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Stuart W Tanenbaum

from Morris Plains, NJ
Deceased

Stuart Tanenbaum Phones & Addresses

  • Morris Plains, NJ
  • Whippany, NJ
  • 7472 Armstrong Rd, Manlius, NY 13104 (315) 637-6313
  • Bronx, NY
  • Syracuse, NY
  • Brooklyn, NY
  • New Rochelle, NY

Work

Company: Philip l. kamaras, esq - Brooklyn, NY May 2010 Position: Legal intern

Education

School / High School: Seton Hall University School of Law- Newark, NJ 2009 Specialities: Juris Doctor

Skills

Knowledge of Spanish • Arabi • c and Hebrew • Legal research • computer programming • HTML

Resumes

Resumes

Stuart Tanenbaum Photo 1

Stuart Tanenbaum

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Stuart Tanenbaum Photo 2

Stuart Tanenbaum Beverly Hills, CA

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Work:
Philip L. Kamaras, Esq
Brooklyn, NY
May 2010 to Aug 2010
Legal Intern

John McCain
Arlington, VA
Aug 2008 to Nov 2008
Intern, National Campaign Headquarters

Smith Barney
Beverly Hills, CA
Jun 2007 to Aug 2007
Intern

Education:
Seton Hall University School of Law
Newark, NJ
2009 to 2012
Juris Doctor

Brandeis University
Waltham, MA
2005 to 2008

Skills:
Knowledge of Spanish, Arabi,c and Hebrew, Legal research, computer programming, HTML

Publications

Us Patents

Neuraminidase

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US Patent:
40714080, Jan 31, 1978
Filed:
Nov 1, 1976
Appl. No.:
5/735521
Inventors:
Michael Flashner - Syracuse NY
Stuart W. Tanenbaum - Manlius NY
Assignee:
Research Corporation - New York NY
International Classification:
C12D 1310
US Classification:
195 62
Abstract:
Extracellular neuraminidase (NANAase) is produced by the microorganism Arthrobacter sialophilum sp. nov. The enzyme is induced from this microorganism by a variety of glycoproteins. The preferred enzyme inducer is a hot water extract of edible bird's nest which has been mildly acid-treated. The microorganisms, after aerobic growth in complete medium of relatively simple composition, are harvested, washed, salt-shocked, and induced in mineral salts solution which leads to facile enzyme induction. The produced NANAase is purified by ammonium sulfate fractionation, DEAE cellulose chromatography, gel filtration and ultrafiltration. The enzyme can further be readily crystallized from concentrated solutions. Disc gel electrophoresis at both acidic and basic pH's showed a major protein band. The predominant protein contained NANAase activity.
Stuart W Tanenbaum from Morris Plains, NJDeceased Get Report