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Protein Chromatography

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Cover of 'Protein Chromatography'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 A Synopsis of Proteins and Their Purification
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    Chapter 2 Mixed-Mode Chromatography and Its Role in Monoclonal Antibody Purification
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    Chapter 3 Continuous Countercurrent Chromatography in Protein Purification
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    Chapter 4 Chromatographic Purification of Viral Vectors for Gene Therapy Applications
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    Chapter 5 Scale-Up of Protein Purification: Downstream Processing Issues
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    Chapter 6 Approaches to Avoid Proteolysis During Protein Expression and Purification
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    Chapter 7 Tagging Recombinant Proteins to Enhance Solubility and Aid Purification
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    Chapter 8 Magnetic Nanoparticles for Protein Separation and Purification.
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    Chapter 9 Ion-Exchange Chromatography: Basic Principles and Application
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    Chapter 10 Hydroxyapatite Chromatography (HAC).
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    Chapter 11 Poly-Histidine-Tagged Protein Purification Using Immobilized Metal Affinity Chromatography (IMAC)
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    Chapter 12 Lectin Affinity Chromatography
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    Chapter 13 Single-Step Non-Chromatographic Purification of Recombinant Mammalian Proteins Using a Split Intein ELP Tag System
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    Chapter 14 Clinical Proteomics: Liquid Chromatography-Mass Spectrometry (LC-MS) Purification Systems
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    Chapter 15 Immunoprecipitation Immunoprecipitation (IP) : Variations, Considerations, and Applications
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    Chapter 16 Protein Quantitation and Analysis of Purity
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    Chapter 17 Protein Extraction and Purification by Differential Solubilization
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    Chapter 18 Protein Stability: Enhancement and Measurement
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    Chapter 19 Storage and Lyophilization of Pure Proteins
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    Chapter 20 Strategies for the Purification of Membrane Proteins.
Attention for Chapter 10: Hydroxyapatite Chromatography (HAC).
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Chapter title
Hydroxyapatite Chromatography (HAC).
Chapter number 10
Book title
Protein Chromatography
Published in
Methods in molecular biology, January 2023
DOI 10.1007/978-1-0716-3362-5_10
Pubmed ID
Book ISBNs
978-1-07-163361-8, 978-1-07-163362-5
Authors

Cawley, Jonathan

Abstract

Hydroxyapatite (HA) is a mixed-mode media that has been used extensively for the purification of proteins and DNA since the 1950s. Hydroxyapatite possesses a distinctive selectivity that may be applied in the purification of a wide range of biomolecules: immunoglobulins, alkaline proteins, acidic proteins, and DNA. The functional groups of HA can both attract and repel the carboxyl and amino groups on target molecules. This unique selectivity is due to the modalities that can be employed, which are not possible with traditional anion-exchange and cation-exchange chromatography. HA is a powerful chromatography step for reducing host cell-derived impurities and aggregated product, where a 2-4 log reduction in host cell proteins, aggregates, endotoxin, and viruses are routinely achieved. This chapter describes the procedures for: efficiently packing and evaluating a HA column, purifying IgG and acidic proteins respectively using HA chromatography.

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Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 30 August 2023.
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#17,283,047
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#5,987
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Outputs of similar age from Methods in molecular biology
#286
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