Home Protocols Luna® Universal Probe One-Step RT-qPCR Kit Protocol (E3006)

Luna® Universal Probe One-Step RT-qPCR Kit Protocol (E3006)

  • Prepare RNA of interest using desired RNA extraction and purification methods. Determine concentration by OD260 absorbance.
  • Make dilutions of RNA to be used for the standard curve. These should be prepared fresh before each experiment and can be diluted in either water or TE.

Reaction Setup: For best results, we recommend running each RNA standard and sample in triplicate.

 COMPONENT  20 µl REACTION
  FINAL CONCENTRATION
 Luna Universal Probe One-Step Reaction Mix (2X)
  10 µl
  1X
 Luna WarmStart® RT Enzyme Mix (20X)
  1 µl
  1X
 Forward primer (10 µM)
  0.8 µl
  0.4 µM
 Reverse primer (10 µM)
  0.8 µl
  0.4 µM
 Probe (10 µM)
  0.4 µl
  0.2 µM
 Template RNA
  variable  < 1 µg (total RNA)
 Nuclease-free Water
  to 20 µl
  


  1. Thaw Luna Universal Probe One-Step Reaction Mix and other reaction components at room temperature, then place on ice. After thawing completely, briefly mix each component by inversion, pipetting or gentle vortexing.
  2. Determine the total volume for the appropriate number of reactions, plus 10% overage and prepare assay mix of all components except RNA template accordingly. Mix thoroughly but gently by pipetting or vortexing. Collect liquid to the bottom of the tube by brief centrifugation.
  3. Aliquot assay mix into qPCR tubes or plate. For best results, ensure accurate and consistent pipetting volumes and minimize bubbles.
  4. Add RNA template to qPCR tubes or plate. Seal tubes with flat, optically transparent caps; seal plates with optically transparent film. Care should be taken to properly seal plate edges and corners to prevent artifacts caused by evaporation.
  5. Spin tubes or plates briefly to remove bubbles and collect liquid (1 minute at 2,500–3,000 rpm).
  6. Program real-time instrument with indicated thermocycling protocol (see table below). Ensure a plate read is included at the end of the extension step.
   
Confirm selection of appropriate detection channel(s) for the fluorophore(s) present in the assay.
   
For faster results, the “Fast” ramp speed mode can be used where available (e.g., Applied Biosystems StepOnePlus®, QuantStudio®, 7500 Fast instruments).

 CYCLE STEP
 TEMPERATURE
 TIME  CYCLES
 Reverse Transcription
  55°C*  10 minutes
  1
 Initial Denaturation
  95°C  1 minute
  1
 Denaturation

 Extension		  95°C

 60°C		  10 seconds

 30 seconds**(+plate read)
 40-45
* A 55°C RT step temperature is optimal for Luna WarmStart Reverse Transcriptase. To ensure best performance and full WarmStart activation, avoid using a temperature of < 50°C.
** For Applied Biosystems real-time instruments use a 60 second extension step.