Ex Parte CASTRO - Page 4



              Appeal No. 2003-0892                                                                  Page 4                
              Application No. 09/454,385                                                                                  
              “[T]arget DNA of unknown sequence is labeled with a fluorophore and combined with                           
              transponder particles carrying known oligonucleotides . . . [t]he transponders are                          
              analyzed to detect the fluorescence or color originating from a label that indicates that                   
              target DNA has bound to the probe attached to the . . . transponder, and the                                
              information stored electronically in the transponder is decoded” (column 1, lines 49-68).                   
              As appellant points out, “each transponder has a surface that is covered with the                           
              encoded oligonucleotides . . . so that a large fluorescent signal is obtained from the                      
              multitude of labeled target sequences rather than extended reporter molecules on each                       
              target sequence” (Brief, page 3).  As the examiner puts it, Mandecki “detect[s] the                         
              fluorescence emitted by each and every fluorophore of each and every individual                             
              reporter molecule . . . at the same time and joins them together” (Answer, page 7).                         
                     Albrecht describes a method for identifying and isolating differentially expressed                   
              genes or polymorphic genes.  “[D]ifferently labeled populations of DNAs from cell or                        
              tissue sources whose gene expression is to be compared [are provided and] . . .                             
              competitively hybridized with reference DNA cloned on solid phase supports” (column                         
              2, lines 28-48).  The reference oligonucleotides “are synthesized on the surface of a                       
              solid phase support, such as a microscopic bead or a specific location on an array of                       
              synthesis locations on a single support, such that populations of identical . . .                           
              sequences are produced in specific regions.  That is, the surface of each support, in the                   
              case of a bead, or of each region, in the case of an array, is derivatized by copies of                     
              only one type of tag complement having a particular sequence” (column 10, lines 18-                         
              29).  Appellant argues that Albrecht thus “fail[s] to teach [appellant’s] recited method                    
              steps for identifying single target molecules or for extending a primer molecule along                      
              the single target sequences so that individual target sequences can be identified                           




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