Developing a real-time quantitative loop-mediated isothermal amplification assay as a rapid and accurate method for detection of Brucellosis

Journal of Applied Microbiology

Volumn 115, Issue 3, 2013, Pages 828-834

  Soleimani, M ^a   Shams, S ^b   Majidzadeh A, K ^a,c  

^a AJA UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b QOM UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c AVICENNA RESEARCH INSTITUTE   (Iran)

Author keywords

Brucella; LAMP; omp25; Sensitivity; Specificity

Indexed keywords

DIAGNOSIS; ELECTROPHORESIS;

BRUCELLA; CAUSATIVE AGENTS; LOOP MEDIATED ISOTHERMAL AMPLIFICATIONS; LOOP-MEDIATED ISOTHERMAL AMPLIFICATIONS; OMP25; QUANTITATIVE TESTS; RAPID DETECTION; REAL- TIME; SENSITIVITY; SPECIFICITY;

GENES;

GENOMIC DNA;

AMPLIFICATION; BIOASSAY; BRUCELLOSIS; DNA; ELECTROKINESIS; GENE; PLASMID;

AGAR GEL ELECTROPHORESIS; ARTICLE; BRUCELLA; BRUCELLOSIS; DIAGNOSTIC ACCURACY; LOOP MEDIATED ISOTHERMAL AMPLIFICATION; NONHUMAN; NUCLEOTIDE SEQUENCE; PLASMID; SENSITIVITY AND SPECIFICITY; TURBIDIMETRY;

BRUCELLA; NEGIBACTERIA; POSIBACTERIA;

BRUCELLA; LAMP; OMP25; SENSITIVITY; SPECIFICITY;

BRUCELLA; BRUCELLOSIS; DNA PRIMERS; ELECTROPHORESIS, AGAR GEL; HUMANS; NUCLEIC ACID AMPLIFICATION TECHNIQUES; SENSITIVITY AND SPECIFICITY;

EID: 84881662744     PISSN: 13645072     EISSN: 13652672     Source Type: Journal    
DOI: 10.1111/jam.12290     Document Type: Article

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