Based on systematic analysis, an Integrated Plant Maintenance System (IPMS)is proposed in this paper to cope with challenges in plant maintenance. The characteristics of theIPMS are summarized and the necessity of its...Based on systematic analysis, an Integrated Plant Maintenance System (IPMS)is proposed in this paper to cope with challenges in plant maintenance. The characteristics of theIPMS are summarized and the necessity of its modeling is set forth. Based on the analysis andcomparison among structured, object-oriented and multi-agent modeling frameworks, a multi-agentmodeling framework is selected in this paper as a theoretical guidance and together with the Troposmethod for modeling, the system model of an integrated plant maintenance system is constructed. Thesystem model developed in this paper provides a guidance template for the Baling company in itsstepwise implementation of the IPMS.展开更多
Bovine fetal oviduct epithelial cells were transfected with constructed double marker selective vector(pCE-EGFP-IRES-Neo-dNdB) containing the enhanced green fluorescent protein (EGFP) and neomycin-resistant(Neo^r) gen...Bovine fetal oviduct epithelial cells were transfected with constructed double marker selective vector(pCE-EGFP-IRES-Neo-dNdB) containing the enhanced green fluorescent protein (EGFP) and neomycin-resistant(Neo^r) genes by electroporation, and a transgenic cell line was obtained. Somatic cell nuclear transfer (SCNT) was cartied out using the transgenic cells as nuclei donor. A total of 424 SCNT embryos were reconstructed and 208 (49.1%) of them developed to blastocyst stage. 17 blastocysts on D 7 after reconstruction were transferred to 17 surrogate calves,and 5 (29.4%) recipients were found to be pregnant. Three of them maintained to term and delivered three cloned calves.PCR and Southern blot analysis confirmed the integration of transgene in all of the three cloned calves. In addition, expression of EGFP was detected in biopsy isolated from the transgenic cloned calves and fibroblasts derived from the biopsy. Our results suggest that transgenic calves could be efficiently produced by SCNT using transgenic cells as nuclei donor. Furthermore, all cloned animals could be ensured to be transgenic by efficiently pre-screening transgenic cells and SCNT embryos using the constructed double marker selective vector.展开更多
基金theHunanProvince(China)DemonstrationProgramforInformatizationinManufactureun derGrantNo. Hnmie A 070,andHunanProvinceScienceandTechnologyDepartmentPlanProjectunderGrantNo.03GKY3057
文摘Based on systematic analysis, an Integrated Plant Maintenance System (IPMS)is proposed in this paper to cope with challenges in plant maintenance. The characteristics of theIPMS are summarized and the necessity of its modeling is set forth. Based on the analysis andcomparison among structured, object-oriented and multi-agent modeling frameworks, a multi-agentmodeling framework is selected in this paper as a theoretical guidance and together with the Troposmethod for modeling, the system model of an integrated plant maintenance system is constructed. Thesystem model developed in this paper provides a guidance template for the Baling company in itsstepwise implementation of the IPMS.
文摘Bovine fetal oviduct epithelial cells were transfected with constructed double marker selective vector(pCE-EGFP-IRES-Neo-dNdB) containing the enhanced green fluorescent protein (EGFP) and neomycin-resistant(Neo^r) genes by electroporation, and a transgenic cell line was obtained. Somatic cell nuclear transfer (SCNT) was cartied out using the transgenic cells as nuclei donor. A total of 424 SCNT embryos were reconstructed and 208 (49.1%) of them developed to blastocyst stage. 17 blastocysts on D 7 after reconstruction were transferred to 17 surrogate calves,and 5 (29.4%) recipients were found to be pregnant. Three of them maintained to term and delivered three cloned calves.PCR and Southern blot analysis confirmed the integration of transgene in all of the three cloned calves. In addition, expression of EGFP was detected in biopsy isolated from the transgenic cloned calves and fibroblasts derived from the biopsy. Our results suggest that transgenic calves could be efficiently produced by SCNT using transgenic cells as nuclei donor. Furthermore, all cloned animals could be ensured to be transgenic by efficiently pre-screening transgenic cells and SCNT embryos using the constructed double marker selective vector.
