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The Resource Atomic force microscopy for biologists, V.J. Morris, A.R. Kirby, A.P. Gunning

Atomic force microscopy for biologists, V.J. Morris, A.R. Kirby, A.P. Gunning

Label
Atomic force microscopy for biologists
Title
Atomic force microscopy for biologists
Statement of responsibility
V.J. Morris, A.R. Kirby, A.P. Gunning
Creator
Contributor
Subject
Language
eng
Cataloging source
UKM
http://library.link/vocab/creatorName
Morris, V. J
Illustrations
illustrations
Index
index present
Literary form
non fiction
Nature of contents
bibliography
http://library.link/vocab/relatedWorkOrContributorName
  • Kirby, A. R
  • Gunning, A. P
http://library.link/vocab/subjectName
  • Atomic force microscopy
  • Microtechnique
  • Biology
Label
Atomic force microscopy for biologists, V.J. Morris, A.R. Kirby, A.P. Gunning
Instantiates
Publication
Bibliography note
Includes bibliographical references and index
Carrier category
volume
Carrier category code
  • nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Contents
  • Ch. 1.
  • Introduction.
  • p. 1
  • Ch. 2.
  • Apparatus.
  • p. 5
  • 2.1.
  • atomic force microscope.
  • p. 5
  • 2.2.
  • Piezoelectric scanners.
  • p. 8
  • 2.3.
  • Probes and cantilevers.
  • p. 9
  • 2.4.
  • Sample holders.
  • p. 14
  • 2.5.
  • Detection methods.
  • p. 15
  • 2.6.
  • Control systems.
  • p. 21
  • 2.7.
  • Vibration isolation: thermal and mechanical.
  • p. 29
  • 2.8.
  • Calibration.
  • p. 30
  • 2.9.
  • Integrated AFMs.
  • p. 37
  • Ch. 3.
  • Basic Principles.
  • p. 44
  • 3.1.
  • Forces.
  • p. 44
  • 3.2.
  • Imaging modes.
  • p. 50
  • 3.3.
  • Image types.
  • p. 55
  • 3.4.
  • Substrates.
  • p. 57
  • 3.5.
  • Common problems.
  • p. 59
  • 3.6.
  • Getting started.
  • p. 64
  • 3.7.
  • Image optimisation.
  • p. 69
  • Ch. 4.
  • Macromolecules.
  • p. 76
  • 4.1.
  • Imaging methods.
  • p. 76
  • 4.2.
  • Nucleic acids: DNA.
  • p. 88
  • 4.3.
  • Nucleic acids: RNA.
  • p. 104
  • 4.4.
  • Polysaccharides.
  • p. 105
  • 4.5.
  • Proteins.
  • p. 123
  • Ch. 5.
  • Interfacial Systems.
  • p. 160
  • 5.1.
  • Introduction to interfaces.
  • p. 160
  • 5.2.
  • Sample preparation.
  • p. 168
  • 5.3.
  • Phospholipids.
  • p. 172
  • 5.4.
  • Liposomes and intact vesicles.
  • p. 190
  • 5.5.
  • Lipid-protein mixed films.
  • p. 192
  • 5.6.
  • Miscellaneous lipid films.
  • p. 196
  • 5.7.
  • Interfacial protein films.
  • p. 197
  • Ch. 6.
  • Ordered Macromolecules.
  • p. 209
  • 6.1.
  • Three dimensional crystals.
  • p. 209
  • 6.2.
  • Two dimensional protein crystals.
  • p. 217
  • 6.3.
  • AFM studies of 2D membrane protein crystals.
  • p. 224
  • 6.4.
  • AFM studies of 2D crystals of soluble proteins.
  • p. 238
  • Ch. 7.
  • Cells, Tissue and Biominerals.
  • p. 254
  • 7.1.
  • Imaging methods.
  • p. 254
  • 7.2.
  • Microbial cells: bacteria, spores and yeasts.
  • p. 264
  • 7.3.
  • Blood cells.
  • p. 269
  • 7.4.
  • Neurons and Glial cells.
  • p. 273
  • 7.5.
  • Epithelial cells.
  • p. 275
  • 7.6.
  • Non-confluent renal cells.
  • p. 278
  • 7.7.
  • Endothelial cells.
  • p. 279
  • 7.8.
  • Cardiocytes.
  • p. 281
  • 7.9.
  • Other mammalian cells.
  • p. 283
  • 7.10.
  • Plant cells.
  • p. 285
  • 7.11.
  • Tissue.
  • p. 289
  • 7.12.
  • Biominerals.
  • p. 294
  • Ch. 8.
  • Other Probe Microscopes.
  • p. 311
  • 8.1.
  • Overview.
  • p. 311
  • 8.2.
  • Scanning tunnelling microscope (STM).
  • p. 311
  • 8.3.
  • Scanning near-field optical microscope (SNOM).
  • p. 314
  • 8.4.
  • Scanning ion conductance microscope (SICM).
  • p. 317
  • 8.5.
  • Scanning thermal microscope (SThM).
  • p. 318
  • 8.6.
