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Transposon Vector for Vertebrate & Invertebrate Genetic Manipulation

技术优势
Various types of vectors – introduce transposons to targeted areas in different organisms Successful creation of transgenic animals – genetic transformations in vertebrate and invertebrate cells
技术应用
Research tool for transgenic technology – produce therapeutic proteins or disrupt gene function, e.g. transform mosquito genes to minimize spread of arboviral diseaseGene therapy – alter genes to treat or prevent genetic problems
详细技术说明
None
*Abstract

Background:

Therapeutic delivery of genes is a rapidly evolving technique used to treat or prevent a disease at the root of the problem. The global transgenic market is currently $24B, growing at an annual projected rate of 10%. Currently, a variation of this technique is widely used on animals and crops for production of desirable proteins, but this is a heavily infiltrated market. Thus, entering the gene therapy segment is more promising and would enhance the growth of this industry.

 

Brief Description:

UCR Researchers have identified a novel transposon from Aedes aegypti mosquitoes. This mobile DNA sequence can insert itself into various functional genes to either cause or reverse mutations. They have successfully developed a transposon vector system that can be used in both unicellular & multicellular organisms, which can offer notable insight to improve current transgenic technologies as well as methods of gene therapy.

*Applications
  • Research tool for transgenic technology – produce therapeutic proteins or disrupt gene function, e.g. transform mosquito genes to minimize spread of arboviral disease
  • Gene therapy – alter genes to treat or prevent genetic problems
*IP Issue Date
Oct 17, 2017
*Principal Investigation

Name: Peter Atkinson

Department:


Name: Kun Liu

Department:


Name: Susan Wessler

Department:

申请号码
9790477
其他

Images

Photo by NIH


Tech ID/UC Case

25287/2012-608-0


Related Cases

2012-608-0

国家/地区
美国

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