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BioReagent,DNase, RNase free,PCR Reagent,Suitable for molecular biology,for DNA and RNA applications,1 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 StableLink RT-qPCR Kit (with UDG) is a two-component, probe-based RT-qPCR master mix comprising Buffer Mix and Enzyme Mix. It is designed for sensitive fluorescent quantitative PCR detection in single or multiplex RNA targets. Optimized for performance, the buffer system is uniquely formulated to support both Taq DNA polymerase and reverse transcriptase activity, ensuring broad target compatibility and exceptional reaction stability.
This kit incorporates a dUTP/thermolabile UDG carryover prevention system, enabling rapid degradation of uracil-containing contaminants at room temperature.
Applications: Qualitative/quantitative PCR, multiplex PCR.
Product Component Table
FP1509102 | Components | 100T | 1000T | 10000T | Storage |
FP1509102A | StableLink RT-PCR Buffer Mix | 1.25 mL | 10×1.25 mL | 125 mL | -20℃ |
FP1509102B | StableLink RT-PCR Enzyme Mix | 100 μL | 1.0 mL | 10 mL | -20℃ |
Protocol
Reaction Setup Preparation:
1. Thaw all required reagents at room temperature or 4°C. Mix thoroughly before use.
2. Prepare the PCR Reaction Mixture according to the table below:
| Component | Volume for 25 μL System | Final Concentration |
| StableLink RT-PCR Buffer Mix | 12.5 μL | 1× |
| StableLink RT-PCR Enzyme Mix | 1 μL | 1× |
| Primer/Probe Mix | 1 μL | / |
| Template | 5 μL | / |
| ddH₂O | To 25 μL | / |
| Total Volume | 25 μL |
Note:
"1x" indicates the working concentration of the enzyme mix as provided.
The amounts of primers, probes, and template can be adjusted according to experimental requirements.
Adjust the volumes of primers, probes, and template as needed for your specific assay; use RNase-Free ddH₂O to bring the reaction to the final volume.
To prepare reaction volumes other than 25 μL (e.g., 50 μL), scale the reagent volumes proportionally (e.g., double the volumes for a 50 μL reaction).
3. Mixing and Setup:
After preparing the reaction mixture, mix gently by pipetting or brief vortexing. Centrifuge briefly to collect the contents at the bottom of the tube. Proceed to PCR amplification.
Standard Thermal Cycling Protocol:
| Step | Temperature | Time | Circulation |
| 1 | 50℃ | 10min | 1 |
| 2 | 95℃ | 2min | 1 |
| 3 | 95℃ | 15s | 45 |
| 4 | 60℃ | 40s (Acquire Fluorescence) | 45 |
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 | Apr 01, 2026 | FP1509102 | |
| Certificate of Analysis | Apr 01, 2026 | FP1509102 |
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 →