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BioReagent,DNase, RNase free,PCR Reagent,Suitable for molecular biology,for DNA and RNA applications,10 μL/T BioReagent,DNase, RNase free,for DNA and RNA applications,PCR Reagent,Suitable for molecular biology for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Avoid repeated freezing and thawing Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
The StableMax RT-qPCR Master Mix (with Dye, UDG) is a one-tube, probe-based RT-qPCR premix optimized for both single and multiplex RNA detection. Its unique buffer system is compatible with Taq DNA polymerase and reverse transcriptase, enabling seamless reverse transcription and amplification in a single reaction.
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Key Features:
✔ Visual tracking: Yellow dye (non-inhibitory) confirms reagent addition, preventing omissions
✔ Contamination control: dUTP/UDG system eliminates carryover amplicon contamination
✔ Broad applications: Suitable for one-step RT-qPCR (RNA targets) and hot-start DNA amplification
✔ Optimized performance: High sensitivity and reproducibility for low-abundance targets
Reagent Preparation
Thaw all components at room temperature or 4°C.
Mix gently and centrifuge briefly before use.
Recommendations:
Protect probes from light.
Aliquot master mix to avoid freeze-thaw cycles.
Prepare Reaction Mix
| Component | Volume per 25 μL | Volume per 50 μL | Final Concentration |
| StableMax RT-PCR Master Mix (Dye, UDG, One Tube) | 10 μL | 20 μL | 1× |
| Primer-probe Mix | 1 μL | 2μL | / |
| Templates | 5 μL | 10 μL | / |
| ddH₂O | Up to 25 μL | Up to 50 μL | / |
| Total | 25 μL | 50 μL | / |
*Note:
Primer/template volumes can be adjusted.
For multiplex assays, optimize primer concentrations empirically.
Mixing:
Gently pipette mix or vortex briefly.
Centrifuge at room temperature to collect liquid.
PCR Amplification:
Load tubes onto a thermal cycler with heated lid (105°C recommended).
| Step | Temperature | Time | Cycles |
| 1 | 50℃ | 15min | 1 |
| 2 | 95℃ | 2min 30s | 1 |
| 3 | 94℃ | 10s | 45 |
| 4 | 55℃ | 40s(Fluorescence read) | 45 |
Optimization Guidelines:
a. Reverse Transcription: 5–15 min (adjust based on target abundance).
b. Cycle Number: Reduce to 40 cycles for high-copy targets.
c. Primer Design:
Final concentration: 0.2 μM (typical).
Tm ≥55°C (use software for accurate calculation).
Adjust annealing temperature (±3°C) if amplification is suboptimal.
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Mar 31, 2026 | FP1508907 | |
| Certificate of Analysis | Mar 31, 2026 | FP1508907 |
Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.
View Suitable for molecular biology grade guide → View BioReagent grade guide → View DNase, RNase free grade guide → View PCR Reagent grade guide → View for DNA and RNA applications grade guide →