Arrays of microparticle populations, each population labeled with a single fluorescent dye, are provided for use in multiplex assays. The populations form a virtual multidimensional array wherein each microparticle is identified by fluorescence intensity in two different fluorescence detection channels. The arrays are useful in a variety of assays, including multiplex, multi-analyte assays for the simultaneous detection of two or more analytes by, for example, flow cytometry, and a labeling reagents in, for example, microscopy. The use of singly-dyed microparticles to form multidimensional arrays greatly simplifies the creation of multiplex assays.
Arrays of microparticle populations, each population labeled with a single fluorescent dye, are provided for use in multiplex assays. The populations form a virtual multidimensional array wherein each microparticle is identified by fluorescence intensity in two different fluorescence detection channels. The arrays are useful in a variety of assays, including multiplex, multi-analyte assays for the simultaneous detection of two or more analytes by, for example, flow cytometry, and a labeling reagents in, for example, microscopy. The use of singly-dyed microparticles to form multidimensional arrays greatly simplifies the creation of multiplex assays.
Peridinin-Chlorophyll Complex As Fluorescent Label
Peridinin-chlorophyll-protein complexes are provided for use as fluorescent labels and are particularly useful in diagnostic assays employing as a reagent a fluorescent compound conjugated to a member of a specific binding pair, wherein the pair consists of a biochemical ligand and a receptor and the diagnostic assay comprises a step in which the conjugate binds to its complementary binding-pair member.
Multi-Color Fluorescence Analysis With Single Wavelength Excitation
Diether J. Recktenwald - Cupertino CA Chia H. Chen - San Jose CA
Assignee:
Becton Dickinson and Company - Franklin Lakes NJ
International Classification:
G01N 2164
US Classification:
2504581
Abstract:
A method for determining one or more characteristics of particles using multiple fluorescence analysis comprises directing an incident light beam at the particles under analysis. The particles include at least three fluorescent markers each having different emission spectra. The incident light beam causes the excitation of the markers by light at a single wavelength whereby different wavelengths of fluorescence are emitted from the particles. Different fluorescence emissions associated with the particles under analysis are simultaneously detected. This method further includes associating the detected fluorescence with one or more characteristics of the particles. An apparatus is also part of the present invention for carrying out the aforementioned method.
A method for improving recovery of cells from liquid suspension by centrifugation. The method comprises coating the interior of centrifuge containers with a solution comprising an amphipathic compound prior to introduction of the cell suspension and centrifugation. The method is particularly suited for recovery or concentration of rare cells from dilute suspensions, for example when rare cells are isolated from a sample by sorting on a flow cytometer.
A method for improving recovery of cells from liquid suspension by centrifuqation. The method comprises coating the interior of centrifuge containers with a solution comprising an amphipathic compound prior to introduction of the cell suspension and centrifugation. The method is suited for recovery or concentration of rare cells from dilute suspensions, for example when rare cells are isolated from a sample by sorting on a flow cytometer.
Method And Materials For Calibrating Flow Cytometers And Other Analysis Instruments
Diether J. Recktenwald - Cupertino CA Rickie S. Kerndt - Cupertino CA Michael R. Loken - Los Altos CA Chia H. Chen - San Jose CA
Assignee:
Becton, Dickinson and Company - Franklin Lakes NJ
International Classification:
G06M 1100
US Classification:
73 1R
Abstract:
A method for calibrating an instrument for using that instrument to obtain at least one light-related signal from particles under analysis comprises directing an incident beam of light at calibration particles having one or more known characteristics related to the particles expected to be analyzed. Both a light signal and a noise signal from the calibration particles are detected. A measurement is made of the ratio of the detected light signal to the detected noise signal, and that measurement is reported. The measured ratio is then compared to a predetermined ratio which represents a threshold for minimum instrument performance. This method further includes adjusting, if the predetermined ratio has not been attained, the operation of the instrument, while the calibration particles are within the incident beam of light, until the measured ratio reaches the predetermined ratio whereby the instrument is calibrated for subsequently obtaining the light signal from particles to be analyzed. A kit of reagents for use in calibrating an instrument for performing two-color analysis of particles and particle standards for calibrating fluorescence analysis instruments are also part of the instant invention.
Method For Analysis Of Subpopulations Of Blood Cells
A method for identifying and enumerating cells of a subclass of blood cells in relation to cells of another subclass of blood cells is provided. In the method a first subclass of blood cells is selectively tagged by incubating an aliquot of a blood sample with a first tagging agent. A second subclass of blood cells is selectively tagged by incubating the aliquot with a second tagging agent. The aliquot is then passed, without lysing of any subclasses of blood cells which are not of interest, substantially a cell at a time through an area of optical stimulation for the tagging agents. Light emitted by the tagging agents is detected, the detection being limited by gating to a threshold value related to a predetermined intensity of light by one of the tagging agents. Cells of the subclass are differentiated based on occurrence of emitted light from the tagging agents.
Desatoya
Principal
Bd Feb 2004 - Oct 2012
Vice President Advanced Technology
Bd Feb 2004 - Oct 2012
Bd Fellow Emeritus; Vice President Advanced Technology, Retired
Amcell Corp 1994 - 1999
Vice President R and D
Becton Dickinson Immunocytometry Systems Feb 1981 - Apr 1994
Scientist To Associate Scientific Director
Education:
Stanford University 1980 - 1981
Skills:
Flow Cytometry Assay Development Biotechnology R&D Cell Technology Transfer Lifesciences Life Sciences Medical Devices Immunology Commercialization Product Development Hardware Diagnostics Fda Biochemistry Cell Culture Infectious Diseases Biopharmaceuticals Immunoassays Oncology Molecular Biology Science Cancer Cell Biology Genomics Proteomics Program Management Fluorescence Drug Discovery Design Control Protein Chemistry Fluorescence Microscopy Product Launch Clinical Development Laboratory Automation Elisa Microscopy Data Analysis Biomedical Engineering Stem Cells Research Software Development Nanotechnology Purification Bioinformatics Technology Evaluation Personalized Medicine Diagnostics Cell Based Assays Project Planning