  • Optical tweezers and the photonic force microscope (PFM).
  • p. 319
  • SPM books.
  • p. 323
  • Index.
  • p. 324
Control code
24579984
Dimensions
23 cm.
Extent
xiv, 332 p.
Isbn
9781860941993
Media category
unmediated
Media MARC source
rdamedia
Media type code
  • n
Other physical details
ill.
Label
Atomic force microscopy for biologists, V.J. Morris, A.R. Kirby, A.P. Gunning
Publication
Bibliography note
Includes bibliographical references and index
Carrier category
volume
Carrier category code
  • nc
Carrier MARC source
rdacarrier
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Contents
  • Ch. 1.
  • Introduction.
  • p. 1
  • Ch. 2.
  • Apparatus.
  • p. 5
  • 2.1.
  • atomic force microscope.
  • p. 5
  • 2.2.
  • Piezoelectric scanners.
  • p. 8
  • 2.3.
  • Probes and cantilevers.
  • p. 9
  • 2.4.
  • Sample holders.
  • p. 14
  • 2.5.
  • Detection methods.
  • p. 15
  • 2.6.
  • Control systems.
  • p. 21
  • 2.7.
  • Vibration isolation: thermal and mechanical.
  • p. 29
  • 2.8.
  • Calibration.
  • p. 30
  • 2.9.
  • Integrated AFMs.
  • p. 37
  • Ch. 3.
  • Basic Principles.
  • p. 44
  • 3.1.
  • Forces.
  • p. 44
  • 3.2.
  • Imaging modes.
  • p. 50
  • 3.3.
  • Image types.
  • p. 55
  • 3.4.
  • Substrates.
  • p. 57
  • 3.5.
  • Common problems.
  • p. 59
  • 3.6.
  • Getting started.
  • p. 64
  • 3.7.
  • Image optimisation.
  • p. 69
  • Ch. 4.
  • Macromolecules.
  • p. 76
  • 4.1.
  • Imaging methods.
  • p. 76
  • 4.2.
  • Nucleic acids: DNA.
  • p. 88
  • 4.3.
  • Nucleic acids: RNA.
  • p. 104
  • 4.4.
  • Polysaccharides.
  • p. 105
  • 4.5.
  • Proteins.
  • p. 123
  • Ch. 5.
  • Interfacial Systems.
  • p. 160
  • 5.1.
  • Introduction to interfaces.
  • p. 160
  • 5.2.
  • Sample preparation.
  • p. 168
  • 5.3.
  • Phospholipids.
  • p. 172
  • 5.4.
  • Liposomes and intact vesicles.
  • p. 190
  • 5.5.
  • Lipid-protein mixed films.
  • p. 192
  • 5.6.
  • Miscellaneous lipid films.
  • p. 196
  • 5.7.
  • Interfacial protein films.
  • p. 197
  • Ch. 6.
  • Ordered Macromolecules.
  • p. 209
  • 6.1.
  • Three dimensional crystals.
  • p. 209
  • 6.2.
  • Two dimensional protein crystals.
  • p. 217
  • 6.3.
  • AFM studies of 2D membrane protein crystals.
  • p. 224
  • 6.4.
  • AFM studies of 2D crystals of soluble proteins.
  • p. 238
  • Ch. 7.
  • Cells, Tissue and Biominerals.
  • p. 254
  • 7.1.
  • Imaging methods.
  • p. 254
  • 7.2.
  • Microbial cells: bacteria, spores and yeasts.
  • p. 264
  • 7.3.
  • Blood cells.
  • p. 269
  • 7.4.
  • Neurons and Glial cells.
  • p. 273
  • 7.5.
  • Epithelial cells.
  • p. 275
  • 7.6.
  • Non-confluent renal cells.
  • p. 278
  • 7.7.
  • Endothelial cells.
  • p. 279
  • 7.8.
  • Cardiocytes.
  • p. 281
  • 7.9.
  • Other mammalian cells.
  • p. 283
  • 7.10.
  • Plant cells.
  • p. 285
  • 7.11.
  • Tissue.
  • p. 289
  • 7.12.
  • Biominerals.
  • p. 294
  • Ch. 8.
  • Other Probe Microscopes.
  • p. 311
  • 8.1.
  • Overview.
  • p. 311
  • 8.2.
  • Scanning tunnelling microscope (STM).
  • p. 311
  • 8.3.
  • Scanning near-field optical microscope (SNOM).
  • p. 314
  • 8.4.
  • Scanning ion conductance microscope (SICM).
  • p. 317
  • 8.5.
  • Scanning thermal microscope (SThM).
  • p. 318
  • 8.6.
  • Optical tweezers and the photonic force microscope (PFM).
  • p. 319
  • SPM books.
  • p. 323
  • Index.
  • p. 324
Control code
24579984
Dimensions
23 cm.
Extent
xiv, 332 p.
Isbn
9781860941993
Media category
unmediated
Media MARC source
rdamedia
Media type code
  • n
Other physical details
ill.

Library Locations

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      Ashton Street, Liverpool, L69 3DA, GB
      53.418074 -2.967913
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