Life Technologies since Apr 2010
Senior Staff Scientist
Life Technologies Oct 2008 - Mar 2010
Senior Scientist
LI-COR Biosciences Jan 2004 - Oct 2008
Senior Scientist
LI-COR Biosciences Jul 2001 - Dec 2003
Scientist
Nanjing University of Technology Feb 1991 - Jun 1996
Lecturer
Education:
Case Western Reserve University 1996 - 2001
Ph. D., Chemistry
Nanjing University of Technology 1988 - 1991
MS, Materials Engineering
Nanjing University of Technology 1984 - 1988
BS, Materials Engineering
Skills:
Fluorescence Microscopy Pcr Fluorescence Assay Development Dna Sequencing Dna High Throughput Screening Microscopy Sequencing Genomics Molecular Biology Biotechnology Cell Lifesciences Protein Chemistry Biochemistry Proteomics Protein Purification Genetics Cell Biology Flow Cytometry Hplc Mass Spectrometry Uv/Vis Purification Qpcr Drug Discovery Immunoassays
Xinzhan Peng - Lincoln NE, US Xinshe Xu - Lincoln NE, US Daniel R. Draney - Lincoln NE, US Garrick M. Little - Lincoln NE, US Jiyan Chen - Lincoln NE, US William M. Volcheck - Lincoln NE, US Charles Prescott - Lincoln NE, US
Assignee:
Li-Cor, Inc. - Lincoln NE
International Classification:
C07D 209/56 A61B 5/00
US Classification:
548427, 424 96
Abstract:
The present invention provides for cyanine dyes as near IR quenchers. The cyanine dyes have absorption wavelengths in the near-infrared region of about 650-900 nm and are essentially non-fluorescent. The dyes of the invention have at least one linking group. The present invention also provides substantially non-fluorescent, NIR probes. Biological assays based on these novel, substantially non-fluorescent, NIR probes are also provided.
Theo Nikiforov - Carlsbad CA, US Daniel Mazur - San Diego CA, US Xinzhan Peng - Carlsbad CA, US Yuri Belosludtsev - The Woodlands TX, US Howard Reese - Poway CA, US Dmitriy Gremyachinskiy - Eugene OR, US Roman Rozhkov - Eugene OR, US John M. Mauro - Eugene OR, US Joseph Beechem - Eugene OR, US Eric Tulsky - Eugene OR, US Imad Naasani - Manchester, GB Kari Haley - Eugene OR, US Joseph A. Treadway - Eugene OR, US
Assignee:
Life Technologies Corporation - Carlsbad CA
International Classification:
C12N 9/12
US Classification:
435194, 977773, 514 2
Abstract:
Disclosed herein are conjugates comprising a biomolecule linked to a label that have biological activity and are useful in a wide variety of biological applications. For example, provided herein are polymerase-nanoparticle conjugates including a polymerase linked to a nanoparticle, wherein the conjugate has polymerase activity. Such conjugates can exhibit reduced aggregation and improved stochiometries wherein the average biomolecule:nanoparticle ratio approaches or equals 1:1. Also disclosed herein are improved methods for preparing such conjugates, and methods and systems for using such conjugates in biological applications such as nucleotide incorporation, primer extension and single molecule sequencing.
Xinzhan Peng - Lincoln NE, US Daniel Draney - Lincoln NE, US Jiyan Chen - Lincoln NE, US
Assignee:
LI-COR, Inc. - Lincoln NE
International Classification:
C07D487/22
US Classification:
540/145000
Abstract:
Fluorescent dyes are disclosed which are useful as reporter groups for labeling biomolecules. The silicon phthalocyanine dyes disclosed are preferably water soluble, isomericly pure, possess high quantum yield, and are useful in bioassays.
Methods And Apparatus For Single Molecule Sequencing Using Energy Transfer Detection
JOSEPH BEECHEM - EUGENE OR, US THEO NIKIFOROV - CARLSBAD CA, US Vi-En Choong - Carlsbad CA, US Xinzhan Peng - Carlsbad CA, US Guobin Luo - Oceanside CA, US Cheng-Yao Chen - Carlsbad CA, US Michael Previte - Carlsbad CA, US
Assignee:
LIFE TECHNOLOGIES CORPORATION - CARLSBAD CA
International Classification:
C12Q 1/68 C12N 9/10
US Classification:
435 6, 435193
Abstract:
Provided herein are systems and methods for nucleotide incorporation reactions. The systems comprise polymerases having altered nucleotide incorporation kinetics and are linked to an energy transfer donor moiety, and nucleotide molecules linked with at least one energy transfer acceptor moiety. The donor and acceptor moieties undergo energy transfer when the polymerase and nucleotide are proximal to each other during nucleotide binding and/or nucleotide incorporation. As the donor and acceptor moieties undergo energy transfer, they generate an energy transfer signal which can be associated with nucleotide binding or incorporation. Detecting a time sequence of the generated signals, or the change in the signals, can be used to determine the order of the incorporated nucleotides, and can therefore be used to deduce the sequence of the target molecule.
