U.S. Air Force Tyndall AFB, FL Mar 2014 to Nov 2014 Aerospace and Operational Physiology Flight CommanderU.S. Air Force Tyndall AFB, FL Aug 2013 to Mar 2014 Director, Aerospace and Operational PhysiologyU.S. Air Force Andrews AFB, MD Aug 2012 to Aug 2013 Chief, Human Factors Safety Division, Air National GuardU.S. Air Force Andrews AFB, MD Jun 2010 to Jul 2012 Chief of Flight Safety, Air Force District of Washington (AFDW)U.S. Air Force Andrews AFB, MD Aug 2009 to Jun 2010 Aerospace and Operational Physiology Flight CommanderU.S. Air Force Andrews AFB, MD Aug 2006 to May 2008 Aerospace and Operational Physiology Training Flight Deputy CommanderU.S. Air Force Wright-Patterson AFB, OH Aug 2003 to Jul 2006 Program Manager, Spatial Disorientation (SD) CountermeasuresU.S. Air Force Elmendorf AFB, AK Aug 2000 to Aug 2003 Chief, Aerospace Physiology (AP) Human Performance Training Team (HPTT)U.S. Air Force Elmendorf AFB, AK Aug 2000 to Aug 2003 Military Conservation AgentU.S. Air Force Sheppard AFB, TX Mar 1997 to Aug 2000 Chief, Aerospace Physiology Standardization and EvaluationU.S. Air Force Malmstrom AFB, MT Aug 1995 to Mar 1997 In-Flight Refueling Technician
Education:
Air University Maxwell AFB, AL 2012 Air Command and Staff College (Correspondence)Embry-Riddle Aeronautical University 2011 Master of Aeronautical Science in Human Factors in Aerospace Systems and Aerospace SafetyAir University Maxwell AFB, AL 2006 Squadron Officer School (Correspondence)Community College of the Air Force Maxwell AFB, AL 1997 Associate of Science in Aircrew OperationsEmbry-Riddle Aeronautical University Prescott, AZ 1994 Bachelor of Science in Aerospace Studies (Aviation Safety, Aviation Business Administration, and Human Factors Psychology)
Military:
Rank: Major Jan 1995 to Jan 2015 Branch: U.S. Air ForceL.i.location.original
QinetiQ-North America Huntsville, AL Dec 2006 to Jun 2013 Program Manager Software DevelopmentWestar A&DG Huntsville, AL Jul 2004 to Nov 2006 Network Security Program ManagerNon-Appropriated Funds Fort Campbell, KY Jul 2000 to Jun 2004 Computer SpecialistUnited States Army
Sep 1980 to Oct 2000 Personnel Management/Aviation Logistics/Information Technology
Education:
Strayer University Nashville, TN Jun 2005 MBAAustin Peay State University Clarksville, TN 2000 to 2002 BS in Public Administration
Military:
Rank: SFC/E-7 Sep 1980 to Oct 2000 Branch: US ArmyL.i.location.original
Skills:
Logistics Management, Windows O/S Adminstration, Network Configuration, Network Security. MS Office Administration, Team Foundation Server, Help Desk Support.
Lei Young - Rockville MD, US Hamilton O. Smith - Reisterstown MD, US Daniel Glenn Gibson - Crofton MD, US
Assignee:
Synthetic Genomics, Inc. - San Diego CA
International Classification:
C12P 19/34 C12N 9/00 C12N 15/00
US Classification:
435 911, 435183, 435440
Abstract:
The present invention relates, e. g. , to in vitro method, using isolated protein reagents, for joining two double stranded (ds) DNA molecules of interest, wherein the distal region of the first DNA molecule and the proximal region of the second DNA molecule share a region of sequence identity, comprising contacting the two DNA molecules in a reaction mixture with (a) a non-processive 5′ exonculease; (b) a single stranded DNA binding protein (SSB) which accelerates nucleic acid annealing; (c) a non strand-displacing DNA polymerase; and (d) a ligase, under conditions effective to join the two DNA molecules to form an intact double stranded DNA molecule, in which a single copy of the region of sequence identity is retained. The method allows the joining of a number of DNA fragments, in a predetermined order and orientation, without the use of restriction enzymes.
