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Vaccine Technologies for Veterinary Viral Diseases

Overview of attention for book
Vaccine Technologies for Veterinary Viral Diseases
Humana Press, New York, NY

Table of Contents

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    Book Overview
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    Chapter 1 Vaccines and Vaccination for Veterinary Viral Diseases: A General Overview.
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    Chapter 2 Using IC-Tagging Methodology for Production and Purification of Epitope-Loaded Protein Microspheres for Vaccination
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    Chapter 3 Plant-Based Vaccine Antigen Production
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    Chapter 4 DNA Vaccines: Experiences in the Swine Model
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    Chapter 5 Novel Adjuvants and Immunomodulators for Veterinary Vaccines.
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    Chapter 6 Polymerase Mechanism-Based Method of Viral Attenuation
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    Chapter 7 Vaccine Technologies for Veterinary Viral Diseases
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    Chapter 8 Laboratory-Scale Production of Replication-Deficient Adenovirus Vectored Vaccines
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    Chapter 9 Generation of Recombinant Modified Vaccinia Virus Ankara Encoding VP2, NS1, and VP7 Proteins of Bluetongue Virus
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    Chapter 10 Generation of Recombinant Capripoxvirus Vectors for Vaccines and Gene Knockout Function Studies
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    Chapter 11 Recombinant Swinepox Virus for Veterinary Vaccine Development
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    Chapter 12 Generation and Selection of Orf Virus (ORFV) Recombinants
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    Chapter 13 Polycistronic Herpesvirus Amplicon Vectors for Veterinary Vaccine Development
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    Chapter 14 Construction and Application of Newcastle Disease Virus-Based Vector Vaccines
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    Chapter 15 Chimeric Pestivirus Experimental Vaccines
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    Chapter 16 Vaccine Technologies for Veterinary Viral Diseases
Attention for Chapter 3: Plant-Based Vaccine Antigen Production
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Chapter title
Plant-Based Vaccine Antigen Production
Chapter number 3
Book title
Vaccine Technologies for Veterinary Viral Diseases
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3008-1_3
Pubmed ID
Book ISBNs
978-1-4939-3007-4, 978-1-4939-3008-1
Authors

Hoang Trong Phan, Udo Conrad

Abstract

The transient and stable expression of potentially therapeutic proteins in plants is a promising tool for the efficient production of vaccines and antibodies at low cost connected with a practically unlimited scale-up. To achieve these goals, two major challenges, inadequate production levels and non-scalable purification technologies, have to be overcome. Here we present and discuss protocols enabling to perform influenza vaccine production by transient expression in tobacco plants, to perform analytical experiments as Western blot, ELISA, and hemagglutination assays and to purify the antigens by classical affinity chromatography and scalable membrane-based Inverse Transition Cycling.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 17 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 17 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 18%
Student > Doctoral Student 2 12%
Student > Bachelor 2 12%
Professor 2 12%
Lecturer 1 6%
Other 2 12%
Unknown 5 29%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 6 35%
Pharmacology, Toxicology and Pharmaceutical Science 1 6%
Nursing and Health Professions 1 6%
Economics, Econometrics and Finance 1 6%
Decision Sciences 1 6%
Other 1 6%
Unknown 6 35%