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Kazuko Aoyagi

from Princeton, NJ
Age ~73

Kazuko Aoyagi Phones & Addresses

  • 46 Caleb Ln, Princeton, NJ 08540 (609) 356-0072 (609) 356-0073
  • 80 Jackson Ave, Princeton, NJ 08540 (609) 683-1254 (609) 683-5957 (609) 683-9766
  • 702 Blue Spring Rd, Princeton, NJ 08540 (609) 683-9766
  • Emeryville, CA
  • Walnut Creek, CA
  • 10 Rogers St, Cambridge, MA 02142
  • Lafayette, CA
  • 46 Caleb Ln, Princeton, NJ 08540 (609) 731-9228

Work

Company: Us-japan health care study group 2010 Address: Greater New York City Area Position: Vice president

Education

School / High School: Massachusetts Institute of Technology 2000 to 2001 Specialities: pharmacology, molecular medicine

Awards

Fulbright scholarship 1981-87

Industries

Research

Resumes

Resumes

Kazuko Aoyagi Photo 1

Director

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Position:
Vice President at US-Japan Health Care Study Group, Member at Regulatory Harmonization Institute, Director, Business Development, ESD and BAS at Celerion Inc, vice president at Princeton Japanese Association, Member at New York Pharma Forum, Central NJ director at WITS
Location:
Greater New York City Area
Industry:
Research
Work:
US-Japan Health Care Study Group - Greater New York City Area since 2010
Vice President

Regulatory Harmonization Institute since Dec 2010
Member

Celerion Inc since Apr 2010
Director, Business Development, ESD and BAS

Princeton Japanese Association - Princeton, NJ since 2007
vice president

New York Pharma Forum since 2002
Member
Education:
Massachusetts Institute of Technology 2000 - 2001
University of California, Berkeley 1981 - 1985
PhD, Plant molecular biology
Honor & Awards:
Fulbright scholarship 1981-87

Publications

Us Patents

Methods Using Exogenous, Internal Controls And Analogue Blocks During Nucleic Acid Amplification

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US Patent:
59522020, Sep 14, 1999
Filed:
Mar 26, 1998
Appl. No.:
9/048880
Inventors:
Kazuko Aoyagi - Emeryville CA
Kenneth J. Livak - San Jose CA
Assignee:
The Perkin Elmer Corporation - Foster City CA
International Classification:
C12P 1934
C12Q 168
C07H 2104
US Classification:
435 912
Abstract:
Reporter-quencher probe assays of nucleic acid amplification, such as PCR, are rendered more meaningful by the addition of internal control reagents. An internal control polynucleotide is amplified with internal control primers and the product is measured by correlation with increased fluorescence by polymerase mediated-exonuclease cleavage or hybridization of the internal control probe. Probes specific for target and internal control polynucleotides are labelled with spectrally resolvable reporters, allowing for concurrent detection and measurement of target and control amplification. A kit of all PCR reagents can be dispensed into reaction chambers in a high-throughput system for rapid and accurate nucleic acid amplification assay, with real-time or end-point measurements. Fluorescent signals correlated to target and internal control levels are spectrally resolvable and measured concurrently. A non-extending oligonucleotide or nucleic analog "block", complementary to the internal control polynucleotide, is added to the amplification mixture to preclude amplification of the internal control polynucleotide and function as an internal negative control.
Kazuko Aoyagi from Princeton, NJ, age ~73 Get Report