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Amplification of β-globin, K-ras 12, p53 (exon 5, exon 6) Genes from 10-Year-Old Paraffin Sections

5 Oct 2014

Application Notes

Comparison of the Sensitivity of TaKaRa Taq™ and TaKaRa Ex Taq® for Detection of <i>Helicobacter pylori</i> in Patient Samples

1 Oct 2014

Application Notes

Comparison of PCR Kleen™Spin Columns to Traditional Methods for Purification of PCR Products Prior to Sequencing

29 Sept 2014

Application Notes

Fast PCR using PrimeSTAR® Max DNA Polymerase vs. Other High-Fidelity Polymerases

25 Sept 2014

Application Notes

Quick DNA Extraction from Rice Seed (Wet)

23 Sept 2014

Application Notes

Automating the Promega GoTaq® PCR Core System II Reaction Using the Gilson PIPETMAX® 268

22 Sept 2014

Application Notes

High-Throughput Cloning of Functional Elements in the Human Genome

21 Sept 2014

Application Notes

Selecting the Proper Pipetting Tools for Optimal PCR and qPCR in the Laboratory

21 Sept 2014

Application Notes

Direct PCR from Plant Material is a Challenging Application as a Result of the Diversity of Plant Tissue Types and the Potent PCR Inhibitors Contained within the Tissue

19 Sept 2014

Application Notes

KAPA2G™ Fast HotStart Multiplex PCR

18 Sept 2014

Application Notes

Amplification of Long Products from Human Genomic DNA

18 Sept 2014

Application Notes

Fast qPCR with Takara SYBR® Premix Ex Taq

18 Sept 2014

Application Notes

KAPA2GTM Robust HotStart Mouse Genotyping

11 Sept 2014

Scientific Posters

Considerations for Use of Taq Polymerase in Molecular Diagnostic Assays

9 Sept 2014

Scientific Posters

Development of the PowerPlex® Fusion System

9 Sept 2014

Application Notes

Straightforward PCR Optimization and Highly Flexible Operation on the Dual Block Thermocycler Mastercycler Nexus GX2

26 Aug 2014

Application Notes

KAPA™ SYBR® FAST qPCR Kits Mouse Genotyping

21 Aug 2014

Application Notes

Gene Expression II Relative Quantification

16 Aug 2014

Case Studies

Workflow Improvement for PCR-based Genetic Testing: Protocol Consolidation, Decreased Cycle Times, and Increased Pass Rates

14 Aug 2014

Application Notes

Gene Expression I Housekeeping Genes

14 Aug 2014

Application Notes

Routine High-Fidelity Amplification of Longer DNA Fragments is Challenging Due to the Low Processivity and Lack of Robustness of Most Proofreading DNA Polymerases

13 Aug 2014

Application Notes

Dye- and Probe-based qPCR Using the 0.5 to 20 µL Liquidator™ 96

12 Aug 2014

Application Notes

Site-Directed Mutagenesis

12 Aug 2014

Application Notes

Current Workflows for the Extraction and Amplification of DNA for Mouse Genotyping can Benefit from Improvements in Throughput, Turnaround Time and Reliability

11 Aug 2014

Scientific Posters

Cancer Resequencing on Roche GS FLX Using KAPAHiFi™ DNA Polymerase

7 Aug 2014

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Selected Filters:

Amplification of β-globin, K-ras 12, p53 (exon 5, exon 6) Genes from 10-Year-Old Paraffin Sections

Comparison of the Sensitivity of TaKaRa Taq™ and TaKaRa Ex Taq® for Detection of <i>Helicobacter pylori</i> in Patient Samples

Comparison of PCR Kleen™Spin Columns to Traditional Methods for Purification of PCR Products Prior to Sequencing

Fast PCR using PrimeSTAR® Max DNA Polymerase vs. Other High-Fidelity Polymerases

Quick DNA Extraction from Rice Seed (Wet)

Automating the Promega GoTaq® PCR Core System II Reaction Using the Gilson PIPETMAX® 268

