is activated by a 4-minute heat-activation step at 95C. Minimize non-specific
amplification products and amplify even the most problematic templates (GC-rich
sequences, repeats, high secondary structure) with the optimized buffer
system and the revolutionary GC-RICH Resolution Solution.
GC-RICH PCR
System
The GC-Rich PCR System, a blend of Taq DNA polymerase and a proofreading
polymerase, powers through templates that are difficult or impossible to
amplify with other polymerases or additives. The enhanced processivity of
the blend and the unique GC-RICH Resolution Solution combine to deliver
superior performance especially from problematic templates.
High
Fidelity PCR Master
High Fidelity PCR Master contains all necessary reagents (buffers, nucleotides
and enzymes) needed for PCR. The mix contains a unique enzyme blend of Taq
DNA Polymerase and Pwo DNA Polymerase[a thermostable enzyme with a proofreading
(3'5' exonuclease) activity]. High Fidelity PCR Master amplifies with threefold
greater accuracy than Taq DNA Polymerase alone and gives better results
with impure templates because it is less affected by contaminants in a
DNA preparation than other DNA polymerases.
PCR
Core KitPLUS
The PCR Core KitPLUS is a convenient kit with ready-to-use reagents which
has been specially designed for performing PCR with Taq polymerase and carry-over
prevention.
'"/>Source:
Page: All 1 2 3 4 5 6 7 Related biology technology :1.
A New C-Terminal GST Vector for Protein Production in S. pombe2.
Safe Production of High-Titer Retrovirus3.
Production of Full-Length, Biologically Active MEK1WT and MEK1CA4.
Yeast Protein Production System Features High Yields and One-Step
Purification5.
Identification of Differentially Expressed Gene Products with the CastAway
System*6.
High-Throughput System Generates Ultra-Pure PCR Products Suitable for All
Applications7.
Identification of Low-Level Oxidation Products in Calmodulin Using NanoSpray
Ion Trap Mass Spectrometry8.
Isolation of Low Molecular Weight Digestion Products of the Human Platelet Thromboxane A2 Receptor, Rev A9.
Separation of 16S rRNA PCR Products From a Model Community Using Temporal Temperature Gradient Gel Electrophoresis, Rev A10.
Comparison of PCR Kleen Spin Columns to Traditional Methods for Purification of PCR Products Prior to Sequencing, Rev A11.
Identification of Nonspecific Products Using Melt-Curve Analysis on the iCycler iQ Detection System, Rev A