Liquid real-time PCR master mix for heat drying of qPCR assays
2.5 x conc. master mix
| Cat. No. | Amount | Price (EUR) | Buy / Note |
|---|---|---|---|
| PCR-180-1ML | 1 ml | 58,09 | Add to Basket/Quote Add to Notepad |
| PCR-180-10ML | 10 ml | 465,00 | Add to Basket/Quote Add to Notepad |
| PCR-180-100ML | 100 ml | Ask for Quotation |
For general laboratory use.
Please centrifuge briefly before opening (volume ≤2 ml).
Shipping: shipped on gel packs
Storage Conditions: store at -20 °C
storage at 4 °C for up to 1 week;
up to 10 freeze-thaw cycles without reduction in performance
Shelf Life: 12 months
Form: liquid
Concentration: 2.5x conc.
Description:
Liquid qPCR ProbesMaster for Drying is a liquid 2.5 x conc. master mix designed for custom-specific production of air-dried real-time PCR assays. It is optimized for using DNA probe based detection with Dual Labeled Fluorescent Probes, e.g. TaqMan®, Molecular Beacons or FRET probes.
The master mix contains all reagents required for qPCR (except template, primer and labeled fluorescent probe) in a well balanced composition. The high specificity and sensitivity of the mix is based on a hot-start polymerase with blocked activity at ambient temperature.
The mix can also be combined with ROX reference dye (#PCR-356) for use in qPCR instruments that require a ROX signal as an internal reference.
Content:
Liquid qPCR ProbesMaster for Drying
2.5 x conc. master mix containing antibody-blocked hot start polymerase, nucleotides, reaction buffer, additives and stabilizers
Preparation of the 2 x conc. master mix
Liquid qPCR ProbesMaster for Drying comes as 2.5 x conc. master mix and must be diluted to 2 x concentration prior to air drying. Drying of 10 μl, 2 x conc. master mix per well or assay to obtain a final assay volume of 20 μl is recommended. Designing of multiplex reactions with up to 4 primer-probe sets is possible but may require an additional effort for assay optimization.
Recommended concentrations of components:
| Comp. | final conc. |
| Liquid qPCR ProbesMaster for Drying | 2 x conc. |
| forward Primer 1 1) | 300 nM |
| reverse Primer 1 1) | 300 nM |
| Dual-Labeled probe 1 2) | 200 nM |
| forward Primer 2 1) | 300 nM |
| reverse Primer 2 1) | 300 nM |
| Dual-Labeled probe 2 2) | 200 nM |
| ROX Reference Dye (PCR-356) 3) | 500 nM |
| PCR-grade Water (PCR-258) | fill up to 2 x conc. |
1) The optimal concentration of each primer may vary from 100 to 500 nM.
2) Optimal results may require a titration of DNA probe concentration between 50 and 800 nM.
3) Optional if ROX Refernce Dye is required for the assay design and compatible with the used cycler. 500 nM is recommended for high ROX assays.
Dispensing the master mix
Vortex the 2 x conc. mix prepared above thoroughly to assure homogeneity. Dispense 10 μl to each PCR tube or well of the plate.
Air drying of the master mix
Use a drying oven or a climate chamber. For drying volumes of 10 μl per assay, we recommend drying at a temperature of 60 °C for 80 minutes.
However, this depends on the equipment used and the ambient humidity, and should be optimised for each production setup. Too high residual moisture content in the dried mixture may lead to faster degradation and thus to a reduced long-term stability of the product.
Addition of template DNA
To obtain a final assay volume of 20 μl, rehydrate the dryed qPCR mix in 20 μl template DNA or 20 μl PCR-grade Water for no-template controls and cap or seal the tube / plate. Do not exceed 10 ng DNA per reaction as final concentration. Tubes or plates should be centrifuged before cycling to remove bubbles.
Recommended cycling conditions:
| Initial denaturation and polymerase activation | 95 °C | 2 min | 1 x |
| Denaturation | 95 °C | 15 sec | 35-45 x |
| Annealing and Elongation | 60-65 °C 4) | 30 sec 5) | 35-45 x |
For optimal specificity and amplification an individual optimization of the recommended parameters, especially of the annealing temperature may be necessary for each new combination of template, primer pairs and DNA probe.
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