STEPHEN P. HENDRICKS - LOS GATOS CA, US MICHAEL PHELAN - HAYWARD CA, US MARIAN PERIS - BELMONT CA, US CHENG-YAO CHEN - CARLSBAD CA, US DANIEL MAZUR - SAN DIEGO CA, US XINZHAN PENG - CARLSBAD CA, US AMY CASTILLO - HOUSTON TX, US
Disclosed herein are modified polymerase compositions exhibiting altered polymerase activity, which can be useful in a variety of biological applications. Also disclosed herein are methods of making and using such compositions. In some embodiments, the compositions exhibit altered properties that can enhance their utility in a variety of biological applications. Such altered properties, can include, for example, altered nucleotide binding affinities, altered nucleotide incorporation kinetics, altered photostability and/or altered nanoparticle tolerance, as well as a range of other properties as disclosed herein.
Stephen P. HENDRICKS - Los Gatos CA, US Michael PHELAN - Hayward CA, US Marian PERIS - Belmont CA, US Cheng-Yao CHEN - Carlsbad CA, US Daniel MAZUR - San Diego CA, US Xinzhan PENG - Carlsbad CA, US Amy CASTILLO - Houston TX, US
Disclosed herein are modified polymerase compositions exhibiting altered polymerase activity, which can be useful in a variety of biological applications. Also disclosed herein are methods of making and using such compositions. In some embodiments, the compositions exhibit altered properties that can enhance their utility in a variety of biological applications. Such altered properties, can include, for example, altered nucleotide binding affinities, altered nucleotide incorporation kinetics, altered photostability and/or altered nanoparticle tolerance, as well as a range of other properties as disclosed herein.
Methods And Apparatus For Single Molecule Sequencing Using Energy Transfer Detection
Joseph BEECHEM - Eugene OR, US Theo NIKIFOROV - Carlsbad CA, US Vi-En CHOONG - Carlsbad CA, US Xinzhan PENG - Carlsbad CA, US Guobin LUO - Oceanside CA, US Cheng-Yao CHEN - Carlsbad CA, US Michael PREVITE - Carlsbad CA, US
Assignee:
LIFE TECHNOLOGIES CORPORATION - Carlsbad CA
International Classification:
G01N 21/64
US Classification:
435 61
Abstract:
Provided herein are systems and methods for nucleotide incorporation reactions. The systems comprise polymerases having altered nucleotide incorporation kinetics and are linked to an energy transfer donor moiety, and nucleotide molecules linked with at least one energy transfer acceptor moiety. The donor and acceptor moieties undergo energy transfer when the polymerase and nucleotide are proximal to each other during nucleotide binding and/or nucleotide incorporation. As the donor and acceptor moieties undergo energy transfer, they generate an energy transfer signal which can be associated with nucleotide binding or incorporation. Detecting a time sequence of the generated signals, or the change in the signals, can be used to determine the order of the incorporated nucleotides, and can therefore be used to deduce the sequence of the target molecule.
Library Preparation Methods And Compositions And Uses Therefor
- Carlsbad CA, US Daniel MAZUR - San Diego CA, US Sihong CHEN - Vista CA, US Guobin LUO - Oceanside CA, US Xinzhan PENG - San Diego CA, US
International Classification:
C12N 15/10 C12Q 1/6806 C12Q 1/6853 C12Q 1/6855
Abstract:
Provided are methods for preparing a library of target nucleic acid sequences, as well as compositions and uses therefor. Methods comprise contacting a nucleic acid sample with a plurality of adaptors capable of amplification of one or more target nucleic acid sequences under conditions wherein the target nucleic acid(s) undergo a first amplification; digesting the resulting first amplification products; repairing the digested target amplicons; and amplifying the repaired products in a second amplification, thereby producing a library of target nucleic acid sequence. Each of the plurality of adaptor compositions comprise a handle and a targeted nucleic acid sequence and optionally one or more tag sequences. Provided methods may be carried out in a single, addition only workflow reaction, allowing for rapid production of highly multiplexed targeted libraries, optionally including unique tag sequences. Resulting library compositions are useful for a variety of applications, including sequencing applications.