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Taqman

Imagen ® TaqMan RT-qPCR Premix

Cat. No 

 

Description

Imagen ® TaqMan RT-qPCR Premix uses a designed fluorogenic probe to detect target PCR products during real-time PCR cycle, fluorescent is detectable when the quencher of probe is removed during the PCR extension cycle. Real-time TaqMan RT-PCR kit complete reverse transcription and TaqMan Real-time PCR in a single tube. Components necessary for performing TaqMan Real-time PCR from RNA template are specially prepared to ensure high specificity and high sensitivity.

 

 

 

Contents

The Imagen ® TaqMan RT-qPCR Premix is supplied as a ready-to-use 2x reaction mix. The formulation contains, Hotstart Taq DNA polymerase, Reverse transcriptases, dNTPs, MgCl2, reaction enhancers, and stabilizers.

 

Storage

  • -20 °C
  • Protected from light
  • Avoid repeated freezing and throwing

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Reaction Mix Thawing and Handling

Imagen ® TaqMan RT-qPCR Premix is delivered in a 2x ready-to-use format. To use the mix, thaw the vial on ice to 4 °C.

 

Please completely mix the vial and briefly centrifuge to ensure all components are at the bottom of the tube. Store on ice protected from light until ready to use. If using automated liquid handling, let sit at ambient temperature for 10 min to further reduce the viscosity.

Application

  • TaqMan RT-qPCR based on Specific Probes.
  • Detection and Quantification of RNA targets.
  • High Throughput Applications.

 

Prepare the qPCR Reaction Mix

  1. Mix the Imagen ® TaqMan RT-qPCR Premix thoroughly but gently until it’s completely homogenous.
  2. Prepare the qPCR Reaction Mix for the number of reactions required as shown in table below and plus 10% overage.

Reagent

Volume (ul)

Final conc.

Imagen ® TaqMan RT-qPCR Premix

12.5

1x

Forward Primer(10 uM)

0.75

300 - 600 nM

Reverse Primer(10 uM)

0.75

300 - 600 nM

Fluorogenic Probe(10 uM)

0.5

200-400 nM

RNA Template

2

100 ng - 10 pg

Nuclease-free water

8.5

-

Final volume

25

-

 

 

 

 

 

 

 

 

 

 

 

  1. Vortex the tube to mix the contents thoroughly, then centrifuge briefly to collect the contents at the bottom of the tube. (*Use good pipetting practice to ensure assay precision and accuracy of dispensing.)
  1. Add DNA (and nuclease-free water, if needed) to the PCR tubes or wells containing the reaction mix, seal tubes or wells with flat caps or optically transparent film, and gently vortex to ensure thorough mixing of the reaction components.
  2. Program the thermal cycling protocol on the real-time PCR instrument.

Step

Temp.

Time

Cycles

 

Reverse Transcription

48

30 min

1

 

DNA polymerase activation and template denaturation

Amplification

95

10 min

1

 
 

Amplification

Template denaturation

95

20 sec

35-40

 
 

Annealing / Extension and plate read

58 - 62

60 sec   © Data acquisition

 
 

 

 

 

 

 

 

 

 

 

 

 

 

 

  1. Load the PCR tubes or plates onto the real-time PCR instrument and start the qPCR run program.
  2. When thermal cycling is complete, perform data according to the instructions in the instrument-specific software.