Detection of the R553X DNA single point mutation related to cystic fibrosis by a "chiral box" D-lysine-peptide nucleic acid probe by capillary electrophoresis

Electrophoresis

Volumn 26, Issue 22, 2005, Pages 4310-4316

  Tedeschi, Tullia ^a   Chiari, Marcella ^b   Galaverna, Gianni ^a   Sforza, Stefano ^a   Cretich, Marina ^b   Corradini, Roberto ^a   Marchelli, Rosangela ^a  

^a UNIVERSITY OF PARMA   (Italy)

^b CNR   (Italy)

Author keywords

Capillary electrophoresis; Cystic fibrosis; DNA; Peptide nucleic acids; Single nucleotide polymorphism

Indexed keywords

AMINO ACIDS; CAPILLARY ELECTROPHORESIS; GENES; IONIC STRENGTH; OLIGONUCLEOTIDES; PEPTIDES; POLYMERASE CHAIN REACTION; PROBES; ULTRAVIOLET SPECTROSCOPY;

BINDING SPECIFICITIES; CYSTIC FIBROSIS; D-LYSINE; HUMAN GENOMES; MUTATED GENES; PEPTIDE NUCLEIC ACID; SINGLE NUCLEOTIDE POLYMORPHISMS; SINGLE-POINT MUTATION; SYNTHESISED;

DNA;

DEXTRO LYSINE; PEPTIDE NUCLEIC ACID; SINGLE STRANDED DNA;

ARTICLE; CAPILLARY ELECTROPHORESIS; CHIRALITY; CONTROLLED STUDY; CYSTIC FIBROSIS; ELECTROSPRAY MASS SPECTROMETRY; GENE IDENTIFICATION; HOMOZYGOSITY; HUMAN; HUMAN GENOME; NUCLEIC ACID SYNTHESIS; NUCLEOTIDE SEQUENCE; POINT MUTATION; POLYMERASE CHAIN REACTION; SEPARATION TECHNIQUE; SEQUENCE HOMOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; ULTRAVIOLET SPECTROSCOPY;

EID: 28244463898     PISSN: 01730835     EISSN: None     Source Type: Journal    
DOI: 10.1002/elps.200410390     Document Type: Article

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