Shuqi Chen - Brookline MA, US Bertrand Lemieux - Brighton MA, US Zihua Wang - Newton MA, US Kevin R. Kopczynski - Cambridge MA, US Lingjun Chen - Brookline MA, US
A sample processing tubule may include a first segment, a second segment, and a third segment. Each segment may be defined by the tubule, may be fluidly isolated, at least in part by a breakable seal, may be so expandable as to receive a volume of fluid expelled from another segment, and may be so compressible as to contain substantially no fluid when so compressed. Each segment may contain at least one reagent.
A sample processing cartridge may include a plurality of segments arranged in an array at least two rows long and two columns wide. Each segment may be defined by at least one wall of the sample cartridge, fluidly isolated from adjacent segments at least in part by at least one breakable seal or by at least one permanent seal, so expandable as to receive a volume of fluid expelled from another segment, and so compressible as to contain substantially no fluid when so compressed. At least two adjacent segments of at least one row of the array may be aligned along a longitudinal axis of the row and have substantially the same height along a latitudinal axis of the row. At least two adjacent segments in at least one row may be separated by a permanent seal to form at least two tracks. At least one segment, or at least two adjacent segments separated by a breakable seal, may be in fluid communication with the at least two tracks. At least one segment may contain at least one reagent.
A sample processing vessel may include a branch segment and at least two tracks. The at least two tracks may be fluidly isolated from one another by a permanent seal. The tracks may be segmented by breakable seals. The branch segment may be temporarily isolated from the tracks by breakable seal(s) and put in fluid communication with the tracks once those seal(s) are broken, such that fluid received by the branch segment is divided into portions that pass into both tracks.
Biohelix since Feb 2006
S. Director for Technology
IQuum Inc. Sep 2002 - Feb 2006
Director Technology Innovation
University of Delaware Sep 1997 - Sep 2002
Professor
York University Jul 1990 - Aug 1997
Associate Professor / Assistant Professor
Education:
Michigan State University 1988 - 1990
Post doctoral, Plant biochemistry
Laval University 1986 - 1988
PhD, Molecular Genetics
Laval University 1984 - 1986
Master of Science (M.S.), Molecular Biology
Université Laval 1981 - 1984
Bachelor of Science (B.S.), Biochemistry
Skills:
Molecular Biology Lifesciences Biochemistry Biotechnology Pcr R&D Medical Devices Dna Infectious Diseases Genomics Data Analysis Bioinformatics Research Microbiology Cell Biology Cell Culture Project Management Microsoft Office Commercialization
2006 to 2000 Senior Director for Technology DevelopmentIQuum Inc Allston, MA Aug 2002 to Feb 2006 Director of InnovationUniversity of Delaware Newark, DE Sep 1997 to Aug 2002 ProfessorYork University Toronto, ON Jul 1990 to Jul 1997 Associate Professor & Assistant Professor
Education:
Laval University Qubec, QC 1986 to 1988 PhD. in Molecular GeneticsLaval University Qubec, QC 1984 to 1986 M.S. in Molecular BiologyLaval University Qubec, QC 1981 to 1984 B.S. in Biochemistry
Skills:
Business Development (bid & proposal and market research), Intellectual Property research, laboratory management, editorial review, science writing