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Label IT® RNAi Delivery Controls

Fluorescently labeled RNAi duplexes ideal for In Vitro or In Vivo tracking

Product No.QuantityPriceAdd to Cart
Label IT® RNAi Delivery Control, Cy™3
MIR 790010 µg (0.75 nmol)$128.00
MIR 7901100 µg (7.5 nmol)$630.00
Label IT® RNAi Delivery Control, Fluorescein
MIR 790210 µg (0.75 nmol)$97.00
MIR 7903100 µg (7.5 nmol)$473.00
To inquire about bulk pricing, please call 888-530-0801.
International inquiries please call +1-608-441-2852.

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  • Sensitive - Easily visualize transfected cells and assess delivery efficiency using fluorescent microscopy.
  • Inert - Not known to target any mammalian genes or cause off-target effects.
  • Compatible - Suitable for co-delivery experiments with functional siRNA.
  • Ease of Use - Supplied as a ready to use 10 µM stock solution with a 10X RNAi Dilution Buffer.

Data


Label IT RNAi Controls Label IT RNAi Controls, Version 2
Figure 1A Figure 1B
The Label IT® RNAi Delivery Controls Allow Quick Assessment of Delivery Efficiency For In Vitro Applications.

Figure 1A. HeLa cells were transfected in serum-containing media with the Label IT® Cy™3 RNAi Delivery Control (red) using the TransIT-siQUEST®™ Transfection Reagent. Twenty-four hours post-transfection, the cells were fixed, then counterstained to locate the nuclei (blue) and the actin (green).

Figure 1B. HeLa cells were transfected in serum-containing media with the Label IT® Fluorescein RNAi Delivery Control (green) using the TransIT-TKO® Transfection Reagent. Twenty-four hours post-transfection, the cells were fixed, then counterstained to locate the nuclei (blue) and the actin (red).
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Figure 2:Visualization of the Label IT Cy™3 RNAi Delivery Control in Liver Sections Following Tail Vein Injection.
Figure 2. Visualization of the Label IT® Cy™3 RNAi Delivery Control in Liver Sections Following Tail Vein Injection. TransIT®-QR Hydrodynamic Delivery Solution was used to deliver 25 µg of Label IT® Cy™3 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).
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