Overview
Overview
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FluoMag-C corresponding to CombiMag (transfection reagent enhancer)
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FluoMag-P corresponding to PolyMag (DNA transfection reagent)
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FluoMag-S corresponding to SilenceMag (siRNA delivery)
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FluoMag-V corresponding to ViroMag (viral transduction)
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FluoMag-N corresponding to NeuroMag (neuron transfection)
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Easy cell labeling and tracking
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Non toxic
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Serum compatible
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This reagent needs to be used with a magnetic plate
| CATALOG NUMBER | UNIT SIZE |
| FN10100 |
FluoMag-N 100 µL |
| FC10100 |
FluoMag-C 100µL |
| FP10100 |
FluoMag-P 100µL |
| FS10100 |
FluoMag -S 100µL |
| FV10100 |
FluoMag-V 100µL |
Applications
RECOMMENDED FOR:
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Double labeling and co-localization studies using GFP or FITC labeled nucleic acids
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Transfection mechanisms follow (interaction with cells, intracellular pathway ...)
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Fluorescent resonance energy transfer (FRET) assay
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Analyze the association of vectors with the magnetic nanoparticles
Results
Figure 1: NIH-3T3 transfection with FluoMag-P and pEGFP plasmid DNA. NIH-3T3 cells (5x104 cells/well), growing on coverslips, were transfected in 24-well plates with 1 µg of pEGFP plasmid and 1µL of FluoMag-P per well as described in the Magnetofection instruction manual. At several times post-transfection, cells were fixed, stained with DAPI to detect nucleus (blue) and observed under a fluorescent microscope equipped with a CCD camera.
Figure 2: Transfection efficiency of FluoMag-S versus SilenceMag. GFP stably transfected MDCK and HeLa cells were plated the day before transfection in a 24-well plate. Cells were then treated with SilenceMag or FluoMag-S and siRNA (targeting GFP or targeting LacZ as control) as described in the SilenceMag instruction manual. Complexes were prepared with 1 μL of SilenceMag or FluoMag-S and 10nM (67.5ng) of siRNA. Cells were then transfected in 500 μL transfection volume. GFP expression level was monitored 72h post-transfection by detection of fluorescence intensity with a fluorometer.


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