Company Filing History:
Years Active: 2007-2014
Title: The Innovations of Stefan Russwurm
Introduction
Stefan Russwurm is a notable inventor based in Jena, Germany. He has made significant contributions to the field of biotechnology, particularly in the detection and differentiation of pathophysiological conditions. With a total of 8 patents to his name, Russwurm's work has advanced the understanding of genetic activities and their implications in health.
Latest Patents
One of his latest patents is a method for the in vitro detection and differentiation of pathophysiological conditions. This invention involves using sample nucleic acids to determine gene activities through multiple polynucleotides. It also includes the determination of gene activities of at least one internal reference gene and the formation of an index value from the normalized gene activities of a multigene biomarker, which indicates the pathophysiological condition. Another significant patent is a method for enriching and/or separating prokaryotic DNA using a protein that specifically bonds to unmethylated DNA containing CpG-motifs. This method includes steps for contacting prokaryotic DNA in solution with a specific protein, forming a protein-DNA complex, and subsequently separating the complex. Additionally, this invention is accompanied by a kit designed for its implementation.
Career Highlights
Throughout his career, Stefan Russwurm has worked with several companies, including Sirs-lab GmbH and Analytik Jena AG. His experience in these organizations has allowed him to develop and refine his innovative methods in biotechnology.
Collaborations
Russwurm has collaborated with notable colleagues such as Hans-Peter Deigner and Karl-Hermann Schmidt. Their combined expertise has contributed to the advancement of research in their respective fields.
Conclusion
Stefan Russwurm's contributions to biotechnology through his patents and collaborations highlight his role as a significant inventor in the industry. His innovative methods continue to impact the understanding of genetic activities and their relevance to health conditions.