Dr. West graduated from the St Matthew's Univ Grand Cayman in 2005. He works in Saraland, AL and specializes in Family Medicine. Dr. West is affiliated with Mobile Infirmary Medical Center.
Dr. West graduated from the Des Moines University College of Osteopathic Medicine in 1997. He works in Wheat Ridge, CO and specializes in Family Medicine. Dr. West is affiliated with Lutheran Medical Center and St Joseph Hospital.
Dr. West works in Grants Pass, OR and specializes in Cardiovascular Disease. Dr. West is affiliated with Asante Rogue Regional Medical Center and Asante Three Rivers Medical Center.
Aug 2011 to 2000 Director of Multicultural AffairsWalsh University
Aug 2011 to 2000 Social and Behavioral Sciences Graduate Assistant
Education:
Walsh University North Canton, OH 2007 to 2011 Bachelor of Arts in Psychology and SociologyWalsh University North Canton, OH 2016 Masters of Arts in Counseling and Human Development
Military:
Rank: AZ3 May 1991 to Jun 1995 Branch: NavyL.i.location.original
MG Transport, LLC Portland, OR Aug 2012 to Oct 2012 Truck DriverGordon Trucking, Inc Pacific, WA Jun 2012 to Aug 2012 Truck DriverTerrill Transportation Manteca, CA Oct 2010 to Jun 2012 Truck DriverTiger Lines, LLC Lodi, CA Apr 2008 to Oct 2010 Truck DriverSystem Transport Spokane, WA Mar 2007 to Mar 2007 Truck DriverExpress Personnel Stockton, CA Sep 2006 to Jan 2007 Temporary Warehouse WorkerJensen Precast Lockeford, CA Apr 2005 to Aug 2006 Yard ForemanExpress Personnel Stockton, CA Feb 2005 to Apr 2005 Temporary Laborer
Education:
Mt Diablo Adult Education Concord, CA 1993 to 1993 High School Diploma
2007 to 2000 Production Manager / Graphic DesignerLogo Graphics St. Louis, MO 2006 to 2010 Graphic Designer / FreelanceLogo Graphics St. Louis, MO Jan 2009 to May 2009 Artist in Residence / TeacherAllstar Solutions St. Louis, MO 2006 to 2007 Graphic Designer
Education:
Fontbonne University St. Louis, MO 2005 Bachelor of Fine Arts in Fine Arts / Graphic Design
Skills:
Graphic Design, Apparel Design, Web Development
Name / Title
Company / Classification
Phones & Addresses
Jason West Officer
United Bio Source Corp Computer Programming Services
55 Francisco St # 780, San Francisco, CA 94133 Website: dynarand.com
Jason West CTO
Dynarand LLC Computer Integrated Systems Design
55 Francisco St Ste 780, San Francisco, CA 94133
Jason West Outreach Supervisor
Medicann Inc Health and Allied Services
1814 Franklin St Ste 901, Oakland, CA 94612
Jason West Manager
Mullinax Ford N Canton Inc Motor Vehicle Dealers (New and Used)
Jason West - Castro Valley CA, US James Stamps - Livermore CA, US Isaac Shokair - Livermore CA, US Ronald Renzi - Tracy CA, US Victoria Vandernoot - Pleasanton CA, US Boyd Wiedenman - Alpharetta GA, US Todd Lane - Livermore CA, US Julia Fruetel - Livermore CA, US
The present invention provides systems and processes for the collection and identification of macromolecules, such as biologically-derived macromolecules (e.g., proteins and nucleic acids), by measuring and comparing the molecular weight signatures of macromolecular samples. Reproducible molecular weight signatures provides reliable sample identification. In the case of viruses, proteomic molecular weight signatures can be used for identifying viral agents.
Microfluidic Integrated Microarrays For Biological Detection
Jason West - Castro Valley CA, US Timothy Shepodd - Livermore CA, US Stewart Griffiths - Livermore CA, US Ronald Renzi - Tracy CA, US Boyd Wiedenman - Alpharetta GA, US
International Classification:
C12Q001/68 C12M001/34
US Classification:
435006000, 435287200, 435288500
Abstract:
Disclosed are microflulidic chips that include a plurality of vias; a functionalized porous polymer monolith capable of being in fluid communication with a via; a microarray capable of being in fluid communication with the functionalized porous polymer monolith; and an observation port through which at least one target disposed within the microarray is capable of being detected. The disclosed microfluidic chips contain microarrays that can be effectively coupled to functionalized porous polymer monoliths for capturing and concentrating sample nucleic acids. Also disclosed are microfluidic chips containing microarray probes having observation ports that enable the preparation of microarrays and the detection of targets. These microfluidic chips are capable of capturing and concentrating genetic material for the analysis and identification of biological organisms, such as so-called “threat genes” from chimeric bioweapons.
