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Xylem

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Cover of 'Xylem'

Table of Contents

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    Book Overview
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    Chapter 1 Experimental and Theoretical Methods to Approach the Study of Vascular Patterning in the Plant Shoot.
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    Chapter 2 Strigolactone-mediated Stimulation of Secondary Xylem Proliferation in Stems.
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    Chapter 3 Quick Histochemical Staining Methods to Detect Cell Death in Xylem Elements of Plant Tissues.
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    Chapter 4 Establishment and Utilization of Habituated Cell Suspension Cultures for Hormone-Inducible Xylogenesis.
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    Chapter 5 Tissue Culture for Xylem Differentiation with Arabidopsis Leaves.
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    Chapter 6 VND6-induced Xylem Cell Differentiation in Arabidopsis Cell Cultures.
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    Chapter 7 Live Imaging of Developing Xylem In Planta.
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    Chapter 8 Immunolocalization in Secondary Xylem of Populus.
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    Chapter 9 Xylem
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    Chapter 10 Vascular Morphodynamics During Secondary Growth.
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    Chapter 11 Xylem Characterization Using Improved Pseudo-Schiff Propidium Iodide Staining of Whole Mount Samples and Confocal Laser-Scanning Microscopy.
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    Chapter 12 Chemical Imaging of Xylem by Raman Microspectroscopy.
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    Chapter 13 Using CellProfiler to Analyze and Quantify Vascular Morphology.
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    Chapter 14 Lignin Analysis by HPLC and FTIR.
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    Chapter 15 Carbohydrate Composition Analysis in Xylem.
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    Chapter 16 Structural Analysis of Cell Wall Polysaccharides Using PACE.
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    Chapter 17 Analysis of Lignin Composition and Distribution Using Fluorescence Laser Confocal Microspectroscopy.
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    Chapter 18 Topochemical Analysis of Cell Wall Components by TOF-SIMS.
Attention for Chapter 12: Chemical Imaging of Xylem by Raman Microspectroscopy.
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Chapter title
Chemical Imaging of Xylem by Raman Microspectroscopy.
Chapter number 12
Book title
Xylem
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6722-3_12
Pubmed ID
Book ISBNs
978-1-4939-6720-9, 978-1-4939-6722-3
Authors

András Gorzsás

Editors

Miguel de Lucas, J. Peter Etchhells

Abstract

Raman microspectroscopic techniques provide highly detailed chemical information about xylem tissue at submicron spatial resolution. The techniques are generally sensitive and they provide a powerful, yet inexpensive way to probe the chemical composition of individual cells or cell wall layers in situ, non-destructively, in a confocal manner, simultaneously detecting all chemical compounds without the need of external agents (label, dyes, stains). Problems with limited specificity in complex chemical matrices such as cell walls may arise, compounded by fluorescence problems. However, these can often be circumvented. In this chapter, the basics of the technique, including a common instrumental setup, together with the general strengths and limitations of Raman microspectroscopy are discussed. Detailed protocols are provided for single point measurements, as well as for fully customizable raster scan mapping, including sample preparation, setup, and measurement steps. The major steps of the data analysis procedure are discussed as well.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 2 18%
Researcher 2 18%
Lecturer 1 9%
Student > Doctoral Student 1 9%
Other 1 9%
Other 1 9%
Unknown 3 27%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 27%
Agricultural and Biological Sciences 1 9%
Chemistry 1 9%
Medicine and Dentistry 1 9%
Unknown 5 45%