Two-stage isothermal enzymatic amplification for concurrent multiplex molecular detection

Clinical Chemistry

Volumn 63, Issue 3, 2017, Pages 714-722

  Song, Jinzhao ^a   Liu, Changchun ^a   Mauk, Michael G ^a   Rankin, Shelley C ^b   Lok, James B ^b   Greenberg, Robert M ^b   Bau, Haim H ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; FLUORESCENT DYE; RNA;

AMPLICON; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BLOOD SAMPLING; BRUGIA MALAYI; CONTROLLED STUDY; DUBBED RAPID AMPLIFICATION; ENZYMATIC ASSAY; FLUORESCENCE; GENOTYPE; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 SUBTYPE B; HUMAN PAPILLOMAVIRUS TYPE 16; HUMAN PAPILLOMAVIRUS TYPE 18; HUMAN PAPILLOMAVIRUS TYPE 35; HUMAN PAPILLOMAVIRUS TYPE 45; HUMAN PAPILLOMAVIRUS TYPE 52; HYBRIDIZATION; ISOTHERMAL AMPLIFICATION ASSAY; LIMIT OF DETECTION; LOOP MEDIATED ISOTHERMAL AMPLIFICATION; MOUSE; MULTIPLEX POLYMERASE CHAIN REACTION; NONHUMAN; PLASMODIUM FALCIPARUM; POINT OF CARE TESTING; REACTION TIME; REACTOR; SALMONELLA; SCHISTOSOMA HAEMATOBIUM; SCHISTOSOMA JAPONICUM; SCHISTOSOMA MANSONI; SCHISTOSOMIASIS MANSONI; SENSITIVITY AND SPECIFICITY; SMARTPHONE; STRONGYLOIDES STERCORALIS; WART VIRUS; ZIKA VIRUS; MICROFLUIDIC ANALYSIS; NUCLEIC ACID AMPLIFICATION; POINT OF CARE SYSTEM; TEMPERATURE;

HUMANS; MICROFLUIDIC ANALYTICAL TECHNIQUES; MULTIPLEX POLYMERASE CHAIN REACTION; NUCLEIC ACID AMPLIFICATION TECHNIQUES; POINT-OF-CARE SYSTEMS; TEMPERATURE;

EID: 85014439840     PISSN: 00099147     EISSN: 15308561     Source Type: Journal    
DOI: 10.1373/clinchem.2016.263665     Document Type: Article

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