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Heng Wenling W Zhong, 62419 Brookgreen Dr, Chapel Hill, NC 27516

Heng Zhong Phones & Addresses

419 Brookgreen Dr, Chapel Hill, NC 27516    919-9683388   

703 Cherry Ln, East Lansing, MI 48823   

805 Cherry Ln, East Lansing, MI 48823   

419 Brookgreen Dr, Chapel Hill, NC 27516    919-3507359   

Work

Position: Professional/Technical

Education

Degree: Graduate or professional degree

Emails

Mentions for Heng Wenling W Zhong

Heng Zhong resumes & CV records

Resumes

Heng Zhong Photo 22

Senior Team Lead Ii

Location:
Durham, NC
Industry:
Research
Work:
Syngenta
Senior Team Lead Ii
Michigan State University Apr 1990 - May 1998
Research Associate, Lab Mananger and Cereal Project Leader
Institute of Botany Academy of Science Jul 1989 - Apr 1990
Assistant Professor
Institute of Botany Academy of Science May 1985 - Jul 1989
Research Assistant
Dept of Regulation Biology Faculty of Science Saitama University May 1986 - May 1987
Visiting Scientist
Education:
Institute of Botany
Skills:
Genetics, Biotechnology, Laboratory, Plant Breeding, Cell, In Vitro, Crop, Corn, Molecular Biology, Science
Languages:
English
Mandarin
Heng Zhong Photo 23

Heng Zhong

Work:
United States
Education:
Sichuan University 2012 - 2019
Masters, Electronics Engineering

Publications & IP owners

Us Patents

Methods For Stable Transformation Of Plants

US Patent:
6858777, Feb 22, 2005
Filed:
Aug 13, 2001
Appl. No.:
09/928614
Inventors:
Heng Zhong - Chapel Hill NC, US
Eric Boudreau - Durham NC, US
Sabrina Rouse - Clayton NC, US
Erik Dunder - Hillsborough NC, US
Weining Gu - Chapel Hill NC, US
Yin-Fu Chang - Carrboro NC, US
Assignee:
Syngenta Participations AG - Basel
International Classification:
C12N015/82
C12N015/84
A01H004/00
A01H005/00
US Classification:
800294, 800293, 800298, 800308, 800309, 800310, 800322, 800278, 435430, 435469, 435470, 435431
Abstract:
Multiple shoot structures are induced from plant tissues (e. g. , shoot apices or axillary buds on an artificial medium) to produce multiple shoot cultures. These multi-shoot cultures are then transformed by known transformation methods. Plants are subsequently regenerated from the transformed cells. Crops that may be efficiently transformed by this method include plants normally recalcitrant to transformation such as sugar beet, sunflower, soybean, cotton, tobacco, tomato, peanuts, melons, watermelon, squash, and pepper.

Method For Transforming Soybean (Glycine Max)

US Patent:
2009002, Jan 22, 2009
Filed:
Jul 19, 2007
Appl. No.:
11/880107
Inventors:
Heng Zhong - Chapel Hill NC, US
Qiudeng Que - Cary NC, US
Assignee:
Syngenta Participations AG - Basel
International Classification:
A01H 5/00
C12N 5/04
US Classification:
435415, 800312
Abstract:
The present disclosure provides methods for the transformation of soybean cells or tissue and regeneration of the soybean cells or tissue into transformed plants. The disclosed methods utilize an explant prepared from an immature soybean inflorescence, shoot apex, leaf axillary, shoot axillary, or combination thereof which can be induced directly to form shoots that give rise to transgenic plants via organogenesis.

Transformation Of Sugar Cane

US Patent:
2011032, Dec 29, 2011
Filed:
Dec 1, 2009
Appl. No.:
13/139515
Inventors:
Heng Zhong - Chapel Hill NC, US
International Classification:
C12N 15/82
US Classification:
800293, 435468, 435470, 435469, 800278, 800294
Abstract:
Methods for the transformation of sugar cane are provided. The methods comprise utilizing sugar cane immature shoots as the source of plant material for transformation. Segments of the immature shoot are excised and transformed by any suitable transformation methodology. In some embodiments, the segments are cultured in embryogenic culture induction medium prior to transformation. Transformation can be performed via -mediated gene delivery, biolistic transformation, and the like. Transgenic plants are regenerated from plantlets grown under conditions favoring growth of transformed cells while substantially inhibiting growth of non-transformed cells.

