EpiFectagen II
Cat. No. 0973, 250 transfections in 96-well plate
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Introduction
The delivery of foreign DNA into eukaryotic cells is one of the most common molecular biology techniques to study biological mechanisms. However, unlike transformed cell lines, the efficient transfection of primary cells can be a problem. EpiFectagen II is a cationic polymer-based transfection system specifically designed and optimized for efficient transfection of primary epithelial cells cultured in serum-free medium, such as Human Esophageal Epithelial Cells, Bronchial Epithelial Cells, Tracheal Epithelial Cells, Small Airway Epithelial Cells, Prostate Epithelial Cells, Corneal Epithelial Cells, Ovarian Surface Epithelial Cells and Mammary Epithelial Cells. Transfection with EpiFectagen II can be carried out in the presence of antibiotics. Instead of normal two-day transfection, an optimized one-day transfection procedure can be performed for time-saving and highly reproducible transfection.
Storage/Handling
Upon receipt, aliquot and store EpiFectagen II reagent A at -20°C, avoid repeated freezing/thawing cycles. Once thawed, store EpiFectagen II reagent A at 2-8°C and use in a month. EpiFectagen II reagent B can be kept at 2-8°C.
Quality Control
Each lot of EpiFectagen II is performance tested by transfecting Human Prostate Epithelial Cells (HPEpiCs, Cat. No. 4410, ScienCellT) with Promega® ?SV-bata-Galactosidase control vector. Gene expression is assayed by X-gal staining 24 hours post transfection. Typically, ~10% transfection efficiency can be achieved (Figure 1).
Procedures for Transfecting Adherent Cells in 96-well Plate*
Preparation of cells
On the day of transfection, coat 96-well plate with poly-l-lysine at 2 µg/cm2. Incubate at 37°C for 2-4 hours. Rinse the poly-l-lysine coated wells with sterile deionized H2O twice before seeding of cells. The pre-coating of poly-l-lysine ensures goodandeven epithelial cell adhesion.
Select a flask of epithelial cells with 60-80% confluency, harvest and dilute cells in culture medium to give a final concentration of ~1.1×105 cells/ml.
Transfection complex formation
Prepare plasmid DNA in sterile deionized H2O to give a final concentration of 1 µg/µl. To achieve successful transfection, high quality DNA with OD260/OD 280 of 1.8 or greater is recommended.
For each well, add 0.5 µl plasmid DNA, 12 µl sterile deionized H2O and 2 µl EpiFectagen II reagent B into a 1.5 ml sterile plastic tube. Vortex gently and spin down briefly. Then add 5.5 µl EpiFectagen II reagent A to make the total volume of the transfection mixture to be 20 µl, vortex for 5 seconds and spin down. Incubate at room temperature for 20-30 min.
Incubation of cells with transfection mixture
Plate 180 µl of cell suspension (~1.1×105 cells/ml) in each well to give ~2×104 cells per well.
Add 20 µl of transfection mixture to each well. Mix by gently rocking the plate side-to-side.
Culture the cells for ~ 24 hours under standard conditions. Or perform a medium change after 4-6 hours’ incubation with transfection mixtures, replace with 200 µl fresh culture medium, and culture for additional 16-18 hours. Generally longer incubation time with transfection mixture results in increased transfection efficiency and decreased cell viability.
Harvest cells 24 hours post transfection and assay for gene expression.
* The amounts of cells and various transfection reagents mentioned in the instruction are recommended for performing transfection in 96-well plate. For transfection in larger size wells, the amounts of cells and transfection reagents (DNA, sterile deionized H2O and EpiFectagen II reagents A&B) should be scaled up according to the surface area of the wells (Table 1).
Table 1. Recommended quantities of epithelial cells and EpiFectagen II reagents per well.
Culture Vessel
Growth Area (cm2/well)
# of cells
1 µg/µl DNA stock (µl)
Sterile DI H2O (µl)
EpiFectagen II reagent B (µl)
EpiFectagen II reagent A (µl)
Culture Medium (µl)
96-well plate
0.35
20,000
0.5
12
2
5.5
180
48-well plate
0.8
45,000
1.1
27
4.6
12.6
411
24well plate
2.0
115,000
2.9
69
11.6
31
1029
12-well plate
4.0
230,000
5.7
137
23
63
2057
6-well plate
9.6
550,000
13.7
329
55
151
4937
Click the picture for large image
Fig 1. HPFs expressing ß-galactosidase after transfection using FibroFectagen.