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LCL721.221 cell line细胞株
BioVector NTCC质粒载体菌种细胞基因保藏中心
Cell line LCL721.221, EBV transfected B cell line, MHC class I A, B, C negative,MHC class II positive
Culture medium RPMI / 10% FCS
Transfection protocol:
Transfection with Plasmid pEGFP-N1 (in bidistilled H2O). (Example)
Electroporation buffer Eppendorf Hypoosmolar Electroporation Buffer (PH)
Cuvette Eppendorf, 2 mm gap width, 400 μl
Temperature RT (20-25 °C)
1. Harvest the cells in the exponential growth phase and centrifuge them (for 5 minutes, 200 x g, at room temperature).
2. Resuspend the cells in RPMI / 0.5% FCS, determine the number of cells and centrifuge them (for 5 minutes, 200 x g,
at room temperature). Remove supernatant.
3. Resuspend the cells in medium, set the cell number to 1 x 106 cells/ml and centrifuge them (for 5 minutes, 200 x g, at
room temperature). Remove supernatant.
Note: The overall incubation time in the Eppendorf Electroporation Buffer must not exceed 30 minutes to
guarantee a successful electroporation!
4. Resuspend the cells in Hypoosmolar Electroporation Buffer. Add and mix plasmid DNA (20 μg/ml final concentration,
in bidistilled H2O).
5. Transfer 400 μl cell suspension into electroporation cuvettes (2 mm gap width). The cell suspension must be free of
air bubbles.
6. Electroporation:
Mode Eukaryotes “¤“
Voltage (V) 200 V
Time constant (t) 40 μs
No. of pulses (n) 1
7. After the pulse, allow the cell suspension to stand in the cuvette for 15 minutes at room temperature.
8. Carefully transfer the cell suspension with a pasteur pipette from the cuvette into 3 ml RPMI /10% FCS, and cultivate
them in a 55 mm culture dish.
Detection methods for transfection:
The expression of the plasmid pEGFP-N1 by viable 721.221 cells can be detected after 24 hours with a flow cytometer
by costaining with propidium iodide (final concentration 1 μg/ml). Incubate for 10 min. at RT.
Result:
Survival rate: 86.18%
Transfection rate: 13.28% based on the number of surviving cells.
Results were measured 24 hours after transfection.
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