Appeal No. 2001-1293 Page 13 Application No. 08/464,271 conclusion of nonenablement. As we discussed above, the remaining grounds set out by the examiner are inadequate to support the rejection. Therefore, the examiner has not shown that claims 40 and 41 are not enabled for a method of making transgenic organisms. In addition to the “transgenic animals” analysis discussed in detail above, the examiner set out a second enablement analysis, based on the disclosed use of the claimed system in gene therapy. We do not agree that any potential problems that might be encountered using the claimed system in gene therapy support a rejection for nonenablement. The specification discloses that the claimed method can be used to “create valuable animal models.” Page 19. There is no rejection for lack of utility before us, and the examiner has conceded that the claims are enabled with respect to mice lacking lymphoid cells. See the Examiner’s Answer, page 4. Thus, the examiner does not appear to dispute that tissue-specific cell ablation would be useful in making animal models for research. “The enablement requirement is met if the description enables any mode of making and using the invention.” Johns Hopkins Univ. v. CellPro Inc., 152 F.3d 1342, 1361, 47 USPQ2d 1705, 1714 (Fed. Cir. 1998) (quoting Engel Indus., Inc. v. Lockformer Co., 946 F.2d 1528, 1533, 20 USPQ2d 1300, 1304 (Fed. Cir. 1991)). Since the specification describes one method of making and using the invention of claims 40 and 41, it enables these claims, whether or not the claimed method is also enabled for use in gene therapy. Therefore, we reverse the examiner’s rejection with respect to claims 40 and 41.Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 NextLast modified: November 3, 2007