Features:
- Excellent Multiplex Master for assays of 4 and more
targets.
- Hotstart Taq with mAB and all components for succesfull
multitarget PCR
- Setting up at roomtemperature; optimized for block based
instruments
- 2-times concentrated; 2x1,25 ml Mastermix
Available mixtures:
- NO-ROX (product code: M100-200; M100-1000)
- LOW-ROX (product Code: M110-200, M110-1000)
- HIGH-ROX: (product code: M120-200, M120-1000)
Applications:
- Detection and quantification of DNA and cDNA targets
- Profiling gene expression
- Microbial detection
- Viral load determination
Compatibility:
Block based PCR-Cycler
Description:
The PCR-Master Mix contains all reagents required for qPCR (except template and primer) in a premixed 2x concentrated ready-to-use solution.
The high specificity and sensitivity of the mix is achieved by an optimized hot-start polymerase.
Its activity is blocked at ambient temperature and switched on automatically at the onset of the initial denaturation. The thermal activation prevents the extension of non-specifically annealed
primers and primer-dimer formations at low temperatures during PCR setup.
The mix offer dUTP instead of dTTP.
Concentration: The Mastermix is 2x concentrated
List of components qPCR / MultiplexMaster mix:
Hot-Start Polymerase for qPCR, dATP, dCTP, dGTP, dUTP, ROX (depending on the product-code), optimized reaction buffer with
KCl, Ammoniumsulfate and MgCl2, stabilizers and enhancers,
separate Tube: PCR-grade water
Transportation: with blue ice
Storage: @ 4°C up to 3 months; @ -20°C for more than 12 months,
Note: protect from Light when ROX is used
Components (50 µl) | Volume per reaction | final conc. |
2X qPCR / MultiplexMaster |
25 µl | 1x |
Up-stream primer (10 µM stock) |
1,5 µl (range: 0,5-2.5 µl) | 300 nM |
Down-stream primer (10µM stock) |
1,5 µl (range: 0.5-2,5 µl | 300 nM |
Template DNA |
X µl (0.1-15 ng/ml plasmid DNA) (1-10 µg/ml genomic DNA) |
< 500ng DNA |
Sterile dest. Water |
up to 50 µl total reaction volume |
- vortex all solutions carefully before using and before PCR
- may you add the enzyme mix after Template DNA
- an individual optimization of annealing temperature may be
necessary for new combinations of primers and Template DNA
General Thermo-Cycler protocol for qPCR / RTD-PCR Master mix:
Note: working with EvaGreen just select the optical setting for FAM or SYBR Green at the cycler
Step | Time | Temperature |
Initial denaturation |
1-3 min | 95°C |
30-40 Cycles: Denaturation Annealing Extension |
15-30 sec 30-65 sec 30 sec (per 500bp) |
95°C 55-65°C 72-75°C |
Note:
an individual optimization of annealing temperature may be necessary for new combinations of primers and Template DNA
Manufactured and quality-controlled in accordance with DIN EN ISO 9001 and DIN EN ISO14001
Hot-Start Polymerase for qPCR, dATP, dCTP, dGTP, dUTP, optimized reaction buffer with KCl, Ammonium Sulfate and MgCl2, stabilizers and enhancers,
* availibility of sample size may be limited
Final price excl. shipping costs3
qPCR MultiplexMastermix
Hot-Start Polymerase for qPCR, dATP, dCTP, dGTP, dUTP, LOW ROX, optimized reaction buffer with KCl, Ammonium Sulfate and MgCl2, stabilizers and enhancers,
* availibility of sample size may be limited
Final price excl. shipping costs3
Hot-Start Polymerase for qPCR, dATP, dCTP, dGTP, dUTP, HIGH ROX, optimized reaction buffer with KCl, Ammonium Sulfate and MgCl2, stabilizers and enhancers,
* availibility of sample size may be limited
Final price excl. shipping costs3