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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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Analysis Note: Protein determined by Biuret. Physical form: Suspension in 3.2 M (NH 4 ) 2 SO 4 , pH 7.0 Preparation Note: Affinity purified • Physical Form: ammonium sulfate suspension • Ad
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Selective media for Salmonella
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