One-Step qHDA (Real-time quantitative tHDA)
The following protocol is intended for real-time detection using the Applied Biosystems 7300 Real-Time PCR System.
The kit also can be coupled with real-time detection methods to conduct realtime quantitative tHDA (qHDA) and RT-HDA (qRT-HDA) to monitor amplification as it progresses. For optimal performance, use EvaGreen as a reporter dye and ROX as a passive reference dye. Sequence-specific probes can also be designed for qHDA experiments.
- Set up a 50 μl reaction in a MicroAmp optical tube (Applied BioSystems) in a sterile hood or a PCR Workstation.
H2O X μl 10X Annealing buffer II 5 μl MgSO4 (100 mM)* 2 μl NaCl (500 mM)* 4 μl IsoAmp® dNTP Solution 3.5 μl DNA template X μl Forward Primer (5 μM)* 0.75 μl Reverse Primer (5 μM)* 0.75 μl IsoAmp® Enzyme Mix 3.5 μl EvaGreen (20X, Biotium) 0.5 μl ROX Reference Dye (50X, Invitrogen) 1 μl Total volume 50 μl
- Mix the reaction by brief vortexing or by pipetting followed by brief centrifugation. Overlay the reaction mixture with 50 μl min eral oil. Place the tubes on ice.
- Real-time detection is carried out on a 7300 Real-Time PCR System (ABI) with the following well inspector setting: reporter dye: SYBR; quencher: none; passive reference dye: ROX. Use the following program:
Stage 1: (60 X)
Step1: 66ºC for 0:05
Step2: 65ºC for 1:55
Data collection and real-time analysis enabled
Stage 2: (1 X)
Dissociation Stage (default settings of the machine)
Melt curve data collection and analysis enabled
* The condition of tHDA reactions can be further optimized by titering thefollowing components:
Components Recommended concentration Recommended concentration for titering MgSO4 3.5 to 4 mM 3 to 4.5 mM NaCl 30 to 40 mM 20 to 50 mM Primer 75 to 100 nM 50 to 200 nM ProtoScript II RT (NEB M0368S) 1 to 2 units 0.5 to 10.5 units