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in vitro and in vivo¿¡ Àû¿ë °¡´ÉÇÏ´Ù.
Fluorophore |
Excitation Wavelength (nm) |
Emission Wavelength (nm) |
Cy¢ç3 |
549 |
570 |
Fluorescein |
495 |
518 |
Label IT RNAi Delivery Control Àû¿ë
The Label IT¢ç RNAi Delivery Controls Allow Quick Assessment of Delivery Efficiency For In Vitro Applications.
Figure 1. HeLa cells were transfected in serum-containing media with (A) Label IT¢ç Cy¢ç3 RNAi Delivery Control (red) using the TransIT-siQUEST¢ç Transfection Reagent and (B) Label IT¢ç Fluorescein RNAi Delivery Control (green) using the TransIT-TKO¢ç Transfection Reagent. Twenty-four hours post-transfection, the cells were fixed, then counterstained to locate the nuclei (blue) and the actin (green).
Visualization of the Label IT¢ç Cy¢ç3 RNAi Delivery Control in Liver Sections Following Tail Vein Injection.
Figure 2. TransIT¢ç-QR Hydrodynamic Delivery Solution was used to deliver 25 ¥ìg of Label IT¢ç Cy¢ç3 RNAi Delivery Control (red) to a mouse using hydrodynamic delivery via the tail vein. Forty-five minutes post-injection the liver was harvested. Sections were processed to stain the nuclei (blue) and to stain the actin (green).
Label IT Plasmid Delivery Control Àû¿ë
The Label IT¢ç Cy¢ç3 Plasmid Delivery Control Allows Quick Assessment of Delivery Efficiency.
Figure 3. HeLa cells were transfected in serum-containing media with the
Label IT¢ç Cy¢ç3 Plasmid Delivery Control (red) using the TransIT¢ç-LT1 Transfection Reagent. Twenty-four hours post-transfection,
the cells were fixed, then counterstained to locate the nuclei (blue) and to stain the actin (green).
Visualization of Label IT¢ç Fluorescein Plasmid Delivery Control in Liver Sections Following Tail Vein Injection.
Figure 4. TransIT¢ç-QR Hydrodynamic Delivery Solution was used to deliver 25 ¥ìg of Label IT¢ç Fluorescein Plasmid Control (green) to a mouse using hydrodynamic delivery via the tail vein. One hour post-injection the liver was harvested. Sections were fixed to stain the nuclei (blue) and the actin (red).
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