Randy M. McCormick - Santa Clara CA Gary J. Ciambrone - Redwood City CA Ian Gibbons - Portola Valley CA
Assignee:
Aclara BioSciences, Inc. - Mountain View CA
International Classification:
C02F 140
US Classification:
204601
Abstract:
Cell based assays are performed in a microfluidic device, where the cells are introduced into a reservoir and are contacted with one or more agents prior to or during their residence in the reservoir or in a capillary channel connected to the reservoir. The cells are moved by electrokinesis individually from the reservoir to a detector, where the status of the cells as a result of contacting said agents is determined. Conditions are provided for moving the cells electrophoretically or by electroosmotic force, where the cells may be viable or fixed, natural or genetically modified.
Unbiased Sample Injection For Microfluidic Applications
Qifeng Xue - Fremont CA, US Ian Gibbons - Portola Valley CA, US Randy McCormick - Santa Clara CA, US
International Classification:
G01N027/26 C12Q001/68 G01N027/447
US Classification:
204/453000, 435/006000, 204/604000
Abstract:
Methods, devices, and systems for unbiased transport of materials on a microfluidic device are disclosed, including methods of maintaining the starting composition of an analyte during transport, and methods of simultaneously analyzing both cationic and anionic components of an analyte. Analyte is loaded into a four-way junction of channels by controlled differential pressure applied to the channels. After analyte loading, an electrical potential is established, forcing charged species into at least one of two separation channels.
M. Goretty Alonso Amigo - Santa Clara CA Randy M. McCormick - Santa Clara CA
Assignee:
ACLARA Biosciences, Inc. - Mountain View CA
International Classification:
G01N 2726 G01N 27447
US Classification:
204454
Abstract:
Electrophoretic chambers having at least a region of surface modification, and methods for their fabrication, are provided. In some embodiments the subject chambers include in the region of surface modification an anchoring polymeric layer interpenetrating the surface of the chamber and an electrophoretic polymeric layer copolymerized with the anchoring polymeric layer. The subject chambers are prepared by sequentially contacting the chamber surface with a first monomer capable of interpenetrating the surface and a second monomer capable of copolymerization with the first monomer, followed by copolymerization of the first and second monomers. In other embodiments an electrophoretic polymeric layer is noncovalently bound on the surface of a rigid polymereic base material without the aid of a separate anchoring polymeric layer. The subject devices find use in any of a variety of electrophoretic applications in which entities are moved through a medium under the influence of an applied electric field.
E. I. Du Pont de Nemours & Company - Wilmington DE
International Classification:
C07H 2100 C07K 318 C07K 320
US Classification:
536 27
Abstract:
The process for separating the proteinaceous materials from nucleic acids involves contacting a solution containing the proteinaceous materials and nucleic acids with a solid phase extraction material capable of binding proteins to form bound and unbound fractions and then isolating the unbound fraction containing the nucleic acids.
Method For Extending The Life Of Electrophoretic Gels
A method for extending the useful lifetime and improving the reproducibility of electrophoresis gels, particularly gel-filled capillaries. The polarity of the applied electric field imposed across the gel is periodically reversed between one or more electrophoretic runs.
Method For Sample Injection In Microchannel Device
Dominic Benvegnu - La Honda CA Randy M. McCormick - Santa Clara CA
Assignee:
Alcara BioSciences, Inc. - Hayward CA
International Classification:
G01N 2726
US Classification:
204453
Abstract:
A method and device are provided for transporting a liquid sample into a third microchannel from an intersection of at least a first, a second, and a fourth microchannel, by stages. In a first stage, liquid sample is moved in and from the fourth microchannel through the intersection and into the second microchannel and concurrently carrier liquid is moved in and from the first and third microchannels through the intersection and into the second microchannel. Thereafter in a second stage, at least part of the contents of the intersection is moved into the third channel and concurrently a part of the contents of the second and fourth microchannels is moved through the intersection and into the third microchannel. Thereafter in a third stage, carrier liquid is moved from the first microchannel simultaneously through the intersection and into the second, third, and fourth microchannels. In some embodiments the liquid sample and the carrier liquid are moved electrokinetically, that is, by application of an electric field to segments of the microchannels.
Methods And Apparatus For Real-Time Monitoring, Measurement And Control Of Electroosmotic Flow
Randy M. McCormick - Santa Clara CA Roy D. Rocklin - Sunnyvale CA
Assignee:
Dionex Corporation - Sunnyvale CA
International Classification:
G01N 2726 G01N 27447
US Classification:
2041801
Abstract:
In capillary electrophoresis systems, real-time monitoring and measurement of the electroosmotic flow through a separation capillary is accomplished by coupling the outlet of the separation capillary to an electrically-conductive junction. In one embodiment, this junction is an ion-impermeable or an ion-exchange membrane unit that preferentially exchanges ions having a charge opposite to analyte ions of interest. Within a downstream region of the junction, all axial incremental voltage from the electroosmotic voltage source is terminated, which ensures that downstream electrolyte ion movement is passive, due to active flow created upstream when an incremental axial voltage existed. Upstream electrolyte ion flux is proportional to C. sub. 1. multidot. (. mu. sub. e +. mu. sub. eo), where C. sub. 1 is the upstream concentration of the electrolyte ion of interest,. mu. sub.
Jonathan Briggs - Los Altos Hills CA Randy M. McCormick - Santa Clara CA David W. Hoyt - Saratoga CA
Assignee:
Seurat Analytical Systems Incorporated - Sunnyvale CA
International Classification:
B01D 5702 B01D 5942 C07K 126 C25B 700
US Classification:
204451
Abstract:
This invention involves method and apparatus for multiplexing electrophoresis analysis. An array of samples in multi well plates are simultaneously transferred to an array of electrophoresis column where electrophoresis is simultaneously carried out followed by analysis of the columns. The methods and apparatus of this invention are, for example, useful for DNA analysis, including sequencing, and for measuring reactions between specifically binding proteins and their binding partners.
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Randy Mccormick
Work:
ViSalus - Director
Education:
Wm. E. Hay Composite High - Stettler, Alberta - High School, Mount Royal College - Arts, University of Calgary - Arts, Articled with intentions of becoming a Charterted Accountant - Commerce, University of Saskatchewan - Funeral Professional
About:
W. R. (Randy) McCormick RNF LBa Born in Stettler, Alberta, I received my training at Mount Royal College and the University of Calgary and since 1962 have been onstage in cities across Canada, served...