GeneOn :: Real-time qPCR Master mixes :: Colorless Line for qPCR :: SuperHot qPCR Master Mix RT

SuperHot qPCR Master Mix RT

SuperHot qPCR Master Mix RT

qPCR Master Mix RT: Datasheet
qPCR Master Mix: Deutsche Beschreibung

Features:
- The Master Mix (2X) offers both: high sensitivity and specificity
- Time saving ready-to-use qPCR Mastermix
- repeatable and reliable results
- efficient PCR for a wide range of template concentrations
- activation time < 3 min

Applications:
- Realtime PCR and quantitative PCR e.g. with Sybr green, Eva green or probes
- High-throughput PCR
- Multiplex PCR
- Low copy targets PCR

Description:
The 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.

Concentration: The Mastermix is 2x concentrated

List of components qPCR / RTD-PCR Master mix.
Hot-Start Polymerase (m-Superhot-Taq) for qPCR, dATP, dCTP, dGTP, dTTP, reaction buffer with  stabilizers and enhancers, 1 Tube PCR-grade water, 1 Tube MgCl2

Quality control:
- Performance and purity tests
- Endodeoxyribonuclease Assay
- Real time PCR Test with SmartCycler II
- PCR Test with Lambda DNA (12 kb-fragment) and human placental DNA (3 kb-fragment)

Transportation: on blue ice

Storage: at 4°C for 3 months, at -20°C for more than 12 months


 Components  Volume per reaction  final conc.
 2X qPCR / RTD-PCR Master Mix RT  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
 reference dye (optional)   x µl  NA
 Template DNA  5 µl
 (0.1-15 ng/ml plasmid DNA)
 (1-10 µg/ml genomic DNA)
 < 500ng DNA
 Sterile dest. Water (included)  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
Note: Do not use DMSO or Formamide

General Thermo-Cycler protocol:

 

 Step  Time  Temperature
 Initial denaturation  1-3 min  95°C
 
35-50 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

Product code: S240  
 
Your Shop-price: 89,00
31%
Market price: € 129,00
Quantity