Dean Burgi - Sunnyvale CA, US Stephen Williams - San Carlos CA, US
International Classification:
G01N027/453
US Classification:
204452000, 204603000
Abstract:
The present invention is directed to methods for identifying one or more analytes in a sample using electrophoresis. In one embodiment, the method comprises performing an electrophoretic separation by applying a potential across the separation path and thus generating a current and power therein and producing an electropherogram, integrating the current or the power to determine the cumulative current or power as a function of the separation time, transforming the electropherogram to a second electropherogram representing the signal as a function of the cumulative current or power, and identifying in the second electropherogram peaks that are correlated with the analytes in the sample. The invention also provides systems for performing the analysis and identification methods, as well as computer-readable products for performing the steps associated with the above methods.
Katariina Hutterer - Santa Barbara CA, US Nels Olson - La Jolla CA, US Stevan Jovanovich - Livermore CA, US Thomas Armstrong - Santa Clara CA, US Dean Burgi - Sunnyvale CA, US Vladislav Dolnik - Mountain View CA, US
International Classification:
G01N027/453
US Classification:
204456000, 204605000
Abstract:
Multi-capillary systems for high-throughput electrophoretic separation and detection of biomolecules are disclosed. One embodiment of the invention uses galactomannans as a size-sieving matrix for multi-channel electrophoretic separations of biomolecules. Multi-color detection for the simultaneous analysis of controls and standards in the same channels as the samples, and endogenous fluorescence detection are also disclosed. Another embodiment of the invention is a two dimensional system for separation of complex samples, using multiplexed capillary electrophoresis system as the second dimension, with a fraction collection step connecting the two separation steps. The systems allow for separations to be accomplished with a highly parallel manner, or in a two-dimensional format.
Analyte Identification In Transformed Electropherograms
Dean Burgi - South San Francisco CA, US Stephen Williams - South San Francisco CA, US
International Classification:
B01D 57/02 G01N 27/00
US Classification:
204452000, 204603000
Abstract:
The present invention is directed to methods for identifying one or more analytes in a sample using electrophoresis. In one embodiment, the method comprises performing an electrophoretic separation by applying a potential across the separation path and thus generating a current and power therein and producing an electropherogram, integrating the current or the power to determine the cumulative current or power as a function of the separation time, transforming the electropherogram to a second electropherogram representing the signal as a function of the cumulative current or power, and identifying in the second electropherogram peaks that are correlated with the analytes in the sample. The invention also provides systems for performing the analysis and identification methods, as well as computer-readable products for performing the steps associated with the above methods.
System For Analysis Of X-Ray Films Of Nucleotide Sequences
Dean S. Burgi - Menlo Park CA Daniel M. Bartell - Foster City CA Donald D. Sleeter - San Leandro CA Lucina P. Mastro - San Francisco CA
Assignee:
Genomyx Corporation - Foster City CA
International Classification:
G06K 900
US Classification:
382129
Abstract:
A system for identification of DNA bases in a nucleotide sequence includes a microprocessor and a set of executable instructions and is configured to accept a set of input data corresponding to a DNA sequence image from an autoradiograph. In part by interpolating a distribution of density peaks derived from the set of input data, the system is configured to generate a set of output data substantially identifying or presenting the bases in the DNA sequence in a linear fashion, corresponding to the linear order of nucleotides comprising the DNA sequence. The system thereby enables identification of substantially more bases than could be read by the human eye. Enhanced electrophoresis equipment and consumables may also be applied to generate a more predictable and linear set of input data and, in turn, to generate a set of output data identifying an even greater number of DNA bases in the sequence under analysis.
Field Amplified Polarity Switching Sample Injection In Capillary Zone Electrophoresis
An improved electroinjection method of introducing a sample having positive and negative ions into a capillary column for CE or CZE process by introducing a short plug of a low concentration buffer before introducing the sample into the column which results in increasing amount of charged ions of the sample introduced in the capillary column due to increasing the electric field at the injection point. A method for efficiently introducing both positive and negative ions is also shown.
System And Method For Improving Sample Concentration In Capillary Electrophoresis
The method for improving sample concentration in capillary electrophoresis by extracting the sample buffer from the capillary column using the electro-osmotic flow while the sample components are stacked into the support buffer utilizes a system for this technique. The system has a separation column 11, sample introduction means 16 for injecting the sample solution, an injection detector means 20 for detecting the volume of injected sample solution, a separation detector means 21 for detecting the sample components, power supply means 17 for applying a high voltage along the separation column 11 for reversing the direction of the electro-osmotic flow thereby causing extraction of the sample buffer from the separation column and afterward providing the separation sample into its components.
A method for drying electrophoresis gel comprising, in combination, using a gaseous moisture removing medium, a gaseous moisture removing medium driving means, and an impingement means, whereby the gaseous moisture removing medium is driven by the gaseous moisture removing medium driving means across the impingement means to provide a flow of the gaseous moisture removing medium on the surface of the gel plates, whereby the flow induced by passage of the gaseous moisture removing medium through the impingement means thereby minimizes temperature gradients within the gel by forced convection and reduces drying time of the gel.
Control Of Temperature Gradients During Gel Electrophoresis Using Turbulent Gas Flow
Douglas H. Smith - Los Altos CA Brian J. Mifsud - San Francisco CA Dean S. Burgi - Menlo Park CA Thomas E. Davis - San Francisco CA Steven M. VanHuystee - San Mateo CA
Assignee:
Genomyx Inc. - Foster City CA
International Classification:
C25B 900
US Classification:
204621
Abstract:
A gel electrophoresis separation apparatus comprising, in combination, a gaseous heat-exchange medium, a gaseous heat-exchange medium driving means, and an impingement means, whereby the gaseous heat-exchange medium is driven by the gaseous heat-exchange medium driving means across the impingement means to provide a flow of the gaseous heat-exchange medium on the surface of the gel plates, whereby the flow induced by passage of the gaseous heat-exchange medium through the impingement means thereby minimizes temperature gradients within the gel by forced convection.
Name / Title
Company / Classification
Phones & Addresses
Dean S. Burgi President, Owner
DBQP, INC
767 Mohagany Ln, Sunnyvale, CA 94086 767 Mahogany Ln, Sunnyvale, CA 94086 (408)7394199