| US 7,531,316 B2 | ||
| High throughput assay of Lp-PLA2 activity | ||
| Yun-Fu Hu, Research Triangle Park, N.C. (US); and George T. Walker, Research Triangle Park, N.C. (US) | ||
| Assigned to Glaxo Group Limited, Greenford, Middlesex (United Kingdom) | ||
| Appl. No. 10/557,540 PCT Filed May 27, 2004, PCT No. PCT/US2004/016716 § 371(c)(1), (2), (4) Date Nov. 21, 2005, PCT Pub. No. WO2005/001416, PCT Pub. Date Jan. 06, 2005. |
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| Claims priority of provisional application 60/473777, filed on May 28, 2003. | ||
| Prior Publication US 2007/0065892 A1, Mar. 22, 2007 | ||
| Int. Cl. C12Q 1/34 (2006.01) | ||
| U.S. Cl. 435—18 [435/198] | 53 Claims |
| 1. A method for determining an Lp-PLA2 enzyme activity in a plurality of samples comprising the steps of preparing a solution comprising labeled PAF; contacting each of a plurality of tissue samples with the solution of the preparing step and with a sequester molecule of PAF, wherein said sequester molecule is exogenous BSA, to form a PAF-sequester molecule complex; removing said PAF-sequester molecule complex; and detecting an Lp-PLA2 activity by measuring the amount of PAF cleaved by said Lp-PLA2 enzyme wherein said amount of cleaved PAF determines Lp-PLA2 activity. |