Abstract: A burn-in socket includes a base, a sliding plate mounted to the base and having a number of pin holes, a number of contacts secured to the base and an actuator mounted on the base. The contacts each comprise a base portion and a pair of arms received in the pin holes of the sliding plate. The actuator includes a frame and a number of actuating portion for driving the sliding plate to move in a transversal direction. The sliding plate includes a number of projections adjacent to contacts. Each projection and the pair of arms of an adjacent contact together define a receiving space and located at three sides of the receiving space, respectively.

Abstract: The application relates to a tool and a method for customizing hint. According to the invention, provided is at least one hint service adapter configured to collect relevant information of different database platforms, validate customized hint on real database platforms and provide feedback, and deploy the customized hint on database platform. Also provided is hint defining means configured to customize hint independently of database platforms, and providing customized hint to the at least one hint service adapter.

Abstract: A low cost single lens array for use in an automatic optical inspection system, so as to reduce parallax, cross talk, and sensitivity to lateral fabrication errors, and a method for stitching together image segments formed by the array. The lens array comprises a plurality of tube-like baffles, within which are disposed single lens sets and linear image sensors. These baffles are typically arranged to provide de-magnified and inverted image segments that are stitched together to provide the entire image of the surface object.

Abstract: The present invention relates to the discovery that serum amyloid A (SAA) is a ligand for the FPRL1 receptor. Disclosed herein, are novel biological tools for the study of SAA/FPRL1 complex assembly and prophylactics, therapeutics, and methods of use of the foregoing, which modulate the association of SAA with FPRL1 and thereby effect responses including, but not limited to, signal transduction, chemotaxis, leukocyte migration, immune system response, amyloidosis, inflammatory response, infection, organ rejection, arthritis, atherosclerosis, and neoplasia.

Abstract: The present invention relates to the discovery that T20/DP178, T21/DP107, and fragments thereof interact with members of the formyl peptide receptor family and thereby modulate cell migration and activation. Novel biological tools, prophylactics, therapeutics and methods of use of the foregoing for modulating an inflammatory response are disclosed.

Abstract: The present invention relates to the discovery that T20/DP178, T21/DP107, and fragments thereof interact with members of the formyl peptide receptor family and thereby modulate cell migration and activation. Novel biological tools, prophylactics, therapeutics and methods of use of the foregoing for modulating an inflammatory response are disclosed.

Abstract: The present invention relates to the discovery that serum amyloid A (SAA) is a ligand for the FPRL1 receptor. Disclosed herein, are novel biological tools for the study of SAA/FPRL1 complex assembly and prophylactics, therapeutics, and methods of use of the foregoing, which modulate the association of SAA with FPRL1 and thereby effect responses including, but not limited to, signal transduction, chemotaxis, leukocyte migration, immune system response, amyloidosis, inflammatory response, infection, organ rejection, arthritis, atherosclerosis, and neoplasia.