Appeal No. 1995-2374 Application 07/673,158 clear that claim 5 refers to the amino acid sequence of Figure 1 while claim 6 refers to the nucleotide sequence of Figure 1. Both rejections under 35 U.S.C. § 112, second paragraph, are reversed. 2. Enablement As explained on pages 3-4 of the Examiner's Answer, the examiner believes that the claims on appeal must be limited to the “nucleic acid sequence of Figure 1.” We disagree. Again, in making this rejection, the examiner has not used the correct legal standard. The issue raised by the examiner is whether one skilled in the art could make and use the claimed invention throughout its scope without undue experimentation. As set forth in the sentence bridging pages 3-4 of the Examiner's Answer: “It would require undue experimentation for one of skill in the art to have to make every protein which has 'at least 80% homology' with the protein whose sequence is given in Figure 1 and then to test every single one of these homologues to determine whether it will function to 'fold [newly synthesized proteins] into their biologically active conformation.” As explained in PPG Indus., Inc. v. Guardian Indus. Corp., 75 F.3d 1558, 1564, 37 USPQ2d 1618, 1623 (Fed. Cir. 1996): In unpredictable art areas, this court has refused to find broad generic claims enabled by specifications that demonstrate the enablement of only one or a few embodiments and do not demonstrate with reasonable specificity how to make and use other potential embodiments across the full scope of the claim. See, e.g., In re Goodman, 11 F.3d 1046, 1050-52, 29 USPQ2d 2010, 2013-15 (Fed. Cir. 1993); Amgen, Inc. v. Chugai Pharmaceutical Co., 927 F.2d 1200, 1212-14, 18 USPQ2d 1016, 1026-28 (Fed. Cir.), cert. denied, 502 U.S. 856 (1991); In re Vaeck, 947 F.2d at 496, 20 USPQ2d at 4Page: Previous 1 2 3 4 5 6 7 8 NextLast modified: November 3, 2007