Appeal 2007-0725 Reexamination Control 90/006,785 Patent 5,073,484 14. Patentee also directs us to portions of Cleeland and Murachi. (Br. at 13). 15. Cleeland states that “[e]xisting procedures for fluorescent labeling of protein, for example, labeling with fluorescein isothiocyanate (FITC) rely upon fluorophors with reactive functionalities which will covalently bind to proteins.” (Cleeland at 1:13-17). 16. Murachi states that “in using an enzyme protein as a label it is desirable that the enzyme molecule be bound firmly by a covalent bond to an antigen or antibody that is to be assayed.” (Murachi at 1). Deutsch 17. Deutsch discloses “test devices and methods for their use in performing binding assays such as for determining a ligand in … a sample of a biological fluid.” (Deutsch at 1:7-14). 18. In Deutsch a sample to be tested is dispensed on a sample receiving portion of a strip. (Deutsch at 3:58-61). 19. The strip is then immersed in “developing fluid” which advances along the strip. (Deutsch at 3:59-62). 20. When the developing fluid meets the sample, the two are combined and the developing fluid carries the sample forward. (Deutsch at 3:63-64). 21. At a point thereafter on the strip, the sample is exposed to a reagent for the material to be detected. (Deutsch at 3:65-4:3). 22. If sample is present, a detectable response occurs. (Deutsch at 4:3-5). 23. The reagent for the material to be detected may be labeled with “any chemical substance or moiety having a detectable characteristic which is 7Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Next
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