imported>Sarah Richardson |
imported>Sarah Richardson |
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| This section should discuss how the process is used in practice. | | This section should discuss how the process is used in practice. |
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| ==Examples==
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| If you have used a lot of equations in your article, this may be a good place to show an example of how they are used. See the article on the Antoine Equation for an example.
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| {{CZ:Cornell University 2010 BEE 4640 Bioseparation Processes/EZnotice}}
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| {{subpages}}
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| '''Electrophoresis''' is a separation technique frequently used in the analysis of proteins and nucleic acids. The process known as electrophoresis, involves the migration of particles or molecules (in particular proteins, DNA, and RNA) through an electric field that separates them exclusively on the basis of their size or molecular weight. The direction the molecule moves depends on its charge while the rate of migration is affected by the size, shape, density of the gel and the strength of the applied current (5c).
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| Electrophoresis is a very simple process and relatively quick with a high resolution. In addition electrophoresis is an extremely useful method to estimate the purity of a sample. The technique is also very sensitive to slight variations in molecular weight, size, and even shape of nucleic acids and proteins (1). Electrophoresis can also be useful when it doesn’t affect the molecule’s structure or denature the protein (1).
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| ==The Process==
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| Here, go into more detail about the process.
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| ==History==
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| This section should describe the invention and development of the process. If the section runs long, divide it into chronological subsections, for example:
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|
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| ===Invention and early development===
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|
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| This subsection should provide some historical context for the development of your process, describe its invention, and name some early developers and/or applications.
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|
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| ===Recent developments===
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| This section should discuss new developments in the field. Don't hesitate to drop in brief mentions of processes or features you don't intend to discuss in depth. By so doing you are planting seeds of articles which will eventually be developed by others.<ref>"New Directions for Flocculation," American Flocculation Society. 2006. Retrieved July 21, 2009 from [http://www.amflocsoc.org/future_devs.html http://www.amflocsoc.org/future_devs.html]</ref>
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|
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| ==Design and Operation==
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| Use lots of subsections here as you describe various aspects of the process .
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|
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| ==Applications==
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| This section should discuss how the process is used in practice.<ref>"Major Success for Bioprocess Fractionation," ''Anytown Daily News'', January 1, 2015, p. A6.</ref>
| |
|
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| ==Examples==
| |
|
| |
| If you have used a lot of equations in your article, this may be a good place to show an example of how they are used. See the article on the Antoine Equation for an example.
| |
|
| |
| {{CZ:Cornell University 2010 BEE 4640 Bioseparation Processes/EZnotice}}
| |
| {{subpages}}
| |
|
| |
| '''Electrophoresis''' is a separation technique frequently used in the analysis of proteins and nucleic acids. The process known as electrophoresis, involves the migration of particles or molecules (in particular proteins, DNA, and RNA) through an electric field that separates them exclusively on the basis of their size or molecular weight. The direction the molecule moves depends on its charge while the rate of migration is affected by the size, shape, density of the gel and the strength of the applied current (5c).
| |
| Electrophoresis is a very simple process and relatively quick with a high resolution. In addition electrophoresis is an extremely useful method to estimate the purity of a sample. The technique is also very sensitive to slight variations in molecular weight, size, and even shape of nucleic acids and proteins (1). Electrophoresis can also be useful when it doesn’t affect the molecule’s structure or denature the protein (1).
| |
|
| |
| ==The Process==
| |
|
| |
| Here, go into more detail about the process.
| |
|
| |
| ==History==
| |
|
| |
| This section should describe the invention and development of the process. If the section runs long, divide it into chronological subsections, for example:
| |
|
| |
| ===Invention and early development===
| |
|
| |
| This subsection should provide some historical context for the development of your process, describe its invention, and name some early developers and/or applications.<ref>John Q. Sample, ''Chromatography, a new analytical tool''. City: Publisher, 1885.</ref>
| |
|
| |
| ===Recent developments===
| |
|
| |
| This section should discuss new developments in the field. Don't hesitate to drop in brief mentions of processes or features you don't intend to discuss in depth. By so doing you are planting seeds of articles which will eventually be developed by others.<ref>"New Directions for Flocculation," American Flocculation Society. 2006. Retrieved July 21, 2009 from [http://www.amflocsoc.org/future_devs.html http://www.amflocsoc.org/future_devs.html]</ref>
| |
|
| |
| ==Design and Operation==
| |
| Use lots of subsections here as you describe various aspects of the process .<ref>First Author and Second Author, "Electro-absorpto-crossflow-sedimento-extractofractionation," ''Journal of Superspecialized Bioseparation Arcana'' 36:2 (2010) pp. 86-52.</ref>
| |
|
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| ==Applications==
| |
|
| |
| This section should discuss how the process is used in practice.<ref>"Major Success for Bioprocess Fractionation," ''Anytown Daily News'', January 1, 2015, p. A6.</ref>
| |
|
| |
| ==Examples==
| |
|
| |
| If you have used a lot of equations in your article, this may be a good place to show an example of how they are used. See the article on the Antoine Equation for an example.
