhibitor, their respective controls, small interfering RNA (siRNA) against FGF14 expression (si-FGF14), and negative control siRNA (si-NC) were chemically synthesized by RiboBio (Guangzhou, China). The FGF14-overexpressing plasmid pCMV3-FGF14-Flag and empty vector were from Sino Biological Inc. (Beijing, China). Cells were plated in 6-well plates at 60–70% confluence one day prior to transfection. Cell transfection was conducted using Lipofectamine 2000 (Invitrogen) in accordance with the manufacturer’s instructions. Table S2 lists the siRNA sequences.
+ Open protocol
+ Expand
5

Circulating ITGA7 Regulation

Check if the same lab product or an alternative is used in the 5 most similar protocols
To arti cially upregulate or downregulate the expression of circITGA7, the pcD-ciR overexpression vector (circITGA7), empty vector (vector), small interfering RNA targeting circITGA7 (si-circITGA7) and negative control (si-NC) were purchased from Genepharma (Shanghai, China). miR-370-3p mimic and its corresponding negative control (mimic-NC) were purchased from RiboBio (Guangzhou, China). All the vectors were transfected into cells with Lipofectamine 3000 (Thermo Fisher Scienti c, USA) following the manufacturer's instructions.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!