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SYBR Green

Imagen ® Fast SYBR Green qPCR Premix

Cat. NO IPQ

 

Description

Imagen ® Fast SYBR Green qPCR Premix is a ready-to-use, 2X concentrated premix reagent including a novel Hotstart Taq DNA polymeraseSYBR®Green Ioptimized reaction buffer and nucleotides for running quantitative real-time PCR , including qPCR and 2-step qRT-PCR , in the SYBR®Green I detection format. Fast SYBR Green PCR Premix provides high sensitivitywide dynamic range and reproducibility , quantification.

 

 

 

Contents

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

 

Storage

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

http://si.secda.info/yb_md/wp-content/uploads/2017/07/20C-300x222.png

 

Reaction Mix Thawing and Handling

Imagen ® Fast SYBR Green 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 SYBR Green 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 SYBR Green qPCR Premix

12.5

1x

Forward Primer(10 uM)

0.625

200 - 500 nM

Reverse Primer(10 uM)

0.625

200 - 500 nM

DNA Template

2

100 ng - 1 pg

Nuclease-free water

9.25

-

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℃

60 sec

1

Amplification

 

Template denaturation

 

95℃

3 sec

35-40

 

Annealing / Extension and plate read

58 - 62℃

20 sec   © Data acquisition

Melt Curve

95℃

60℃

95℃

20 sec

30 sec

15 sec

1

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

  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.