High-Throughput Cloning of Functional Elements in the Human Genome

Selecting the Proper Pipetting Tools for Optimal PCR and qPCR in the Laboratory

Direct PCR from Plant Material is a Challenging Application as a Result of the Diversity of Plant Tissue Types and the Potent PCR Inhibitors Contained within the Tissue

KAPA2G™ Fast HotStart Multiplex PCR

Amplification of Long Products from Human Genomic DNA

Fast qPCR with Takara SYBR® Premix Ex Taq

KAPA2GTM Robust HotStart Mouse Genotyping

Considerations for Use of Taq Polymerase in Molecular Diagnostic Assays

Development of the PowerPlex® Fusion System

Straightforward PCR Optimization and Highly Flexible Operation on the Dual Block Thermocycler Mastercycler Nexus GX2

KAPA™ SYBR® FAST qPCR Kits Mouse Genotyping

Gene Expression II Relative Quantification

Workflow Improvement for PCR-based Genetic Testing: Protocol Consolidation, Decreased Cycle Times, and Increased Pass Rates

Gene Expression I Housekeeping Genes

Routine High-Fidelity Amplification of Longer DNA Fragments is Challenging Due to the Low Processivity and Lack of Robustness of Most Proofreading DNA Polymerases

Dye- and Probe-based qPCR Using the 0.5 to 20 µL Liquidator™ 96

Site-Directed Mutagenesis

Current Workflows for the Extraction and Amplification of DNA for Mouse Genotyping can Benefit from Improvements in Throughput, Turnaround Time and Reliability

Cancer Resequencing on Roche GS FLX Using KAPAHiFi™ DNA Polymerase

Resources

Resources FilterResources Filter

Search

Selected Filters:

Amplification of β-globin, K-ras 12, p53 (exon 5, exon 6) Genes from 10-Year-Old Paraffin Sections

Comparison of the Sensitivity of TaKaRa Taq™ and TaKaRa Ex Taq® for Detection of <i>Helicobacter pylori</i> in Patient Samples

Comparison of PCR Kleen™Spin Columns to Traditional Methods for Purification of PCR Products Prior to Sequencing

Fast PCR using PrimeSTAR® Max DNA Polymerase vs. Other High-Fidelity Polymerases

Quick DNA Extraction from Rice Seed (Wet)

Automating the Promega GoTaq® PCR Core System II Reaction Using the Gilson PIPETMAX® 268

High-Throughput Cloning of Functional Elements in the Human Genome

Selecting the Proper Pipetting Tools for Optimal PCR and qPCR in the Laboratory

Direct PCR from Plant Material is a Challenging Application as a Result of the Diversity of Plant Tissue Types and the Potent PCR Inhibitors Contained within the Tissue

KAPA2G™ Fast HotStart Multiplex PCR

Amplification of Long Products from Human Genomic DNA

Fast qPCR with Takara SYBR® Premix Ex Taq

KAPA2GTM Robust HotStart Mouse Genotyping

Considerations for Use of Taq Polymerase in Molecular Diagnostic Assays

Development of the PowerPlex® Fusion System

Straightforward PCR Optimization and Highly Flexible Operation on the Dual Block Thermocycler Mastercycler Nexus GX2

KAPA™ SYBR® FAST qPCR Kits Mouse Genotyping

Gene Expression II Relative Quantification

Workflow Improvement for PCR-based Genetic Testing: Protocol Consolidation, Decreased Cycle Times, and Increased Pass Rates

Gene Expression I Housekeeping Genes

Routine High-Fidelity Amplification of Longer DNA Fragments is Challenging Due to the Low Processivity and Lack of Robustness of Most Proofreading DNA Polymerases

Dye- and Probe-based qPCR Using the 0.5 to 20 µL Liquidator™ 96

Site-Directed Mutagenesis

Current Workflows for the Extraction and Amplification of DNA for Mouse Genotyping can Benefit from Improvements in Throughput, Turnaround Time and Reliability

Cancer Resequencing on Roche GS FLX Using KAPAHiFi™ DNA Polymerase

Resources Filter