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Mle 12

Manufactured by BNCC

The MLE-12 is a laboratory equipment product. It is designed for specific core functions within a laboratory setting. No further details are available to provide an unbiased and factual description while maintaining conciseness.

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2 protocols using mle 12

1

Sepsis model using MLE-12 cells

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The alveolar epithelial cell line MLE-12 was purchased from the BeNa Culture Collection; Beijing Beina Chunglian Institute of Biotechnology. Cells were cultured in DMEM/F12 Coon's medium (DMEM/F12; Thermo Fisher Scientific, Inc.) containing 10% FBS (Thermo Fisher Scientific, Inc.) and maintained in a 5% CO2 incubator at 37˚C. After the cells were passaged three times, cells in logarithmic phase were selected for follow-up assays.
The sepsis cell model was established using MLE-12 cells. Cells in the logarithmic phase were routinely cultured for 24 h at 37˚C. When the degree of cell fusion reached 90%, 100 ng/ml LPS (Sigma-Aldrich; Merck KGaA) was added to the culture for 24 h at 37˚C based on data from a previous study (18 (link)).
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2

Influenza A Virus Infection in Lung Epithelial Cells

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The mouse lung epithelial (MLE‐12) cell lines were purchased from the BeNa Culture Collection. Cells were cultured in Dulbecco's Modified Eagle Medium (DMEM) containing 10% (v/v) fetal bovine serum (FBS), in a humidified atmosphere of 95% air‐ 5% CO2 at 37°C. MLE‐12 cells were cultured in 6 well culture plate, and then the cells were transfected with miR‐205‐5p mimic, miR‐205‐5p inhibitor, miR‐431‐5p mimic, miR‐431‐5p inhibitor, NC or inhibitor negative control (INC), with lipofectamine 2000 for 48 h. miR‐205‐5p inhibitor, miR‐431‐5p inhibitor, INC were synthesized by Genepharma. These miRNA mimic (or respective inhibitor) transfected MLE‐12 cells were simultaneously infected with influenza A virus (MLE‐12 Infection model). The cells cultured in complete medium were considered as normal control. The culture plate was cultured in a 37°C, 5% CO2 incubator. The cells were harvested 48 h after transfection, and Western blot was carried out using the primary antibodies against NP (Abcam) and GAPDH (Cell Signalling) as an internal control.23
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