Daniel Glenn Gibson - Crofton MD, US Hamilton O. Smith - Reisterstown MD, US
Assignee:
Synthetic Genomics, Inc. - San Diego CA
International Classification:
C12Q 1/68 C12P 19/34 C07H 21/02 C07H 21/04
US Classification:
435 6, 435 912, 536 231, 536 243
Abstract:
The present invention relates, e. g. , to an in vitro method, using isolated protein reagents, for joining two double-stranded (ds) DNA molecules of interest, wherein the distal region of the first DNA molecule and the proximal region of the second DNA molecule share a region of sequence identity, comprising (a) chewing back the DNA molecules with an enzyme having an exonuclease activity, to yield single-stranded overhanging portions of each DNA molecule which contain a sufficient length of the region of sequence identity to hybridize specifically to each other; (b) specifically annealing the single-stranded overhangs; and (c) repairing single-stranded gaps in the annealed DNA molecules and sealing the nicks thus formed (ligating the nicked DNA molecules). The region of sequence identity generally comprises at least 20 non-palindromic nucleotides (nt), e. g. , at least about 40 non-palindromic nt.
Daniel Glenn Gibson - Crofton MD, US Hamilton O. Smith - San Diego CA, US
Assignee:
Synthetic Genomics, Inc. - La Jolla CA
International Classification:
C12Q 1/68 C12P 19/34 C07H 21/02 C07H 21/04
US Classification:
435 61, 435 912, 536 231, 536 243
Abstract:
The present invention relates to an in vitro method, using isolated protein reagents, for joining two double-stranded (ds) DNA molecules of interest, wherein the distal region of the first DNA molecule and the proximal region of the second DNA molecule share a region of sequence identity. The method allows the joining of a number of DNA fragments, in a predetermined order and orientation, without the use of restriction enzymes. It can be used, e. g. , to join synthetically produced sub-fragments of a gene or genome of interest.
Direct Extrusion Method For The Fabrication Of Photonic Band Gap (Pbg) Fibers And Fiber Preforms
Daniel J. Gibson - Cheverly MD, US Jasbinder S. Sanghera - Ashburn VA, US Frederic H. Kung - Alexandria VA, US Pablo C Pureza - Burke VA, US Robert E Miklos - La Plata MD, US Guillermo R. Villalobos - Springfield VA, US Leslie Brandon Shaw - Woodbridge VA, US Ishwar D. Aggarwal - Charlotte NC, US
Assignee:
The United States of America as represented by the Secretary of the Navy - Washington DC
International Classification:
G02B 6/032
US Classification:
385125
Abstract:
A method and apparatus for making a substantially void-free preform for a microstructured optical fiber using a one-step process is provided. A preform is prepared from specialty glasses using a direct extrusion method. A die for use with the direct extrusion method is also provided, and a method for drawing the preform into a HC-PBG fiber for use in transmitting infra-red wavelength light is also provided. The preform comprises an outer jacket made of solid glass, a cladding having a plurality of air holes arranged in a desired pattern within the jacket, and a core which is hollow.
Daniel G. Gibson - Crofton MD, US Lei Young - Gaithersburg MD, US John I. Glass - Germantown MD, US Gwynedd A. Benders - San Diego CA, US J. Craig Venter - La Jolla CA, US Hamilton O. Smith - San Diego CA, US
Assignee:
Synthetic Genomics, Inc. - La Jolla CA
International Classification:
C12P 19/34 C12N 1/19 C07H 21/04
US Classification:
435 911, 4352542, 536 231
Abstract:
A method to assemble any desired nucleic acid molecule by combining cassettes in vitro to form assemblies which are further combined in vivo, or by assembling large numbers of DNA fragments by recombination in a yeast culture to obtain desired DNA molecules of substantial size is described.
