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PCR

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Cover of 'PCR'

Table of Contents

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    Book Overview
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    Chapter 1 In Silico PCR Tools for a Fast Primer, Probe, and Advanced Searching
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    Chapter 2 Introduction on Using the FastPCR Software and the Related Java Web Tools for PCR and Oligonucleotide Assembly and Analysis.
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    Chapter 3 Long Fragment Polymerase Chain Reaction.
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    Chapter 4 Strategies to Improve Efficiency and Specificity of Degenerate Primers in PCR
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    Chapter 5 Inverse PCR for Point Mutation Introduction
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    Chapter 6 Synthesis of Fusion Genes for Cloning by Megaprimer-Based PCR
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    Chapter 7 A Novel Platform for High-Throughput Gene Synthesis to Maximize Recombinant Expression in Escherichia coli.
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    Chapter 8 Colony PCR
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    Chapter 9 CRENAME, A Molecular Microbiology Method Enabling Multiparametric Assessment of Potable/Drinking Water
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    Chapter 10 Multiplex Detection of Food-Borne Pathogens
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    Chapter 11 Fast Real-Time PCR for the Detection of Crustacean Allergens in Foods
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    Chapter 12 Fast Real-Time PCR Method for Detection of Soy in Foods
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    Chapter 13 RAPD/SCAR Approaches for Identification of Adulterant Breeds’ Milk in Dairy Products
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    Chapter 14 Genetic Diversity Analysis of Medicinally Important Horticultural Crop Aegle marmelos by ISSR Markers
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    Chapter 15 PCR in the Analysis of Clinical Samples: Prenatal and Postnatal Diagnosis of Inborn Errors of Metabolism
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    Chapter 16 Harnessing the Power of PCR Molecular Fingerprinting Methods and Next Generation Sequencing for Understanding Structure and Function in Microbial C... - PubMed - NCBI
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    Chapter 17 PCR in Metagenomics
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    Chapter 18 Arbitrarily Primed PCR for Comparison of Meta Genomes and Extracting Useful Loci from Them
Attention for Chapter 3: Long Fragment Polymerase Chain Reaction.
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Chapter title
Long Fragment Polymerase Chain Reaction.
Chapter number 3
Book title
PCR
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7060-5_3
Pubmed ID
Book ISBNs
978-1-4939-7059-9, 978-1-4939-7060-5
Authors

Eng Wee Chua, Simran Maggo, Martin A. Kennedy

Editors

Lucília Domingues

Abstract

Polymerase chain reaction (PCR) is an oft-used preparatory technique in amplifying specific DNA regions for downstream analysis. The size of an amplicon was initially limited by errors in nucleotide polymerization and template deterioration during thermal cycling. A variant of PCR, designated long-range PCR, was devised to counter these drawbacks and enable the amplification of large fragments exceeding a few kb. In this chapter we describe a protocol for long-range PCR, which we have adopted to obtain products of 6.6, 7.2, 13, and 20 kb from human genomic DNA samples.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 31 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 31 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 16%
Other 3 10%
Student > Bachelor 3 10%
Student > Postgraduate 3 10%
Student > Ph. D. Student 3 10%
Other 5 16%
Unknown 9 29%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 9 29%
Agricultural and Biological Sciences 7 23%
Pharmacology, Toxicology and Pharmaceutical Science 2 6%
Unspecified 1 3%
Computer Science 1 3%
Other 3 10%
Unknown 8 26%