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Cryopreservation and Freeze-Drying Protocols

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Cover of 'Cryopreservation and Freeze-Drying Protocols'

Table of Contents

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    Book Overview
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    Chapter 1 Principles of Cryopreservation
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    Chapter 2 Principles of cryopreservation by vitrification.
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    Chapter 3 Modeling and Optimization of Cryopreservation
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    Chapter 4 The Principles of Freeze-Drying
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    Chapter 5 Use of In Situ Fourier Transform Infrared Spectroscopy to Study Freezing and Drying of Cells
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    Chapter 6 Calorimetric Analysis of Cryopreservation and Freeze-Drying Formulations
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    Chapter 7 Measurement of Intracellular Ice Formation Kinetics by High-Speed Video Cryomicroscopy
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    Chapter 8 Laser Scanning Microscopy in Cryobiology
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    Chapter 9 Low-Temperature Electron Microscopy: Techniques and Protocols
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    Chapter 10 Cryopreservation of Semen from Domestic Livestock
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    Chapter 11 Cryopreservation of Mammalian oocytes.
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    Chapter 12 Vitrification: A Simple and Successful Method for Cryostorage of Human Blastocysts
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    Chapter 13 Efficient cryopreservation of human pluripotent stem cells by surface-based vitrification.
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    Chapter 14 Cryopreservation of Greenshell™ Mussel (Perna canaliculus) Sperm
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    Chapter 15 Membrane Modification Strategies for Cryopreservation
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    Chapter 16 Sperm cleanup and centrifugation processing for cryopreservation.
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    Chapter 17 Cryopreservation of Red Blood Cells
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    Chapter 18 Cord Blood Clinical Processing, Cryopreservation, and Storage
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    Chapter 19 Directional Freezing for Large Volume Cryopreservation
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    Chapter 20 Vitrification of heart valve tissues.
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    Chapter 21 Cryopreservation of Plant Cell Lines
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    Chapter 22 Writing Standard Operating Procedures (SOPs) for Cryostorage Protocols: Using Shoot Meristem Cryopreservation as an Example.
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    Chapter 23 Freeze-Drying of Proteins
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    Chapter 24 Freeze-Drying of Lactic Acid Bacteria
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    Chapter 25 Freeze-Drying of Mammalian Sperm
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    Chapter 26 Freeze-Drying of Decellularized Heart Valve Tissues
Attention for Chapter 16: Sperm cleanup and centrifugation processing for cryopreservation.
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Chapter title
Sperm cleanup and centrifugation processing for cryopreservation.
Chapter number 16
Book title
Cryopreservation and Freeze-Drying Protocols
Published in
Methods in molecular biology, November 2014
DOI 10.1007/978-1-4939-2193-5_16
Pubmed ID
Book ISBNs
978-1-4939-2192-8, 978-1-4939-2193-5
Authors

Sieme H, Oldenhof H, Harald Sieme, Harriëtte Oldenhof, Sieme, Harald, Oldenhof, Harriëtte

Abstract

Fertility rates with artificial insemination are highest with good-quality sperm samples. Therefore, nonviable sperm, cellular debris, and seminal plasma are preferably removed from semen samples prior to use or for preservation. Such compounds are sources where reactive oxygen species are generated during storage or upon cryopreservation, impairing sperm function. In this chapter we describe methods to remove seminal plasma and cellular debris from sperm samples, and for selecting morphologically normal motile sperm. The methods that are described here include: ordinary centrifugation, sperm swim-up, glass wool and Sephadex filtration/adherence, and single-layer as well as discontinuous two-layer iodixanol density gradient centrifugation.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 18 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Iran, Islamic Republic of 1 6%
Unknown 17 94%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 28%
Student > Bachelor 3 17%
Student > Master 3 17%
Professor 1 6%
Other 1 6%
Other 2 11%
Unknown 3 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 4 22%
Biochemistry, Genetics and Molecular Biology 4 22%
Veterinary Science and Veterinary Medicine 3 17%
Medicine and Dentistry 3 17%
Physics and Astronomy 1 6%
Other 0 0%
Unknown 3 17%