Handbook of Analysis of Oligonucleotides and Related Products

Author:   Jose V. Bonilla (Girindus America, Cincinnati, Ohio, USA) ,  G. Susan Srivatsa (ElixinPharma, Encinitas, California, USA)
Publisher:   Taylor & Francis Inc
ISBN:  

9781439819937


Pages:   512
Publication Date:   23 February 2011
Format:   Hardback
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

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Handbook of Analysis of Oligonucleotides and Related Products


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Full Product Details

Author:   Jose V. Bonilla (Girindus America, Cincinnati, Ohio, USA) ,  G. Susan Srivatsa (ElixinPharma, Encinitas, California, USA)
Publisher:   Taylor & Francis Inc
Imprint:   CRC Press Inc
Dimensions:   Width: 17.80cm , Height: 2.80cm , Length: 25.40cm
Weight:   1.400kg
ISBN:  

9781439819937


ISBN 10:   1439819939
Pages:   512
Publication Date:   23 February 2011
Audience:   College/higher education ,  Professional and scholarly ,  Tertiary & Higher Education ,  Professional & Vocational
Format:   Hardback
Publisher's Status:   Active
Availability:   In Print   Availability explained
This item will be ordered in for you from one of our suppliers. Upon receipt, we will promptly dispatch it out to you. For in store availability, please contact us.

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Reviews

This is a unique resource for guiding the analysis of oligonucleotide-based drug products. No other single source provides such a comprehensive overview of the necessary analytical techniques that assess the qualitative characteristics of oligonucleotides intended for pharmaceutical use. --Rachel R Chennault, Ph.D.(American College of Clinical Pharmacy), in Doody's Notes


Author Information

Dr. Jose V. Bonilla's career has been dedicated to the introduction and implementation of cutting-edge analytical technologies such as LC-MS, high-speed gas chromatography, high-speed GPC, online GC, online HPLC, and online near-IR. He has extensive experience in the management of industrial and pharmaceutical analytical laboratories in compliance with regulatory requirements and is the author and coauthor of several peer-reviewed publications. Dr. G. Susan Srivatsa has more than 20 years of experience in the development of small molecules, proteins, peptides, and oligonucleotides as therapeutics. She has contributed to the successful development of more than 35 DNA and RNA oligonucleotide drug candidates through various stages of clinical development and has published widely in the area of oligonucleotide analysis in peer-reviewed journals.

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