Methods For In Vitro Joining And Combinatorial Assembly Of Nucleic Acid Molecules
Daniel G. GIBSON - Crofton MD, US Hamilton O. SMITH - San Diego CA, US Clyde A. HUTCHISON - La Jolla CA, US Lei YOUNG - Gaithersburg MD, US J. Craig VENTER - La Jolla CA, US
International Classification:
C12P 19/34 C40B 40/08 C07H 21/04
US Classification:
506 17, 435 912, 536 231
Abstract:
The present invention relates to methods of joining two or more double-stranded (ds) or single-stranded (ss) DNA molecules of interest in vitro, wherein the distal region of the first DNA molecule and the proximal region of the second DNA molecule of each pair share a region of sequence identity. The method allows the joining of a large number of DNA fragments, in a predetermined order and orientation, without the use of restriction enzymes. It can be used, e.g., to join synthetically produced sub-fragments of a gene or genome of interest. Kits for performing the method are also disclosed. The methods of joining DNA molecules may be used to generate combinatorial libraries useful to generate, for example, optimal protein expression through codon optimization, gene optimization, and pathway optimization.
Lei YOUNG - Gaithersburg MD, US Hamilton O. Smith - San Diego CA, US Daniel Glenn Gibson - Crofton MD, US
International Classification:
C12N 9/12
US Classification:
435194
Abstract:
The present invention relates, e.g., to in vitro method, using isolated protein reagents, for joining two double stranded (ds) DNA molecules of interest, wherein the distal region of the first DNA molecule and the proximal region of the second DNA molecule share a region of sequence identity, comprising contacting the two DNA molecules in a reaction mixture with (a) a non-processive 5′ exonuclease; (b) a single stranded DNA binding protein (SSB) which accelerates nucleic acid annealing; (c) a non strand-displacing DNA polymerase; and (d) a ligase, under conditions effective to join the two DNA molecules to form an intact double stranded DNA molecule, in which a single copy of the region of sequence identity is retained. The method allows the joining of a number of DNA fragments, in a predetermined order and orientation, without the use of restriction enzymes.
Daniel J. Gibson - Greenbelt MD, US Jasbinder S. Sanghera - Ashburn VA, US Frederic H. Kung - Alexandria VA, US Ishwar D. Aggarwal - Fairfax Station VA, US
Assignee:
The Government of the United States of America, as represented by the Secretary of the Navy - Washington DC
International Classification:
G02B 6/032 G02B 6/036 C03B 37/02 C03B 37/075
US Classification:
385125, 385128, 65393
Abstract:
A method and apparatus for making a substantially void-free microstructured optical fiber using a one-step process is provided. A preform for the optical fiber is prepared, comprising an outer jacket made of solid glass, a cladding having a plurality of microtubes and/or microcanes arranged in a desired pattern within the jacket, and a core which may be solid or hollow, with the cladding and the core extending above the top of the outer jacket. The thus-prepared preform is placed into a fiber draw tower. As the fiber is drawn, negative gas pressure is applied to draw the canes together and consolidate the interfacial voids between the canes while positive gas pressure is applied to the preform to keep the holes of the microcanes open during the fiber drawing. The apparatus includes a jig having support tubes that are connected to a vacuum pump for application of the negative gas pressure and a vent tube connected to a gas supply for application of the positive gas pressure. The interfaces between the support tube and the outer jacket and between the vent tube and the cladding are sealed to ensure that the appropriate application of negative or positive pressure during the draw step is obtained. The preforms according to the present invention can include one or more components fabricated from specialty non-silica glass.
Capital Region Medical ClinicCapital Region Health Branch West 3308 W Edgewood Dr STE B, Jefferson City, MO 65109 573 893-7848 (phone), 573 893-1984 (fax)
Capital Region Medical ClinicCapital Region Physicians Urgent Care 220 Madison St, Jefferson City, MO 65101 573 632-4900 (phone), 573 644-6650 (fax)
Education:
Medical School Oklahoma State University Center for Health Sciences College of Osteopathic Medicine Graduated: 1999
Procedures:
Allergen Immunotherapy Electrocardiogram (EKG or ECG) Vaccine Administration Wound Care
Dr. Gibson graduated from the Oklahoma State University Center for Health Sciences College of Osteopathic Medicine in 1999. He works in Jefferson City, MO and 1 other location and specializes in Family Medicine and Urgent Care Medicine. Dr. Gibson is affiliated with Capital Region Medical Center.