Raymond C. Milton
Beckman Coulter
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Featured researches published by Raymond C. Milton.
Methods of Molecular Biology | 2007
Robert S. Matson; Raymond C. Milton; Michael C. Cress; Tom S. Chan; Jang B. Rampal
Here, we provide methods for the creation of protein microarrays in microplates. The microplate consists of 96 wells with each well capable of holding a protein microarray at a spot density of up to 400 (20 x 20) individual elements. Arrays of capture monoclonal antibodies, corresponding to specific interleukins, were printed onto the bottom of the wells which had been surface activated for covalent attachment. A Biomek 2000 laboratory automation workstation (Beckman Coulter, Inc., Fullerton, CA) equipped with a high-density replicating tool was used for printing low density 3 x 3 to 5 x 5 arrays. For higher density arrays, a microarrayer system (Cartesian PS7200, Genomic Solutions, Inc., Ann Arbor, MI) was employed. Multiple antigens were simultaneously analyzed without detectable cross-reactivity associated with capture antibody or secondary antibody interactions. Detection of interleukin antigens, spiked into cell culture media containing 10% fetal calf serum, was specific and sensitive.
Methods of Molecular Biology | 2007
Robert S. Matson; Raymond C. Milton; Jang B. Rampal; Tom S. Chan; Michael C. Cress
The ability to perform microarray-based immunoassays without the need for wells or other fluid barriers were demonstrated. Both contact and noncontact microarray printing technology is used to prepare spotted arrays of analyte binding sites, as well as, to deliver samples, secondary antibodies and other signal development reagents directly to these sites in a parallel fashion are called as overprint immunoassays. A micro-ELISA is demonstrated based upon the use of Protein A as a universal microarray. All components of the assay (capture antibody, antigen, and signal development reagents) were site-specifically dispensed in parallel fashion to the surface in nanoliter volumes. This represents a 1000-fold reduction in reagent consumption from that used in a conventional 96-well microtiter plate assay. Overprinting nanoliter volumes directly onto 200-300 microm spots yields similar levels of sensitivity achieved with the bulk dispensing of microliter volumes into wells.
Archive | 2000
Robert S. Matson; Raymond C. Milton
Archive | 2000
Raymond C. Milton
Archive | 2005
Robert S. Matson; Raymond C. Milton; Robert J. Obremski; John W. Silzel
Archive | 1999
Raymond C. Milton
Archive | 2005
Robert S. Matson; Raymond C. Milton
Archive | 2002
Raymond C. Milton
Archive | 2003
Robert S. Matson; Raymond C. Milton; Robert J. Obremski; John W. Silzel
Archive | 2000
Robert S. Matson; Raymond C. Milton