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- 자연과학 >생물ㆍ화학ㆍ환경 >생명공학
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- 강의학기
- 2017년 1학기
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- 강의계획서
- 강의계획서
유전공학은 현대 생명공학에 가장 많이 이용되어지고 있는 생명공학기법중에 하나로써 유전자 시퀀싱과 재조합 기술을 이용하여 DNA를 조작하여 생물체에 새로운 형질을 부여하거나 기존의 형질을 향상시키는 응용학문이다. 본 과목에서는 이러한 유전공학적 기술에 필요한 기본적인 지식을 습득하고 이를 바탕으로 기존의 예를 통하여 유전공학기술을 이용하여 새로운 의약품 또는 의약품의 대량생산에 활용할 수 있는 능력을 배양하는 것을 목표로 한다.
- 수강안내 및 수강신청
- ※ 수강확인증 발급을 위해서는 수강신청이 필요합니다
차시별 강의
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Molecular biotechnology | Recombinant DNA technology, Commercialization of molecular biotechnology products, Concerns | |
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Recombinant DNA technology | Restriction endonucleases, Ligation | |
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Plasmid cloning vectors | Plasmid cloning vectors, Plasmid cloning vector pBR322, Other plasmid cloning vectors | |
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Plasmid cloning vectors | Cosmids, Types of cloning vectors | |
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Creating and screening a library | Making a genomic library, Screening by DNA hybridization / immunological assay / protein activity | |
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Creating and screening a library | Cloning DNA sequences that encode eukaryotic proteins | |
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Chemical synthesis of DNA | Chemical synthesis of DNA | |
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Chemical synthesis of DNA | Uses of synthesized oligonucleatides | |
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Polymerase Chain Reaction | Polymerase Chain Reaction | |
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DNA sequencing techniques | DNA sequencing techniques | |
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Sequencing and imaging | Cyclic reversible termination | |
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Sequencing and imaging | Sequencing by ligation, Pyrosequencing | |
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Sequencing and imaging, Functional genomics | Real-time sequencing, GenBank sequence depository | |
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Functional genomics | Functional genomics, DNA microarray | |
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Functional genomics | Senal analysis of gene expression(SAGE) | |
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Proteomics | Protein expression profiling: 2D differential in-gel electrophoresis & ICAT, Protein microarrays | |
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Manipulation of gene expression | Basic features of gene expression control, Promoter control | |
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Manipulation of gene expressionFusion Proteins | regulatable promoters, pCP3 expression system, Sigma factor | |
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Fusion proteins | Use of fusion protein, Cleavage of fusion protein | |
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other factors attecting gene expression | Increasing protein stability, Increasing secretion, Metabolic load | |
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Directed mutagenesis | Oligonucleotide-directed mutagenesis with plasmid, PCR amplified oligonucieotide directed mutagenesis | |
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Examples of protein engineering | protein engineering introduction, Adding disulfide bonds, Increasing enzymatic activity, Decreasing protease sensitivity, Increasing enzyme stability and specificity | |
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