Course Objectives: [return to top]
1) Read and follow instructions for laboratory procedures as described in Standard Operating Procedures (SOPs) and other written documents.
2) Maintain written records of laboratory work, including maintaining a lab notebook documenting lab procedures, calculations, measurements, observations, and analysis of results
3) Safely, efficiently and effectively prepare chemical solutions, including the performance of calculations necessary to the preparation of solutions described by molarity, weight per volume and percentage.
4) Calibrate and use a variety of basic laboratory equipment to include pipettors, balances, pH meters, autoclaves.
5) Demonstrate understanding of the principles of aseptic technique and how they apply to the manipulation and maintenance of both bacterial and eukaryotic cell cultures.
6) Recognize, and be able to appropriately manipulate and quantify, bacterial cultures of E. coli, various common bacteriophage, and eukaryotic (mammalian) cell cultures, using terms such as titer, generation time, and confluency.
7) Explain the process of using assays to determine unknown quantities, demonstrate an understanding of the underlying principles of visible and UV spectroscopy in this task, and be able to accurately perform both endpoint and kinetic rate assays, demonstrating understanding of the principles of range, limitations, linearity, interference and reproducibility in the collection and analysis of valid data.
8) Demonstrate understanding of the principles of electrophoresis as they relate to the separation of various biomolecules by their physical properties and be able to prepare a variety of gels and use them effectively to separate these molecules.
9) Apply basic knowledge of a biomolecule’s properties, such as cellular localization, size, charge, and function to achieve purification of the molecule from complex mixtures using column chromatography and calculate yield, specific activity and fold-purification.
10) Accurately follow procedures to isolate DNA from biological sources, assess the yield and integrity of the product, introduce the foreign DNA into cultured cells, and perform protocols (ELISA/Western) using antibody reagents to detect the presence and quantity of specific proteins produced as the result of the inserted DNA. |
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