Methods And Compositions For Determination Of Vector Backbone In A Nucleic Acid Sample

US Patent:
2013033, Dec 12, 2013
Filed:
Jun 10, 2013
Appl. No.:
13/913937
Inventors:
- Basel, CH
Chunyang Fan - Research Triangle Park NC, US
John Ke - Research Triangle Park NC, US
Heng Zhong - Research Triangle Park NC, US
Doug Russell - Research Triangle Park NC, US
International Classification:
C12Q 1/68
US Classification:
435 612
Abstract:
The invention provides methods and compositions for detecting and/or quantifying vector backbone in a nucleic acid preparation comprising a polynucleotide of interest using amplification assays that amplify a junction located between the polynucleotide of interest and the vector backbone, under conditions whereby amplification can occur, wherein the junction comprises a recognition site for a nuclease, and detecting the absence of an amplification product, whereby the absence of the amplification product indicates low or no vector backbone and/or quantifying the amount of amplification product to determine the amount of vector backbone in the nucleic acid preparation.

Method For Asexual In Vitro Propagation Of Fertile Corn Plants

US Patent:
5320961, Jun 14, 1994
Filed:
Nov 16, 1992
Appl. No.:
7/977253
Inventors:
Heng Zhong - East Lansing MI
Masomeh B. Sticklen - Okemos MI
Chinnathambi Srinivasan - East Lansing MI
Assignee:
Board of Trustees operating Michigan State University - East Lansing MI
International Classification:
C12N 500
US Classification:
43524045
Abstract:
A method for asexual in vitro propagation of corn plants is described. The plant tissue (shoot tips or apices) are differentiated with 2,4-dichlorophenoxy acetic acid (2,4-D) and N. sup. 6 -benzyladenine (BA) and mixtures thereof and then the differentiated tissue is grown in indole-3-butyric acid (IBA) to produce the corn plant which is fertile.

Method For Producting A Cereal Plant With Foreign Dna

US Patent:
5767368, Jun 16, 1998
Filed:
Apr 3, 1995
Appl. No.:
8/415426
Inventors:
Heng Zhong - East Lansing MI
Masomeh B. Sticklen - Okemos MI
Assignee:
Board of Trustees operating Michigan State University - East Lansing MI
International Classification:
C12N 1529
C12N 1582
A01H 400
A01H 500
US Classification:
800205
Abstract:
A method for isolating a cereal plant with foreign DNA by bombarding meristem primordia tissue with particles coated with the foreign DNA in a culture media is described. The foreign DNA in the transformed plants can provide proteins which impart disease and/or insect resistance or other desirable properties.

Methods Of In Planta Transformation Using Axillary Meristem

US Patent:
2022038, Dec 8, 2022
Filed:
Nov 24, 2020
Appl. No.:
17/775955
Inventors:
- Basel, CH
Wenjin Yu - Research Triangle Park NC, US
Heng Zhong - Research Triangle Park NC, US
Hua-ping Zhou - Research Triangle Park NC, US
Assignee:
SYNGENTA CROP PROTECTION AG - Basel
International Classification:
C12N 15/82
Abstract:
Conventional gene transformation requires tissue culture, and some elite lines have very low transformation efficiency in tissue culture. The disclosure relates to methods of in planta transformation. In some aspects, an axillary meristem of a plant is wounded and contacted with a transformation agent. The wounded axillary meristem is then regenerated and treated with a selection step, resulting in transformed tissue that can produce transgenic seeds.

Targeted Insertion Sites In The Maize Genome

US Patent:
2023011, Apr 13, 2023
Filed:
Aug 26, 2022
Appl. No.:
17/822537
Inventors:
- Basel, CH
Mark Rose - Research Triangle Park NC, US
Zhongying Chen - Research Triangle Park NC, US
Heng Zhong - Research Triangle Park NC, US
Weining Gu - Research Triangle Park NC, US
Wenling Wang - Research Triangle Park NC, US
Qiudeng Que - Research Triangle Park NC, US
Ailing Zhou - Research Triangle Park NC, US
Mary-Dell Chilton - Research Triangle Park NC, US
Assignee:
SYNGENTA PARTICIPATIONS AG - Basel
International Classification:
C12N 15/82
A01H 6/46
Abstract:
The present invention relates to methods and compositions for targeted insertion of polynucleotide molecules into ideal target sites in the genome of a maize plant. The present invention relates to maize recombinant molecules comprising heterologous sequences and also to methods of integrating a DNA of interest into a target maize genomic locus in a maize genome. The present invention also relates to regenerated maize plants or plant parts comprising the recombinant molecules and/or a DNA of interest.

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