ranscription efficiency.
C.
therm Polymerase for Reverse Transcription in Two-Step RT-PCR
C. therm. Polymerase easily overcomes structure and sensitivity problems
encountered during RT-PCR reactions. This magnesium-dependent polymerase
exhibits optimal activity between 60C and 70C (maximum of 72C), dramatically
reducing RNA secondary structure and increasing transcription efficiency.
Expand
High Fidelity PCR System
Expand High Fidelity PCR System delivers superior PCR results with a greater
than two-fold higher yield and three-fold greater fidelity than Taq DNA
polymerase. More sensitive than Taq DNA polymerase, Expand High Fidelity
improves PCR results for genomic targets up to 5 kb in length.
Expand
High Fidelity PLUS PCR System
Roche Applied Science, which pioneered the blending of thermostable DNA
Polymerases with the Expand High Fidelity and Expand Long Template PCR
Systems, now introduces the Expand High Fidelity PLUS PCR System - the
first product of a family of next generation PCR Blends. This new blend
combines Taq DNA Polymerase with a novel proofreading protein, isolated
and characterized by Roche Applied Science. This protein mediates proofreading
activity but has no polymerase activity itself. The synergy between the
mechanism of the proofreading protein and the processivity of Taq DNA
Polymerase is the key to Expa
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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