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Pcdna e2f3

Manufactured by GenePharma
Sourced in China

PcDNA-E2F3 is a plasmid vector that contains the E2F3 gene. E2F3 is a member of the E2F family of transcription factors, which play a key role in the regulation of cell cycle progression. The PcDNA-E2F3 vector can be used for the expression of the E2F3 gene in various cell types.

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5 protocols using pcdna e2f3

1

miR-195-5p Regulation of E2F3 in AMC-HN-8 Cells

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miR-195-5p mimic and the negative control miRNA (miRNA-NC) were obtained from Guangzhou RiboBio Co., Ltd. The E2F3 overexpression vector pcDNA-E2F3 and empty control vector pcDNA-NC were constructed by Shanghai GenePharma Co., Ltd. The sequences were as follows: miR-195-5p mimic sense, 5'-UAGCAGCACAGAAAUAUUGGC-3'; miR-195-5p mimic antisense, 5'-CAAUAUUUCUGUGCUGCUAUU-3'; mimics negative control (miR-NC) sense, 5'-UUCUCCGAACGUGUCACGUTT-3'; miR-NC antisense, 5'-ACGUGACACGUUCGGAGAATT-3'. Cells were plated into 6-well plates (1x106 cells per well), and transfection was performed when cells at the logarithmic growth phase reached 80% confluence. According to the product instructions, AMC-HN-8 cells were transfected with miR-195-5p mimic (50 nM), miR-NC (50 nM), pcDNA-E2F3 (100 nM) and pcDNA-NC (100 nM) using Lipofectamine® 2000 (Invitrogen; Thermo Fisher Scientific, Inc.). The transfection efficiencies were assessed by RT-qPCR at 48 h after transfection.
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2

Gastric Cancer Cell Line Transfection

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The gastric cancer cell lines (SGC-7901, SUN-16, MKN-45, and AGS cells) and the human gastric epithelial cell line GES-1 (American Type Culture Collection, USA) were used in this study. All cells cultured respectively in Dulbecco's Modi ed Eagle Medium (DMEM, Gibco, USA) supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin and 100 μg/mL streptomycin (Hyclone, USA) and incubated in a 5% carbon oxide (CO 2 ) incubator at 37°C. For cell transfection, cells in logarithmic growth phase were transfected with corresponding constructs when the con uence was up to 80% following the instructions of Lipofectamine2000 (Invitrogen, USA).
The culture medium was replaced 6 hours later. H19-small interfering RNA (si-H19), miR-194 mimic, miR-194 inhibitor, pcDNA-E2F3, and negative control (NC) were constructed by Gene Pharma (Shanghai, China).
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3

Gastric Cancer Cell Transfection Protocol

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The gastric cancer cell lines (SGC-7901, SUN-16, MKN-45, and AGS cells) and the human gastric epithelial cell line GES-1 (American Type Culture Collection, USA) were used in this study. All cells cultured respectively in Dulbecco's Modi ed Eagle Medium (DMEM, Gibco, USA) supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin and 100 μg/mL streptomycin (Hyclone, USA) and incubated in a 5% carbon oxide (CO 2 ) incubator at 37°C. For cell transfection, cells in the logarithmic growth phase were transfected with corresponding constructs when the con uence was up to 80% following the instructions of Lipofectamine2000 (Invitrogen, USA). The culture medium was replaced 6 hours later. H19-small interfering RNA (si-H19), miR-194 mimic, miR-194 inhibitor, pcDNA-E2F3, and negative control (NC) were constructed by Gene Pharma (Shanghai, China).
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4

Gastric Cancer Cell Line Transfection

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The gastric cancer cell lines (SGC-7901, SUN-16, MKN-45, and AGS cells) and the human gastric epithelial cell line GES-1 (American Type Culture Collection, USA) were used in this study. All cells cultured respectively in Dulbecco's Modified Eagle Medium (DMEM, Gibco, USA) supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin and 100 μg/mL streptomycin (Hyclone, USA) and incubated in a 5% carbon oxide (CO 2 ) incubator at 37°C.
For cell transfection, cells in the logarithmic growth phase were transfected with corresponding constructs when the confluence was up to 80% following the instructions of Lipofectamine2000 (Invitrogen, USA). The culture medium was replaced 6 hours later. H19-small interfering RNA (si-H19), miR-194 mimic, miR-194 inhibitor, pcDNA-E2F3, and negative control (NC) were constructed by Gene Pharma (Shanghai, China).
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5

Gastric Cancer Cell Transfection Protocol

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The gastric cancer cell lines (SGC-7901, SUN-16, MKN-45, and AGS cells) and the human gastric epithelial cell line GES-1 (American Type Culture Collection, USA) were used in this study. All cells cultured respectively in Dulbecco's Modi ed Eagle Medium (DMEM, Gibco, USA) supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin and 100 μg/mL streptomycin (Hyclone, USA) and incubated in a 5% carbon oxide (CO 2 ) incubator at 37°C. For cell transfection, cells in the logarithmic growth phase were transfected with corresponding constructs when the con uence was up to 80% following the instructions of Lipofectamine2000 (Invitrogen, USA). The culture medium was replaced 6 hours later. H19-small interfering RNA (si-H19), miR-194 mimic, miR-194 inhibitor, pcDNA-E2F3, and negative control (NC) were constructed by Gene Pharma (Shanghai, China).
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