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1

Walls, Dermot, and Sinéad T. Loughran, eds. Protein Chromatography. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6412-3.

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2

Walls, Dermot, and Sinéad T. Loughran, eds. Protein Chromatography. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-60761-913-0.

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3

Kenney, Andrew, and Susan Fowell. Practical Protein Chromatography. New Jersey: Humana Press, 1992. http://dx.doi.org/10.1385/0896032132.

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4

Protein chromatography: Methods and protocols. New York, N.Y: Humana Press, 2011.

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5

Carta, Giorgio. Protein chromatography: Process development and scale-up. Weinheim: Wiley-VCH, 2010.

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6

Protein affinity tags: Methods and protocols. New York: Humana Press, 2014.

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7

Lan, Chi-Wei. Protein purification using fluidised bed chromatography: Physical and biochemical characterisation of a simple absorbent contactor. Birmingham: University of Birmingham, 2000.

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8

1945-, Nakanishi Kazuhiro, and Matsuno Ryūichi 1939-, eds. Ion-exchange chromatography of proteins. New York: M. Dekker, 1988.

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9

Staby, Arne, Anurag S. Rathore, and Satinder Ahuja, eds. Preparative Chromatography for Separation of Proteins. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119031116.

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10

P, Georgiev G., ed. Khromatografii͡a︡ belkov i nukleinovykh kislot. Moskva: Izd-vo "Nauka", 1985.

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11

International, Symposium on High-performance Liquid Chromatography of Proteins Peptides and Polynucleotides (7th 1987 Washington D. C. ). Seventh International Symposium on High-performance Liquid Chromatography of Proteins, Peptides and Polynucleotides, Washington, D. C., November 2-4, 1987. Amsterdam: Elsevier, 1988.

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12

Podzimek, Stepan. Light scattering, size exclusion chromatography, and asymmetric flow field flow fractionation: Powerful tools for the characterization of polymers, proteins and nanoparticles. Hoboken, N.J: Wiley, 2011.

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13

Andrew, Kenney, and Fowell Susan, eds. Practical protein chromatography. Totowa, N.J: Humana Press, 1992.

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14

1946-, Kastner Michael, ed. Protein liquid chromatography. Amsterdam: Elsevier, 2000.

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15

Protein Liquid Chromatography. Elsevier, 2000. http://dx.doi.org/10.1016/s0301-4770(08)x6027-0.

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16

(Editor), Jan-Christer Janson, and Lars Ryden (Editor), eds. Protein Purification. Wiley-VCH, 1989.

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17

Kastner, M. Protein Liquid Chromatography (Journal of Chromatography Library). Elsevier Science, 1999.

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18

Kastner. Protein Liquid Chromatography (Journal of Chromatography Library). Elsevier Science, 1999.

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19

Carta, Giorgio, and Alois Jungbauer. Protein Chromatography: Process Development and Scale-Up. Wiley & Sons, Incorporated, John, 2020.

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20

Protein Chromatography: Process Development and Scale-Up. Wiley & Sons, Limited, John, 2010.

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21

Carta, Giorgio, and Alois Jungbauer. Protein Chromatography: Process Development and Scale-Up. Wiley & Sons, Limited, John, 2020.

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22

Carta, Giorgio, and Alois Jungbauer. Protein Chromatography: Process Development and Scale-Up. Wiley & Sons, Incorporated, John, 2020.

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23

Protein Purification: Principles, High Resolution Methods, and Applications (Methods of Biochemical Analysis). 3rd ed. Wiley-VCH, 2008.

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24

Banks, Robert C. Oligodeoxynucleotide affinity column for the isolation of sequence specific DNA binding proteins. 1989.

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25

Roe, Simon, ed. Protein Purification Techniques. Oxford University Press, 2001. http://dx.doi.org/10.1093/oso/9780199636747.001.0001.

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Proteins are an integral part of molecular and cellular structure and function and are probably the most purified type of biological molecule. In order to elucidate the structure and function of any protein it is first necessary to purify it. Protein purification techniques have evolved over the past ten years with improvements in equipment control, automation, and separation materials, and the introduction of new techniques such as affinity membranes and expanded beds. These developments have reduced the workload involved in protein purification, but there is still a need to consider how unit operations linked together to form a purification strategy, which can be scaled up if necessary. The two Practical Approach books on protein purification have therefore been thoroughly updated and rewritten where necessary. The core of both books is the provision of detailed practical guidelines aimed particularly at laboratory scale purification. Information on scale-up considerations is given where appropriate. The books are not comprehensive but do cover the major laboratory techniques and common sources of protein. Protein Purification Techniques focuses on unit operations and analytical techniques. It starts with an overview of purification strategy and then covers initial extraction and clarification techniques. The rest of the book concentrates on different purification methods with the emphasis being on chromatography. The final chapter considers general scale-up considerations. Protein Purification Applications describes purification strategies from common sources: mammalian cell culture, microbial cell culture, milk, animal tissue, and plant tissue. It also includes chapters on purification of inclusion bodies, fusion proteins, and purification for crystallography. A purification strategy that can produce a highly pure single protein from a crude mixture of proteins, carbohydrates, lipids, and cell debris to is a work of art to be admired. These books (available individually or as a set)are designed to give the laboratory worker the information needed to undertake the challenge of designing such a strategy.
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26

