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Distinction of Paramecium strains by a combination method of RAPD analysis and multiplex PCR
by
Watanabe, Kenta
, Shimizu, Takashi
, Tachibana, Masato
, Watarai, Masahisa
, Kiyota, Hiroko
, Matsumoto, Sonoko
in
Aging
/ Amplification
/ Analysis
/ Annealing
/ Bacteria
/ Biology and Life Sciences
/ Classification
/ Cloning
/ Comparative analysis
/ Conjugation
/ Deoxyribonucleic acid
/ DNA
/ Environmental management
/ Genes
/ Genetic aspects
/ Genetic polymorphisms
/ Genetic testing
/ Genomes
/ Identification and classification
/ Laboratories
/ Morphology
/ Motility
/ Multiplex Polymerase Chain Reaction
/ Multiplexing
/ Paramecia
/ Paramecium
/ Paramecium - genetics
/ Physical characteristics
/ Polymerase chain reaction
/ Polymorphism
/ Public health
/ Random amplified polymorphic DNA
/ Random Amplified Polymorphic DNA Technique - methods
/ Reproducibility
/ Research and Analysis Methods
/ Strains (organisms)
/ Symbiosis
/ Veterinary colleges
/ Veterinary medicine
2022
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Distinction of Paramecium strains by a combination method of RAPD analysis and multiplex PCR
by
Watanabe, Kenta
, Shimizu, Takashi
, Tachibana, Masato
, Watarai, Masahisa
, Kiyota, Hiroko
, Matsumoto, Sonoko
in
Aging
/ Amplification
/ Analysis
/ Annealing
/ Bacteria
/ Biology and Life Sciences
/ Classification
/ Cloning
/ Comparative analysis
/ Conjugation
/ Deoxyribonucleic acid
/ DNA
/ Environmental management
/ Genes
/ Genetic aspects
/ Genetic polymorphisms
/ Genetic testing
/ Genomes
/ Identification and classification
/ Laboratories
/ Morphology
/ Motility
/ Multiplex Polymerase Chain Reaction
/ Multiplexing
/ Paramecia
/ Paramecium
/ Paramecium - genetics
/ Physical characteristics
/ Polymerase chain reaction
/ Polymorphism
/ Public health
/ Random amplified polymorphic DNA
/ Random Amplified Polymorphic DNA Technique - methods
/ Reproducibility
/ Research and Analysis Methods
/ Strains (organisms)
/ Symbiosis
/ Veterinary colleges
/ Veterinary medicine
2022
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Distinction of Paramecium strains by a combination method of RAPD analysis and multiplex PCR
by
Watanabe, Kenta
, Shimizu, Takashi
, Tachibana, Masato
, Watarai, Masahisa
, Kiyota, Hiroko
, Matsumoto, Sonoko
in
Aging
/ Amplification
/ Analysis
/ Annealing
/ Bacteria
/ Biology and Life Sciences
/ Classification
/ Cloning
/ Comparative analysis
/ Conjugation
/ Deoxyribonucleic acid
/ DNA
/ Environmental management
/ Genes
/ Genetic aspects
/ Genetic polymorphisms
/ Genetic testing
/ Genomes
/ Identification and classification
/ Laboratories
/ Morphology
/ Motility
/ Multiplex Polymerase Chain Reaction
/ Multiplexing
/ Paramecia
/ Paramecium
/ Paramecium - genetics
/ Physical characteristics
/ Polymerase chain reaction
/ Polymorphism
/ Public health
/ Random amplified polymorphic DNA
/ Random Amplified Polymorphic DNA Technique - methods
/ Reproducibility
/ Research and Analysis Methods
/ Strains (organisms)
/ Symbiosis
/ Veterinary colleges
/ Veterinary medicine
2022
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Distinction of Paramecium strains by a combination method of RAPD analysis and multiplex PCR
Journal Article
Distinction of Paramecium strains by a combination method of RAPD analysis and multiplex PCR
2022
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Overview
Paramecium is employed as a valuable model organism in various research fields since a large number of strains with different characteristics of size, morphology, degree of aging, and type of conjugation can be obtained. It is necessary to determine a method for the classification and simple identification of strains to increase their utility as a research tool. This study attempted to establish a polymerase chain reaction (PCR)-based method to differentiate strains of the same species. Genomic DNA was purified from several strains of P . caudatum , P . tetraurelia , and P . bursaria used for comparison by the random amplified polymorphic DNA (RAPD)-PCR method. In P . tetraurelia and P . bursaria , it was sufficiently possible to distinguish specific strains depending on the pattern of random primers and amplification characteristics. For the classification of P . caudatum , based on the sequence data obtained by RAPD-PCR analysis, 5 specific primer sets were designed and a multiplex PCR method was developed. The comparative analysis of 2 standard strains, 12 recommended strains, and 12 other strains of P . caudatum provided by the National BioResource Project was conducted, and specific strains were identified. This multiplex PCR method would be an effective tool for the simple identification of environmental isolates or the management of Paramecium strains.
Publisher
Public Library of Science,Public Library of Science (PLoS)
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