Carl Fuller - Berkeley Heights NJ, US Joseph Szasz - Chardon OH, US
Assignee:
Amersham Biosciences Corp - Piscataway NJ
International Classification:
C12Q001/68 C07H021/04
US Classification:
435 6, 536 231, 536 243, 536 2433, 530350
Abstract:
Thermostable DNA polymerases both in native form and having single amino acid substitutions and optionally N-terminal deletions are disclosed. These polymerases exhibit a substantial improvement of DNA sequencing performance compared to Taq DNA polymerase. The instant DNA polymerases also possess improved salt tolerance.
Terminal-Phosphate-Labeled Nucleotides And Methods Of Use
Carl Fuller - Berkeley Heights NJ, US Shiv Kumar - Belle Mead NJ, US Anup Sood - Flemington NJ, US John Nelson - Hillsborough NJ, US
Assignee:
GE Healthcare Bio-Sciences Corp. - Piscataway NJ
International Classification:
C12Q 1/68
US Classification:
435 6
Abstract:
The present invention relates to improved methods of detecting a target using a labeled substrate or substrate analog. The methods comprise reacting the substrate or substrate analog in an enzyme-catalyzed reaction which produces a labeled moiety with independently detectable signal only when such substrate or substrate analog reacts. The present invention, in particular, describes methods of detecting a nucleic acid in a sample, based on the use of terminal-phosphate-labeled nucleotides as substrates for nucleic acid polymerases. The methods provided by this invention utilize a nucleoside polyphosphate, dideoxynucleoside polyphosphate, or deoxynucleoside polyphosphate analogue which has a colorimetric dye, chemiluminescent, or fluorescent moiety, a mass tag or an electrochemical tag attached to the terminal-phosphate. When a nucleic acid polymerase uses this analogue as a substrate, an enzyme-activatable label would be present on the inorganic polyphosphate by-product of phosphoryl transfer. Cleavage of the polyphosphate product of phosphoryl transfer via phosphatase leads to a detectable change in the label attached thereon.
This invention provides methods for massive parallel nucleic acid analysis. A closed complex of nucleic acid template, nucleotide and polymerase can be formed during polymerase reaction, absent divalent metal ion. This is used to trap the nucleotide complementary to the next template nucleotide in the closed complex. Detection of the trapped nucleotide allows determination of the sequence of this next correct nucleotide. In this way, sequential nucleotides of a nucleic acid template can be identified, effectively determining the sequence. This method is applied to sequence multiple templates in parallel, particularly if they are immobilized on a solid support.
Carl W. Fuller - Berkeley Heights NJ, US Cuong Lam - Piscataway NJ, US
Assignee:
GE Healthcare Bio-Sciences Corp. - Piscataway NJ
International Classification:
A61K 38/00 C12Q 1/68 C07K 1/00
US Classification:
530324, 514 2, 530350, 435 6
Abstract:
A purified recombinant DNA polymerase having high processivity and strand-displacement activity. An isolated nucleic acid that encodes the bacteriophage DNA polymerase. A kit and method for amplifying DNA is also disclosed.
Carl W. Fuller - Berkeley Heights NJ, US John R. Nelson - Clifton Park NY, US
Assignee:
GE Healthcare Bio-Sciences Corp. - Piscataway NJ
International Classification:
C12Q 1/68 C07H 21/02 C07H 21/04
US Classification:
435 6, 536 231, 536 243
Abstract:
This invention provides methods for nucleic acid analysis. A closed complex of nucleic acid template, nucleotide and polymerase can be formed during polymerase reaction, absent divalent metal ion. This is used to trap the labeled nucleotide complementary to the next template nucleotide in the closed complex. Detection of the label allows determination of the identity of this next correct nucleotide. Identification can be either in place, as part of the complex, or as the dye is eluted from the complex when the reaction cycle is completed by the addition of divalent metal ion. In this way, sequential nucleotides of a DNA can be identified, effectively determining the DNA sequence. This method can be applied to nucleic acid single molecules or to collections of identical or nearly identical sequence such as PCR products or clones. Multiple templates can be sequenced in parallel, particularly if they are immobilized on a solid support.
Production Of 2',3'-Dideoxy-2',3'-Didehydronucleosides
John E. Starrett - Middletown CT Muzammil M. Mansuri - Cheshire CT John C. Martin - Cheshire CT Carl E. Fuller - Warners NY Henry G. Howell - Jamesville NY
Assignee:
Bristol-Myers Squibb Company - New York NY
International Classification:
C07H 1700 C07H 1906
US Classification:
536 282
Abstract:
There are disclosed novel processes for producing 2',3'-dideoxy-2'3'-didehydronucleosides, for example, 2',3'-dideoxy-2',3'-didehydrothymidine in high yields and on a large scale. The compounds so-produced are useful as antiviral agents, especially as agents effective against the human immunodeficiency viruses (HIV).
Production Of 2',3'-Dideoxy-2',3'-Didehydronucleosides
John E. Starrett - Middletown CT Muzammil M. Mansuri - Cheshire CT John C. Martin - Cheshire CT Carl E. Fuller - Warners NY Henry G. Howell - Jamesville NY
Assignee:
Bristol-Myers Company - New York NY
International Classification:
C07H 1906
US Classification:
536 23
Abstract:
There are disclosed novel processes for producing 2',3'-dideoxy-2'3'-didehydronucleosides, for example, 2',3'-dideoxy-2',3'-didehydrothymidine in high yields and on a large scale. The compounds so-produced are useful as antiviral agents, especially as agents effective against the human immunodeficiency viruses (HIV).
Production Of 2',3'-Dideoxy-2',3'-Didehydronucleosides
John E. Starrett - Middletown CT Muzammil M. Mansuri - Cheshire CT John C. Martin - Cheshire CT Carl E. Fuller - Warners NY Henry G. Howell - Jamesville NY
Assignee:
Bristol-Myers Company - New York NY
International Classification:
C07H 1700
US Classification:
536 23
Abstract:
There are disclosed novel processes for producing 2',3'-dideoxy-2'3'-didehydronucleosides, for example, 2',3'-dideoxy-2',3'-didehydrothymidine in high yields and on a large scale. The compounds so-produced are useful as antiviral agents, especially as agents effective against the human immunodeficiency viruses (HIV).
Name / Title
Company / Classification
Phones & Addresses
Carl Fuller Manager
Shellirae Farm, LLC
Carl F Fuller
CARL FULLER, INC
Carl Fuller
LAKE VISTA INVESTMENTS, LLC
Carl Fuller Manager
G. C. HANFORD MANUFACTURING COMPANY Mfg Pharmaceutical Preparations
304 Oneida St, Syracuse, NY 13202 PO Box 1017, Syracuse, NY 13201 (315)4767418
Fefe Marte, Kevin Aponte, Charina Tatis, Sean Santiago, Ana Guerrero, Kenneth Yeung, Daryl Tejeda, Sheny Rivera, Valerie Rentas, Victoria Sheperd, Dennis Gonzalez
Wainwright Real Estate - Realtor The Real Estate Group - Realtor Prudential Towne Realty - Realtor Century 21 Real Estate (1994-1996)
Relationship:
Married
About:
I, Carl Fuller was originally licensed in NY in 1994 as a Real Estate Agent and worked with Century 21 for 4 years, where I specialized in residential listings and sales. I retired from a NYC civil se...