Yu Zheng - Melrose MA, US Richard J. Roberts - Wenham MA, US
Assignee:
New England Biolabs, Inc. - Ipswich MA
International Classification:
C12Q 1/00 C12Q 1/68 C12P 21/06
US Classification:
435 4, 435 61, 435 691
Abstract:
Compositions and methods are provided for selection and enrichment of a target gene from a library of polynucleotide sequences such as might be formed from a genome or by random mutagenesis of a genetic sequence. The selection and enrichment occurs in aqueous droplets formed in an emulsion that compartmentalize individual polynucleotides from the library or a plurality of polynucleotides that may include polynucleotides not derived from the library, transcription and translation reagents and optionally additional chemical and enzyme reagents. The selection and enrichment method utilizes a polynucleotide adaptor which when ligated to the polynucleotide fragment enables amplification to occur in the presence of an adaptor specific primer.
Selection And Enrichment Of Proteins Using In Vitro Compartmentalization
Compositions and methods are provided for selection and enrichment of a target gene from a library of polynucleotide sequences such as might be formed from a genome or by random mutagenesis of a genetic sequence. The selection and enrichment occurs in aqueous droplets formed in an emulsion that compartmentalize individual polynucleotides from the library or a plurality of polynucleotides that may include polynucleotides not derived from the library, transcription and translation reagents and optionally additional chemical and enzyme reagents. The selection and enrichment method utilizes a polynucleotide adaptor which when ligated to the polynucleotide fragment enables amplification to occur in the presence of an adaptor specific primer.
Compositions, Methods And Related Uses For Cleaving Modified Dna
Compositions, methods and related uses are provided relating to cleaving modified DNA. For example, a set of DNA fragments obtainable by enzymatic cleavage of a large DNA is described where at least 50% are similarly sized and have a centrally positioned modified nucleotide. In addition, an enzyme preparation is provided that includes one or more enzymes that recognize a modified nucleotide in a DNA and cleave the DNA at a site that is at a non-random distance from the modified nucleotide. The one or more enzymes are further characterized by an N-terminal conserved domain with greater than 90% amino acid sequence homology to WXD(X)YXGD. The related uses include creating a methylome, methods of purifying DNA fragments containing a modified nucleotide and diagnostic applications.
Detection And Quantification Of Hydroxymethylated Nucleotides In A Polynucleotide Preparation
Jurate Bitinaite - Rowley MA, US Romualdas Vaisvila - Ipswich MA, US Sriharsa Pradhan - Wenham MA, US Yu Zheng - Topsfield MA, US Richard J. Roberts - Wenham MA, US Christopher Noren - Boxford MA, US Elisabeth A. Raleigh - Somerville MA, US Geoffrey Wilson - South Hamilton MA, US
Assignee:
NEW ENGLAND BIOLABS, INC. - Ipswich MA
International Classification:
C12Q 1/68
US Classification:
435 611
Abstract:
Methods and compositions are described for detecting hydroxymethylated nucleotides (hmNs) in a polynucleotide preparation with a view to mapping the location of hmNs in a genome, quantifying the occurrence of hmNs at selected loci and correlating the occurrence of hmNs with gene expression and phenotypic traits. Embodiments describe the use of modifying enzymes together with site-specific endonucleases to detect the hmNs.
Compositions, Methods And Related Uses For Cleaving Modified Dna
Yu Zheng - Topsfield MA, US Richard J. Roberts - Wenham MA, US
Assignee:
NEW ENGLAND BIOLABS, INC. - Ipswich MA
International Classification:
C40B 40/06
US Classification:
506 16
Abstract:
Compositions, methods and related uses are provided relating to cleaving modified DNA. For example, a set of DNA fragments obtainable by enzymatic cleavage of a large DNA is described where at least 50% are similarly sized and have a centrally positioned modified nucleotide. In addition, an enzyme preparation is provided that includes one or more enzymes that recognize a modified nucleotide in a DNA and cleave the DNA at a site that is at a non-random distance from the modified nucleotide. The one or more enzymes are further characterized by an N-terminal conserved domain with greater than 90% amino acid sequence homology to WXD(X)YXGD. The related uses include creating a methylome, methods of purifying DNA fragments containing a modified nucleotide and diagnostic applications.
Compositions, Methods And Related Uses For Cleaving Modified Dna
Zhenyu Zhu - Beverly MA, US Yu Zheng - Topsfield MA, US Shengxi Guan - Stoneham MA, US Hua Wang - Topsfield MA, US Aine Quimby - Newton NH, US Penghua Zhang - Lexington MA, US Lynne Apone - Waltham MA, US
Assignee:
NEW ENGLAND BIOLABS, INC. - Ipswich MA
International Classification:
C12Q 1/68 C12N 9/16
US Classification:
435 611, 435196
Abstract:
Compositions, methods and a kit are described relating to a novel family of enzymes which preferentially bind to a hydroxymethylated cytosine or a glucosylated hydroxymethylated cytosine and cleave double-stranded DNA at a defined distance 3′ of the recognition site to produce a cleavage fragment with a 1-3 base overhang.
Detection And Quantification Of Hydroxymethylated Nucleotides In A Polynucleotide Preparation
- Ipswich MA, US Romualdas Vaisvila - Ipswich MA, US Sriharsa Pradhan - Wenham MA, US Yu Zheng - Topsfield MA, US Richard J. Roberts - Wenham MA, US Christopher Noren - Boxford MA, US Elisabeth A. Raleigh - Somerville MA, US Geoffrey Wilson - South Hamilton MA, US
Assignee:
NEW ENGLAND BIOLABS, INC. - Ipswich MA
International Classification:
C12Q 1/68
Abstract:
Methods and compositions are described for detecting hydroxymethylated nucleotides (hmNs) in a polynucleotide preparation with a view to mapping the location of hmNs in a genome, quantifying the occurrence of hmNs at selected loci and correlating the occurrence of hmNs with gene expression and phenotypic traits. Embodiments describe the use of modifying enzymes together with site-specific endonucleases to detect the hmNs.
Leong Leong Architecture New York, NY Dec 2012 to Jan 2013 Intern ArchitectAtelier FCJZ BJ, CN Jul 2011 to Oct 2011 Intern Architect
Education:
Columbia University, Graduate School of Architecture Planning and Preservation New York, NY 2012 to 2013 Master of Science in Architectural DesignSoutheast University, School of Architecture Nanjing, CN 2007 to 2012 Bachelor of Architecture in Architecture
Skills:
AutoCAD / Rhino / Grasshopper / Revit / Maya / 3DMax / Sketchup / Adobe Illustrator / Indesign / Photoshop / Lightroom / After Effects / Premier Pro / Microsoft Office 2011 / Rhino Vray / 3DMax Vray
Name / Title
Company / Classification
Phones & Addresses
Yu Zheng Director, President
601 HUNAN RESTAURANT INC
601 E Mockingbird Ln, Victoria, TX 77904 136 Bowery, New York, NY 10013 39 E Broadway, New York, NY 10002
Yu Zheng Principal
Family Buffet Eating Place
681 Newark Ave, Elizabeth, NJ 07208 (908)3555600
Yu Lai Zheng Secretary, President
China One Yu Inc
11 E Broadway, New York, NY 10038 3720 NW 13 St, Gainesville, FL 32609