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The polymerase chain reaction
Authors:J Bell
Affiliation:1. Department of Chemistry, William Jewell College, 500 College Hill, Liberty, MO 64068, United States;2. Department of Chemistry, University of Iowa, E331 Chemistry Building, Iowa City, IA 52242-1294, United States;1. Gastroenterology Department, Grupo de Estudo de Nutrição Entérica (GENE), Enteral Feeding Team, Hospital Garcia de Orta, Almada, Portugal;2. Grupo de Estudo de Nutrição Entérica (GENE), Enteral Feeding Team, Hospital Garcia de Orta, Almada, Portugal;1. Department of Molecular Biology, Faculty of Natural Sciences, Comenius University, Ilkovicova 6, Bratislava, 842 15, Slovakia;2. Department of Paediatric Neurology, Faculty of Medicine, Comenius University and National Institute of Children''s Diseases, Limbova 1, 833 40, Bratislava, Slovakia;3. Institute for Clinical and Translational Research, Biomedical Research Centre, Slovak Academy of Sciences, Dubravska cesta 9, 845 05, Bratislava, Slovakia;4. Medirex a.s., MEDIREX GROUP, Holubyho 35, 902 01, Pezinok, Slovakia
Abstract:The polymerase chain reaction (PCR) is a novel technique that amplifies specific sequences with remarkable efficiency. Repeated cycles of denaturation, primer annealling and extension carried out with the heat stable enzyme, Taq polymerase, leads to exponential increases in the target DNA sequences. The technique has been widely applied in immunology to define HLA polymorphism, T-cell receptor and immunoglobulin diversity, pathogen detection, quantification of lymphokines and lymphoma or leukaemia detection. In addition, it has been very widely applied in all areas of molecular biology and human genetics. Because of its simplicity and sensitivity, PCR represents a major technical development for molecular biologists and will continue to have a great impact on molecular immunology. This review by John Bell describes the basic PCR technique and some variations on it and briefly explores their uses in molecular immunology.
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