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1.
Ann Biol Clin (Paris) ; 71(6): 717-30, 2013.
Article in French | MEDLINE | ID: mdl-24342794

ABSTRACT

Preliminary evaluation of quantitative clinical laboratory measurements is a prerequisite for the accreditation of clinical laboratories, according to the French Committee of Accreditation guidelines following the European reference Standard EN ISO 15189. Numerous papers have been published regarding biochemistry and immunology. However, data are lacking for automated complete blood count accreditation. We report here our experience at Hôpital européen Georges Pompidou hematology laboratory and present the performance characteristics of two mirrored LH750 Beckman-Coulter analysers, including precision, accuracy and uncertainty of measurement.


Subject(s)
Accreditation/methods , Automation, Laboratory , Hematologic Tests/instrumentation , Hematologic Tests/standards , Automation, Laboratory/instrumentation , Automation, Laboratory/standards , Blood Cell Count/instrumentation , Blood Cell Count/standards , Equipment Contamination , France , Hospitals, Public/standards , Humans , Paris , Quality Control , Reproducibility of Results , Risk Management , Sensitivity and Specificity , Uncertainty
2.
FEMS Microbiol Lett ; 313(1): 81-7, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20946385

ABSTRACT

The aim of this study was to develop a system for rapid and accurate real-time quantitative PCR (qPCR) identification and quantification of Botrytis cinerea, one of the major pathogens present on grapes. The intergenic spacer (IGS) region of the nuclear ribosomal DNA was used to specifically detect and quantify B. cinerea. A standard curve was established to quantify this fungus. The qPCR reaction was based on the simultaneous detection of a specific IGS sequence and also contained an internal amplification control to compensate for variations in DNA extraction and the various compounds from grapes that inhibit PCR. In these conditions, the assay had high efficiency (97%), and the limit of detection was estimated to be 6.3 pg DNA (corresponding to 540 spores). Our method was applied to assess the effects of various treatment strategies against Botrytis in the vineyard. Our qPCR assay proved to be rapid, selective and sensitive and may be used to monitor Botrytis infection in vineyards.


Subject(s)
Botrytis/physiology , Polymerase Chain Reaction , Vitis/microbiology , Benzothiazoles , Botrytis/genetics , Botrytis/isolation & purification , Calibration , DNA, Fungal/analysis , Diamines , Food Handling/standards , Organic Chemicals/chemistry , Quinolines , Sensitivity and Specificity
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