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Analogs of ShK Toxin and Their Uses in Selective Inhibition of Kv1.3 Potassium Channels
专利权人:
Bachem Biosciences, Inc.;The Regents of the University of California
发明人:
George K. Chandy,Christine Beeton,William Michael Pennington
申请号:
US13787160
公开号:
US20130274438A1
申请日:
2013.03.06
申请国别(地区):
US
年份:
2013
代理人:
摘要:
Analogs of ShK toxin and methods for using such ShK analogs. The ShK analogs generally comprise ShK toxin attached to a chemical entity (e.g. an atom, molecule, group, residue, compound, moiety, etc.) that has an anionic charge. The ShK analogs may be administered to human or non-human animal subjects to cause inhibition of potassium channels or to otherwise treat diseases or disorders. In some embodiments, the chemical entity to which the ShK toxin is attached may be chosen to provide selective inhibition of certain potassium channels (e.g., Kv1.3 channels) over other potassium channels (e.g., Kv1.1 channels). In come embodiments, the chemical entity to which the ShK toxin is attached may include a fluorophore and such fluorophore-tagged ShK analogs may be used in flow cytometry alone, or in conjunction with class II tetramers that can detect autoreactive cells.
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/

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