Marko-Varga, Gyorgy, and Peter Oroszlan. Emerging Technologies in Protein and Genomic Material Analysis (Journal of Chromatography Library). Elsevier Science, 2003.

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27

György, Marko-Varga, and Oroszlan Peter, eds. Emerging technologies in protein and genomic material anaylsis. Amsterdam: Elsevier, 2003.

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28

J, Simpson Richard, Adams Peter D, and Golemis Erica, eds. Basic methods in protein purification and analysis: A laboratory manual. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory Press, 2008.

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29

Yamamoto, Shuichi. Ion Exchange Chromatography of Proteins, 2nd Edition (Chromatographic Science). 2nd ed. CRC, 2015.

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30

Lattman, Eaton E., Thomas D. Grant, and Edward H. Snell. Distinct Instrumental Approaches to SAXS. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199670871.003.0010.

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There are more specialized applications of SAXS and SANS which require specific experimental considerations. This chapter covers size exclusion chromatography which has proven to be useful to study both soluble and membrane bound proteins allowing the study of samples that show time and concentration dependent dynamics. It also describes iime-resolved techniques for SAXS and in a few cases, SANS. Finally, with improved X-ray sources, detectors, sample handling, and compute power, the ability to perform SAXS data in high-throughput is available. This is discussed in enabling the use of SAXS to study protein interactions, map macromolecular conformation, and rapidly characterize samples amongst other applications.
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31

1958-, McMahon Robert Joseph, ed. Avidin-biotin interactions: Methods and applications. Totowa, NJ: Humana, 2008.

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32

1958-, McMahon Robert Joseph, ed. Avidin-biotin interactions: Methods and applications. Totowa, NJ: Humana, 2008.

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33

Avidin-Biotin Interactions: Methods and Applications (Methods in Molecular Biology). Humana Press, 2008.

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34

Matejtschuk, Paul. Affinity Separations: A Practical Approach (Practical Approach Series). Oxford University Press, USA, 1997.

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35

Matejtschuk, Paul. Affinity Separations: A Practical Approach (Practical Approach Series). Oxford University Press, USA, 1997.

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36

Paul, Matejtschuk, ed. Affinity separations: A practical approach. Oxford: Oxford University Press, 1997.

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37

Sofer, G. K. Process Chromatography: A Practical Guide. Academic Press, 1989.

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38

Analytical Techniques for Biopharmaceutical Development. CRC, 2005.

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39

Paul, Millner, ed. High resolution chromatography: A practical approach. Oxford: Oxford University Press, 1999.

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40

(Editor), Robert A. Boudreau, and Sharon M. Boudreau (Editor), eds. Passive Micro-Optical Alignment Methods (Optical Engineering). CRC, 2005.

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41

Rathore, Anurag S., Satinder Ahuja, and Arne Staby. Preparative Chromatography for Separation of Proteins. Wiley & Sons Canada, Limited, John, 2017.

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42

Rathore, Anurag S., Satinder Ahuja, and Arne Staby. Preparative Chromatography for Separation of Proteins. Wiley & Sons, Incorporated, John, 2017.

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43

Rathore, Anurag S., Satinder Ahuja, and Arne Staby. Preparative Chromatography for Separation of Proteins. Wiley & Sons, Incorporated, John, 2017.

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44

Liquid Chromatography: Applications. Elsevier Science & Technology Books, 2017.

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45

Liquid Chromatography: Applications. Elsevier Science & Technology Books, 2013.

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46

High-Performance Liquid Chromatography of Peptides and Proteins. CRC Press, 2017. http://dx.doi.org/10.1201/9780203751947.

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47

A, Vijayalakshmi M., ed. Biochromatography: Theory and practice. London: Taylor & Francis, 2002.

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48

Liquid Chromatography: Fundamentals and Instrumentation. Elsevier Science & Technology Books, 2017.

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49

Liquid Chromatography: Fundamentals and Instrumentation. Elsevier Science & Technology Books, 2013.

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50

E, Kruger James, and Bietz Jerold A, eds. High-performance liquid chromatography of cereal and legume proteins. St. Paul, Minnesota: American Association of Cereal Chemists, Inc., 1994.

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