Literature DB >> 30710024

Nested Polymerase Chain Reaction (PCR).

Michael R Green, Joseph Sambrook.   

Abstract

Nested polymerase chain reaction (PCR) is used in situations in which it is necessary to increase the sensitivity and/or specificity of PCR, for example, when amplifying a particular member of a polymorphic gene family or when amplifying a cDNA copy of an mRNA present at very low abundance in a clinical specimen containing a heterogeneous population of cell types. Nested PCR usually involves two sequential amplification reactions, each of which uses a different pair of primers. The product of the first amplification reaction is used as the template for the second PCR, which is primed by oligonucleotides that are placed internal to the first primer pair. The use of two pairs of oligonucleotides allows a higher number of cycles to be performed, thereby increasing the sensitivity of the PCR. The improved specificity of the reaction derives from the binding of two separate sets of primers to the same target template. Nested PCR is an efficient method to amplify segments of long templates but requires knowledge of the sequence of the target.
© 2019 Cold Spring Harbor Laboratory Press.

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Year:  2019        PMID: 30710024     DOI: 10.1101/pdb.prot095182

Source DB:  PubMed          Journal:  Cold Spring Harb Protoc        ISSN: 1559-6095


  8 in total

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Review 2.  Application Progress of High-Throughput Sequencing in Ocular Diseases.

Authors:  Xuejun He; Ningzhi Zhang; Wenye Cao; Yiqiao Xing; Ning Yang
Journal:  J Clin Med       Date:  2022-06-17       Impact factor: 4.964

3.  Meta-analysis of variable-temperature PCR technique performance for diagnosising Schistosoma japonicum infections in humans in endemic areas.

Authors:  Meng-Tao Sun; Man-Man Gu; Jie-Ying Zhang; Qiu-Fu Yu; Poppy H L Lamberton; Da-Bing Lu
Journal:  PLoS Negl Trop Dis       Date:  2022-01-14

4.  Molecular Characterization of Microbiota in Cerebrospinal Fluid From Patients With CSF Shunt Infections Using Whole Genome Amplification Followed by Shotgun Sequencing.

Authors:  Paul Hodor; Christopher E Pope; Kathryn B Whitlock; Lucas R Hoffman; David L Limbrick; Patrick J McDonald; Jason S Hauptman; Jeffrey G Ojemann; Tamara D Simon
Journal:  Front Cell Infect Microbiol       Date:  2021-08-20       Impact factor: 5.293

5.  Rapid characterization of feline leukemia virus infective stages by a novel nested recombinase polymerase amplification (RPA) and reverse transcriptase-RPA.

Authors:  Sitthichok Lacharoje; Somporn Techangamsuwan; Nuntaree Chaichanawongsaroj
Journal:  Sci Rep       Date:  2021-11-11       Impact factor: 4.379

6.  CYP2B6 allelic variants and non-genetic factors influence CYP2B6 enzyme function.

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Journal:  Sci Rep       Date:  2022-02-22       Impact factor: 4.379

7.  Development of loop-mediated isothermal amplification-lateral flow dipstick as a rapid screening test for detecting Listeria monocytogenes in frozen food products using a specific region on the ferrous iron transport protein B gene.

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Journal:  Vet World       Date:  2022-03-12

Review 8.  New Perspectives for Whole Genome Amplification in Forensic STR Analysis.

Authors:  Richard Jäger
Journal:  Int J Mol Sci       Date:  2022-06-25       Impact factor: 6.208

  8 in total

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