Sandstone Diagnostics Inc. since Jul 2012
Chief Technology Officer
Sandia National Laboratories Feb 2010 - Jul 2012
Postdoctoral Appointee
University of California, Davis Jun 2007 - Feb 2010
Post-Doc
UC Davis Jan 2004 - Jun 2007
Graduate Student Researcher/Lab Manager
UC Davis May 2005 - May 2007
Graduate fellow
Education:
University of California, Davis 2003 - 2007
Doctor of Philosophy (Ph.D.), Bioengineering and Biomedical Engineering
University of California, San Diego 2001 - 2002
MEng, Bioengineering
University of California, Berkeley 1997 - 2001
B.S., Bioengineering
Skills:
Fluorescence Microscopy Biomedical Engineering Assay Development Microfluidics Microscopy Cell Culture Flow Cytometry Fluorescence Elisa Confocal Microscopy Troubleshooting Optical Fiber Spectroscopy R&D Life Sciences Dna Laboratory Molecular Biology In Vitro
Chief Technology Officer at Sandstone Diagnostics Inc.
Location:
San Francisco Bay Area
Industry:
Biotechnology
Work:
Sandstone Diagnostics Inc. since Jul 2012
Chief Technology Officer
Sandia National Laboratories Feb 2010 - Jul 2012
Postdoctoral Appointee
University of California, Davis Jun 2007 - Feb 2010
Post-Doc
UC Davis Jan 2004 - Jun 2007
Graduate Student Researcher/Lab Manager
UC Davis May 2005 - May 2007
Graduate fellow
Education:
University of California, Davis 2003 - 2007
Doctor of Philosophy (Ph.D.), Bioengineering and Biomedical Engineering
University of California, San Diego 2001 - 2002
MEng, Bioengineering
University of California, Berkeley 1997 - 2001
B.S., Bioengineering
- Albuquerque NM, US Ulrich Y. Schaff - Livermore CA, US Gregory J. Sommer - Livermore CA, US
International Classification:
B01L 3/00 G01N 15/04 G01N 33/543
Abstract:
Embodiments of the present invention are directed toward devices, systems, and method for conducting nucleic acid purification and quantification using sedimentation. In one example, a method includes generating complexes which bind to a plurality of beads in a fluid sample, individual ones of the complexes comprising a nucleic acid molecule such as DNA or RNA and a labeling agent. The plurality of beads including the complexes may be transported through a density media, wherein the density media has a density lower than a density of the beads and higher than a density of the fluid sample, and wherein the transporting occurs, at least in part, by sedimentation. Signal may be detected from the labeling agents of the complexes.
Toxin Activity Assays, Devices, Methods And Systems Therefor
- Albuquerque NM, US Ulrich Y. Schaff - Livermore CA, US Gregory Jon Sommer - Livermore CA, US
International Classification:
G01N 33/53
Abstract:
Embodiments of the present invention are directed toward devices, system and method for conducting toxin activity assay using sedimentation. The toxin activity assay may include generating complexes which bind to a plurality of beads in a fluid sample. The complexes may include a target toxin and a labeling agent, or may be generated due to presence of active target toxin and/or labeling agent designed to be incorporated into complexes responsive to the presence of target active toxin. The plurality of beads including the complexes may be transported through a density media, wherein the density media has a lower density than a density of the beads and higher than a density of the fluid sample, and wherein the transporting occurs, at least in part, by sedimentation. Signal may be detected from the labeling agents of the complexes.
Quantitative Detection Of Pathogens In Centrifugal Microfluidic Disks
- Albuquerque NM, US Ulrich Y. Schaff - Livermore CA, US Gregory Jon Sommer - Maple Grove MN, US
International Classification:
C12Q 1/68
Abstract:
A system and methods for detection of a nucleic acid including forming a plurality of nucleic acid detection complexes are described, each of the complexes including a nucleic acid analyte, a detection agent and a functionalized probe. The method further including binding the nucleic acid detection complexes to a plurality of functionalized particles in a fluid sample and separating the functionalized particles having the nucleic acid detection complexes bound thereto from the fluid sample using a density media. The nucleic acid analyte is detected by detecting the detection agent.
Devices, Systems, And Methods For Conducting Assays With Improved Sensitivity Using Sedimentation
Ulrich Y. SCHAFF - Livermore CA, US Chung-Yan Koh - Dublin CA, US Gregory J. Sommer - Livermore CA, US
International Classification:
G01N 33/53 B82Y 15/00
US Classification:
436501, 422 69, 977774, 977902
Abstract:
Embodiments of the present invention are directed toward devices, systems, and method for conducting assays using sedimentation. In one example, a method includes layering a mixture on a density medium, subjecting sedimentation particles in the mixture to sedimentation forces to cause the sedimentation particles to move to a detection area through a density medium, and detecting a target analyte in a detection region of the sedimentation channel. In some examples, the sedimentation particles and labeling agent may have like charges to reduce non-specific binding of labeling agent and sedimentation particles. In some examples, the density medium is provided with a separation layer for stabilizing the assay during storage and operation. In some examples, the sedimentation channel may be provided with a generally flat sedimentation chamber for dispersing the particle pellet over a larger surface area.