Rapid DNA typing of HLA-B27 allele by real-time PCR using lightcycler technology

Clinical Laboratory

Volumn 47, Issue 3-4, 2001, Pages 131-134

  Tiemann, C ^a   Vogel, A ^a   Dufaux, B ^a   Zimmer, M ^a   Krone, J R ^a   Hagedorn, H J ^a  

^a Medizinal Untersuchungsstelle ^*  (Germany)

Author keywords

HLA B27; LightCycler ; Polymerase chain reaction; SYBR Green I

Indexed keywords

BETA GLOBIN; DNA; DYE; HLA B27 ANTIGEN;

ALLELE; ARTICLE; CONTROLLED STUDY; COST EFFECTIVENESS ANALYSIS; DIAGNOSTIC PROCEDURE; DNA DENATURATION; EXON; GENE AMPLIFICATION; GENE TECHNOLOGY; HLA TYPING; HUMAN; LABORATORY TEST; MELTING POINT; POLYMERASE CHAIN REACTION; RELIABILITY; SENSITIVITY AND SPECIFICITY;

ALLELES; BIOMEDICAL TECHNOLOGY; DNA; FLUORESCENCE; HISTOCOMPATIBILITY TESTING; HLA-B27 ANTIGEN; HUMANS; POLYMERASE CHAIN REACTION; TIME FACTORS;

EID: 0035086534     PISSN: 14336510     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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16. Rapid differentiation of Borrelia garinii from Borrelia afzelii and Borrelia burgdorferi sensu stricto by LightCycler fluorescence melting curve analysis of a PCR product of the recA gene