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Pcdna3.1 ev

Manufactured by GenePharma
Sourced in China

PcDNA3.1 (EV) is a plasmid vector that can be used for the expression of proteins in mammalian cells. It contains a strong viral promoter, a multiple cloning site for the insertion of the gene of interest, and a selection marker for the identification of transfected cells.

Automatically generated - may contain errors

2 protocols using pcdna3.1 ev

1

STAT1 Overexpression in Liver Cancer Cells

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SMMC7721 and HepG2 cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10 % fetal calf serum at 37 °C and 5 % CO2. The plasmids of pcDNA3.1 (EV) and pcDNA3.1-STAT1 were obtained from GenePharma. pcDNA3.1 (EV) and pcDNA3.1-STAT1 were transfected into SMMC7721 and HepG2 cells at 70 % confluence using X-tremeGENE HP DNA transfection reagent (Roche, Mannheim, Germany) according to the manufacturer’s protocol. Cells were transfected for 48 h in 6-well plates and then analyzed for flow cytometry, MTT assay, western blot and qRT-PCR.
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2

Mcl-1 Overexpression and PTEN Silencing

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The empty vector (pcDNA3.1, EV) and pcDNA3.1-Mcl-1 (OV Mcl-1) were obtained from GenePharma (China). The myr-Akt vector was purchased from Addgene (USA). siRNA against PTEN (si-PTEN) and negative scramble control (si-NC) were purchased from RioBio Ltd. (China). The transfection was conducted using lipofectamine 2000 (Life Technologies, USA) according to the manufacturer's instructions. The transfection efficiency was evaluated using western blotting.
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