Systems And Methods For Effecting A Physical Change In A Biological Sample
Kyle W. Hukari - San Ramon CA, US Jason A.A. West - Castro Valley CA, US
International Classification:
C12Q 1/00 C12M 3/00
US Classification:
435 4, 4352871
Abstract:
The present invention relates generally to systems and methods for processing a biological sample that result in a physical change, such as reacting two molecules together to form a reaction product or for use in lysing viruses or biological cells for analysis using biological assay systems. As such, the present invention relates both to breaking apart biological species such as viruses and cells, as well as the formation of reactants from one or more reactive species. The sample has a volume in the range from about 1 microliter to 10 milliliters. The sample is processed by applying pressure, and either sonic energy or thermal energy to the sample, wherein the pressure achieved is usually at least 24 atmospheres, and the temperature of the sample is usually raised to at least 50 C.
Kyle W. Hukari - Dublin CA, US Jason A.A. West - Pleasanton CA, US
Assignee:
ARCXIS BIOTECHNOLOGIES - Pleasanton CA
International Classification:
C12N 13/00 C12N 5/00 C12M 1/02
US Classification:
4351731, 435325, 4353061
Abstract:
The present invention relates generally to systems and methods for processing a biological sample that result in a physical change, such as reacting two molecules together to form a reaction product or for use in lysing viruses or biological cells for analysis using biological assay systems. As such, the present invention relates both to breaking apart biological species such as viruses and cells, as well as the formation of reactants from one or more reactive species. The sample has a volume in the range from about 1 microliter to 10 milliliters. The sample is processed by applying pressure, and either sonic energy or thermal energy to the sample, wherein the pressure achieved is usually at least 24 atmospheres, and the temperature of the sample is usually raised to at least 50 C.
Kyle W. Hukari - Dublin CA, US Jason A.A. West - Pleasanton CA, US Michael A. Shultz - Bend OR, US Richard Milson - Citrus Heights CA, US Nikolas M. Isely - Moraga CA, US Michael C. DeRenzi - San Ramon CA, US
International Classification:
C12M 1/12 C12N 5/071
US Classification:
435325, 4353061
Abstract:
Provided are cartridges and systems for effecting automated extraction, isolation, and purification of cellular components—such as nucleic acids—from a cellular sample in assay-ready form. Also provided are related methods of effecting such sample processing.
Provided are microfluidic devices and methods for fabricating and bonding such devices. Also provided are kits for analyzing analyte-containing samples and for lysing cells.
Methods, Systems And Devices For Multiple Single-Cell Capturing And Processing Using Microfluidics
Jake Kimball - Oakland CA, US Myo Thu Maung - Brisbane CA, US Andrew May - San Francisco CA, US Michael C. Norris - Mountain View CA, US Dominique G. Toppani - Oakland CA, US Marc A. Unger - San Mateo CA, US Jing Wang - Daly City CA, US Jason A.A. West - Pleasanton CA, US
International Classification:
C12Q 1/68
US Classification:
435 34, 435174, 435 912
Abstract:
Methods, systems, and devices are described for multiple single-cell capturing and processing utilizing microfluidics. Tools and techniques are provided for capturing, partitioning, and/or manipulating individual cells from a larger population of cells along with generating genetic information and/or reactions related to each individual cell. Different capture configurations may be utilized to capture individual cells and then processing each individual cell in a multi-chamber reaction configuration. Some embodiments may provide for specific target amplification, whole genome amplification, whole transcriptome amplification, real-time PCR preparation, copy number variation, preamplification, mRNA sequencing, and/or haplotyping of the multiple individual cells that have been partitioned from the larger population of cells. Some embodiments may provide for other applications. Some embodiments may be configured for imaging the individual cells or associated reaction products as part of the processing. Reaction products may be harvested and/or further analyzed in some cases.
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