Joliet School District 86
Bilingual Third Grade Teacher
Kohl Children's Museum 2007 - 2008
Educator
Education:
Thunderbird School of Global Management 1993 - 1995
Master of Business Administration, Masters, Accounting, Finance
The University of Kansas 1986 - 1990
Bachelors, Bachelor of Arts, Latin American Studies, History
Northern Illinois University
Skills:
Classroom Curriculum Design Spanish Teaching Staff Development
Karl Folkers - Austin TX Karl Nils Gunnar Johansson - Austin TX Bruce L. Currie - Austin TX
International Classification:
A61k 2704 A61k 1708
US Classification:
424 1
Abstract:
A method for producing the Folliculotropin Releasing Hormone (FRH) biosynthetically is provided by utilizing, as key starting materials, fresh hypothalamic tissue, a buffered incubation medium, an ATP synthesizing system, radioactively labeled amino acids and a mixture of 21 naturally occuring amino acids. Biosynthesis of the FRH is accomplished by incubation of the hypothalamic tissue for a short period of time in the presence of all the reagents necessary to promote the biosynthetic system to produce the Folliculotropin Releasing Hormone (FRH) of the hypothalamus gland of mammals. Examples of methods to isolate the FRH free of the luteotropin releasing hormone (LRH) are provided.
Synthetic Decapeptide Having The Activity Of The Luteinizing Hormone Releasing Hormone And Method For Manufacturing The Same
Karl Folkers - Austin TX Bruce L. Currie - Austin TX Hans Sievertsson - 191 56 Sollentuna, SW Conny Bogentoft - 19500 Marsta, SW
International Classification:
C07C10352 C07G 700
US Classification:
2601125LH
Abstract:
A synthetic decapeptide, L-pglutamyl-L-histidyl-L-tryptophanyl-L-seryl-L-tyrosyl-glycyl-L-leucyl-L- arginyl-L-prolyl-glycinamide which has the hormonal activities of the luteinizing hormone releasing hormone (LRH) of the hypothalamus gland of mammals is produced by utilizing as the key starting materials, the amino acids, glutamic acid or pyroglutamic acid, histidine, tryptophan, serine, tyrosine, glycine, leucine, arginine, and proline. Synthesis of the decapeptide is accomplished by coupling, in appropriate combinations of appropriate protected forms of the amino acids, and finally deprotecting to yield the amide, L-pglutamyl-L-histidyl-L-tryptophanyl-L-seryl-L-tyrosyl-glycyl-L-leucyl-L- arginyl-L-prolyl-glycinamide.