Method for assaying compounds or agents for ability to displace potent ligands of hematopoietic prostaglandin D synthase
申请人:Palackal Nisha
公开号:US08440417B2
公开(公告)日:2013-05-14
An exemplary embodiment may be directed to a fluorescence polarization assay that screens compounds or agents for their affinity to hematopoietic prostaglandin D synthase (H-PGDS) based on their ability to displace a fluorophore-containing detection analyte bound to an enzyme comprising the primary amino acid sequence of H-PGDS. Another exemplary embodiment utilizes an enzyme having a maltose binding protein amino-acid sequence fused with an N-terminus of the enzyme.
METHODS FOR ASSAYING COMPOUNDS OR AGENTS FOR ABILITY TO DISPLACE POTENT LIGANDS OF HEMATOPOIETIC PROSTAGLANDIN D SYNTHASE
申请人:Cayman Chemical Company
公开号:EP2286221A2
公开(公告)日:2011-02-23
US8440417B2
申请人:——
公开号:US8440417B2
公开(公告)日:2013-05-14
[EN] METHODS FOR ASSAYING COMPOUNDS OR AGENTS FOR ABILITY TO DISPLACE POTENT LIGANDS OF HEMATOPOIETIC PROSTAGLANDIN D SYNTHASE<br/>[FR] PROCÉDÉS D'ÉVALUATION DE LA CAPACITÉ DE COMPOSÉS OU D'AGENTS À DÉPLACER DE PUISSANTS LIGANDS DE LA PROSTAGLANDINE D SYNTHASE HÉMATOPOÏÉTIQUE
申请人:CAYMAN CHEM CO
公开号:WO2009140364A2
公开(公告)日:2009-11-19
An exemplary embodiment may be directed to a fluorescence polarization assay that screens compounds or agents for their affinity to hematopoietic prostaglandin D synthase (H-PGDS) based on their ability to displace a fluorophore-containing detection analyte bound to an enzyme comprising the primary amino acid sequence of H-PGDS. Another exemplary embodiment utilizes an enzyme having a maltose binding protein amino-acid sequence fused with an N- terminus of the enzyme.
METHOD FOR ASSAYING COMPOUNDS OR AGENTS FOR ABILITY TO DISPLACE POTENT LIGANDS OF HEMATOPOIETIC PROSTAGLANDIN D SYNTHASE
申请人:Maxey Kirk W.
公开号:US20090286261A1
公开(公告)日:2009-11-19
An exemplary embodiment may be directed to a fluorescence polarization assay that screens compounds or agents for their affinity to hematopoietic prostaglandin D synthase (H-PGDS) based on their ability to displace a fluorophore-containing detection analyte bound to an enzyme comprising the primary amino acid sequence of H-PGDS. Another exemplary embodiment utilizes an enzyme having a maltose binding protein amino-acid sequence fused with an N-terminus of the enzyme.