| |
|
| |
| {{CZ:Cornell University 2010 BEE 4640 Bioseparation Processes/EZnotice}}
| |
| {{subpages}}
| |
|
| |
| '''Electrophoresis''' is a separation technique frequently used in the analysis of proteins and nucleic acids. The process known as electrophoresis, involves the migration of particles or molecules (in particular proteins, DNA, and RNA) through an electric field that separates them exclusively on the basis of their size or molecular weight. The direction the molecule moves depends on its charge while the rate of migration is affected by the size, shape, density of the gel and the strength of the applied current (5c).
| |
| Electrophoresis is a very simple process and relatively quick with a high resolution. In addition electrophoresis is an extremely useful method to estimate the purity of a sample. The technique is also very sensitive to slight variations in molecular weight, size, and even shape of nucleic acids and proteins (1). Electrophoresis can also be useful when it doesn’t affect the molecule’s structure or denature the protein (1).
| |
|
| |
| ==The Process==
| |
|
| |
| Here, go into more detail about the process.
| |
|
| |
| ==History==
| |
|
| |
| This section should describe the invention and development of the process. If the section runs long, divide it into chronological subsections, for example:
| |
|
| |
| ===Invention and early development===
| |
|
| |
| This subsection should provide some historical context for the development of your process, describe its invention, and name some early developers and/or applications.<ref>John Q. Sample, ''Chromatography, a new analytical tool''. City: Publisher, 1885.</ref>
| |
|
| |
| ===Recent developments===
| |
|
| |
| This section should discuss new developments in the field. Don't hesitate to drop in brief mentions of processes or features you don't intend to discuss in depth. By so doing you are planting seeds of articles which will eventually be developed by others.<ref>"New Directions for Flocculation," American Flocculation Society. 2006. Retrieved July 21, 2009 from [http://www.amflocsoc.org/future_devs.html http://www.amflocsoc.org/future_devs.html]</ref>
| |
|
| |
| ==Design and Operation==
| |
| Use lots of subsections here as you describe various aspects of the process .<ref>First Author and Second Author, "Electro-absorpto-crossflow-sedimento-extractofractionation," ''Journal of Superspecialized Bioseparation Arcana'' 36:2 (2010) pp. 86-52.</ref>
| |
|
| |
| ==Applications==
| |
|
| |
| This section should discuss how the process is used in practice.<ref>"Major Success for Bioprocess Fractionation," ''Anytown Daily News'', January 1, 2015, p. A6.</ref>
| |
|
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|
| ==Examples== | | ==Examples== |
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| ==References== | | ==References== |
| <references/> | | <references/> |
| <ref>Harrison, R. G., Todd, P., Rudge S. R., Petrides, D. P. (2003). Bioseparations Science and Engineering. New York, NY: Oxford University Press.</ref>
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| (2) Biochem book
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| Nelson, D. L., Cox, M. M. (2008). Lehninger Principles of Biochemistry (5th ed.). New York, NY: W.H. Freeman and Company.
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| a. Online biochem book
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| http://bcs.whfreeman.com/lehninger5e/
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| (3) Bio lab notes
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| Chen, K., Glase, J. (2009-2010). Chapter 13 – DNA Technology: From Recombination to Genomic Sequencing and Forensic Analysis. In Chen, K. & Hester, L. L. (Eds.), Investigative Biology a laboratory text (pp. 245-288). Plymouth, MI: Hayden McNeil.
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| (4) Bio online textbook
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| Campbell, N. A., Reece, J. B., Urry, L. A., Cain, M. L., Wasserman, S. A., Minorshky, P. V., et al. (2008). Biology (8th ed.). San Francisco, CA: Benjamin Cummings.
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