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Laboratory Methods |
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Overview Microscope studies Flagella experiment Laboratory math Blood fractionation Gel electrophoresis Protein gel analysis Mitochondria Concepts/ theory |
Overview Keeping a lab notebook Writing research papers Dimensions & units Using figures (graphs) Examples of graphs Experimental error Representing error Applying statistics |
Overview Principles of microscopy Solutions & dilutions Protein assays Spectrophotometry Fractionation & centrifugation Radioisotopes and detection |
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Selected Laboratory MethodsThis section deals with instrumentation and methodology that is applicable to a variety of laboratory studies. The information here might serve as a suitable reference for future laboratory work. MicroscopyPresented are principles of bright field, oil immersion, dark field, phase contrast, and D.I.C. optics and recommended specimens on which to practice. Methods for measurement with a light microscope are described, including use of a cell counting chamber (hemacytometer) and eyepiece reticule. Solutions & dilutionsThis section distinguishes among types of mixtures and defines the term solution. It describes units and prefixes for volume, amount, and concentration, and presents types of formulas that are used to describe solutions. Examples of how to make solutions are presented. This section also describes how to dilute a solution to final desired concentration or to final concentration and volume, again with examples. Protein assaysA general approach to setting up and interpreting a colorimetric assay is presented here. The principles are not limited to protein assays, however the remainder of this section describes assays for protein that have been employed in the past, some of which are still in common use.Spectrophotometry & Beer's LawThis section is brief (one page only), but it is important. It includes a procedure for calibrating a relatively simple spectrophotometer, the Spectronic 20. Fractionation/centrifugationHere you will find a general scheme for "taking apart" cells and tissues, and separating components by a process called differential centrifugation. It includes the concepts of fractions and yields, describes some limitations on reporting yields, and describes how information related to fractionation is typically presented in a paper. |
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and Intended Use Visitors: to ensure that your message is not mistaken for SPAM, please include the acronym "Bios211" in the subject line of e-mail communications Created by David R. Caprette (caprette@rice.edu), Rice University 10 Aug 12 |