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Taqman

Imagen ® Fast TaqMan qPCR Premix

Cat. No 

 

Description

Imagen ® Fast TaqMan qPCR Premix is a ready-to-use, 2X concentrated premix  including a novel Hotstart Taq DNA polymeraseoptimized reaction buffer and nucleotides with Rox reference dye and combines accurate using sequence-specific fluorogenic probe chemistries including hydrolysis probes (ex. TaqManMolecular beacon,etc…) which provides good specificity and amplification efficiency for real-time PCR.

 

 

Contents

The Imagen ® Fast TaqMan qPCR Premix is supplied as a ready-to-use 2x reaction mix. The formulation contains, Fast Hotstart Taq DNA polymerase, 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 ® Fast TaqMan 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

  • Quantitative real-time PCR
  • Quantitative 2-step RT-PCR
  • Gene expression analysis
  • Low copy gene detection

 

 

Prepare the qPCR Reaction Mix

  1. Mix the Imagen ® Fast TaqMan 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 ® Fast TaqMan 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

DNA 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

 

DNA polymerase activation and template denaturation

Amplification

95

1 min

1

 
 

Amplification

Template denaturation

95

3 sec

35-40

 
 

Annealing / Extension and plate read

58 - 65

10 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.