A rapid microplate fluorescence method to detect yessotoxins based on their capacity to activate phosphodiesterases

Analytical Biochemistry

Volumn 326, Issue 1, 2004, Pages 93-99

  Alfonso, Amparo ^a   Vieytes, Mercedes R ^a   Yasumoto, Takeshi ^b   Botana, Luis M ^a  

^a UNIVERSITY OF SANTIAGO DE COMPOSTELA   (Spain)

^b JAPAN FOOD RESEARCH LABORATORIES   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ESTERS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS;

ALCOHOLIC EXTRACT; DETECTION LIMITS; FLUORESCENCE METHOD; HYDROLYSIS RATE; MONOPHOSPHATES; MOUSE BIOASSAY; PHOSPHODIESTERASES; RATE OF HYDROLYSIS;

FLUORESCENCE;

ALCOHOL; ANTHRANILIC ACID; CYCLIC AMP; ESTERASE; FLUORESCENT DYE; PHOSPHODIESTERASE; PHOSPHORUS DERIVATIVE; TOXIN; UNCLASSIFIED DRUG; YESSOTOXIN;

ACCURACY; ARTICLE; CELL LEVEL; CELLULAR DISTRIBUTION; CONCENTRATION RESPONSE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ASSAY; FLUORESCENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; INTERMETHOD COMPARISON; LINEAR REGRESSION ANALYSIS; MOLECULAR DYNAMICS; NONHUMAN; PRIORITY JOURNAL; SHELLFISH; TECHNIQUE; TOXICITY;

EID: 0842303044     PISSN: 00032697     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ab.2003.11.022     Document Type: Article

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