Ex parte PETTERSSON et al. - Page 6


              Appeal No.  2001-1412                                                        Paper No. 29                
              Application No.  08/629,177                                                  Page 6                      


                     because Rutner et al. specifically disclose that the solid substrate containing                   
                     the labeled form of the ligand and receptor are aspirated and dried in vacuo                      
                     prior to use in the assay (column 4, lines 27-31) to provide for a one-step                       
                     assay.  One of ordinary skill in the art would have been motivated to dry all of                  
                     the assay reagents in the assays taught by Deeg et al. and use fluorescent                        
                     markers on the labelled binding partner because doing so would allow for a                        
                     one-step efficient assay that could be used to detect large numbers of                            
                     samples and the dried reagents would preserve better.  The use of                                 
                     fluorescent markers in Deeg would eliminate the need for the addition of any                      
                     reagents after the wash step.  [Answer, pp. 5-6.]                                                 
                     First, the examiner has not pointed out, and we do not find, where Deeg discloses                 
              or suggests using a reaction/test well as a suitable substrate for applying reagents using               
              an ink-jet printer.  The examiner has not stated what she considers to be the reaction wells             
              in Deeg or where appellants’ specification defines “reaction well” as anything other than a              
              conventional well, e.g., a well in a microtitration plate or a microtitration strip, as shown in         
              appellants’ Figs. 1A and 1B (see also specification, p. 3, l. 21; p. 5, ll. 12-13; p. 13, l. 12; p.      
              14, l. 17).  Furthermore, although Rutner describes solid phase substrates as being “in                  
              particulate form, sheet form or in the form of a test tube” (c. 2, ll. 41-42), Deeg only                 
              describes “printing” reagents on one form, i.e., a sheet or “film” of plastic, using an ink-jet          
              printer.  The examiner has not established that it would have been within ordinary skill in              
              the art to modify an ink-jet printer to “print” reagents inside a test tube or reaction well             
              instead of on a carrier film or sheet.                                                                   
                     Second, Deeg describes multiple discrete rows of each reagent not single layers of                
              each reagent (brief, pp. 11-12), i.e., not an “analyte specific component [immobilized] ... in           
              a single continuous region of said reaction well” as claimed.  The examiner argues that                  
              “Deeg alternates reagent materials for the advantage of faster mix times upon                            







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