Trinucleotide Repeat Protocols

Two decades have passed since trinucleotide repeat expansion was first discovered in genes responsible for certain neurological diseases. Since then, new technologies have developed and innovative concepts have emerged, which may prove useful in devising therapeutic approaches to neurological diseases. Divided into six convenient sections, Trinucleotide Repeat Protocols, Second Edition covers a wide range of topics such as an overview of trinucleotide repeat diseases, synaptic plasticity, embryonic stem (ES) cell-related protocols with a focus on HD, RNA-related protocols, and analysis of epigenetic modification in fragile X syndrome. This edition focuses not only on direct analysis of trinucleotide repeat diseases but also on alternative approaches for the analysis of trinucleotide repeat diseases, with the hope that this will result in a better understanding of the mechanisms and future therapeutic prospects for treatment of these diseases. Written in the successful Methods in Molecular Biology(TM) series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls.

Authoritative and easily accessible, Trinucleotide Repeat Protocols, Second Edition seeks to serve researchers with its thorough methodologies on this expanding field.

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Trinucleotide Repeat Protocols

Two decades have passed since trinucleotide repeat expansion was first discovered in genes responsible for certain neurological diseases. Since then, new technologies have developed and innovative concepts have emerged, which may prove useful in devising therapeutic approaches to neurological diseases. Divided into six convenient sections, Trinucleotide Repeat Protocols, Second Edition covers a wide range of topics such as an overview of trinucleotide repeat diseases, synaptic plasticity, embryonic stem (ES) cell-related protocols with a focus on HD, RNA-related protocols, and analysis of epigenetic modification in fragile X syndrome. This edition focuses not only on direct analysis of trinucleotide repeat diseases but also on alternative approaches for the analysis of trinucleotide repeat diseases, with the hope that this will result in a better understanding of the mechanisms and future therapeutic prospects for treatment of these diseases. Written in the successful Methods in Molecular Biology(TM) series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls.

Authoritative and easily accessible, Trinucleotide Repeat Protocols, Second Edition seeks to serve researchers with its thorough methodologies on this expanding field.

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Trinucleotide Repeat Protocols

Trinucleotide Repeat Protocols

Trinucleotide Repeat Protocols

Trinucleotide Repeat Protocols

Paperback(Softcover reprint of the original 2nd ed. 2013)

$119.99 
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Overview

Two decades have passed since trinucleotide repeat expansion was first discovered in genes responsible for certain neurological diseases. Since then, new technologies have developed and innovative concepts have emerged, which may prove useful in devising therapeutic approaches to neurological diseases. Divided into six convenient sections, Trinucleotide Repeat Protocols, Second Edition covers a wide range of topics such as an overview of trinucleotide repeat diseases, synaptic plasticity, embryonic stem (ES) cell-related protocols with a focus on HD, RNA-related protocols, and analysis of epigenetic modification in fragile X syndrome. This edition focuses not only on direct analysis of trinucleotide repeat diseases but also on alternative approaches for the analysis of trinucleotide repeat diseases, with the hope that this will result in a better understanding of the mechanisms and future therapeutic prospects for treatment of these diseases. Written in the successful Methods in Molecular Biology(TM) series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and notes on troubleshooting and avoiding known pitfalls.

Authoritative and easily accessible, Trinucleotide Repeat Protocols, Second Edition seeks to serve researchers with its thorough methodologies on this expanding field.


Product Details

ISBN-13: 9781493959716
Publisher: Springer-Verlag New York, LLC
Publication date: 08/23/2016
Series: Methods in Molecular Biology , #1010
Edition description: Softcover reprint of the original 2nd ed. 2013
Pages: 296
Product dimensions: 7.01(w) x 10.00(h) x 0.03(d)

Table of Contents

Prefacev
Contributorsix
Part I.Introduction
1Mouse Models of Triplet Repeat Diseases3
Part II.Analysis of Triplet Repeat DNAs and RNAs
2Analysis of Triplet Repeat Replication by Two-Dimensional Gel Electrophoresis19
3Genetic Analysis for Triplet Repeat Instability in Yeast29
4Detection and Isolation of Trinucleotide Repeat Expansions Using the RED Method47
5Analysis of Unstable Triplet Repeats Using Small-Pool Polymerase Chain Reaction61
6Real-Time RT-PCR for CTG Repeat-Containing Genes77
Part III.Detection and Analysis of Polyglutamine-Containing Proteins and Their Aggregates
7Antibodies Against Huntingtin: Production and Screening of Monoclonals and Single-Chain Recombinant Forms87
8Using Antibodies to Analyze Polyglutamine Stretches103
9Solubilization of Aggregates Formed by Expanded Polyglutamine Tract Expression in Cultured Cells129
Part IV.Establishment of Animal and Cultured Cell Models for Trinucleotide Repeat Diseases
10Caenorhabditis elegans as a Model System for Triplet Repeat Diseases141
11Monitoring Aggregate Formation in Organotypic Slice Cultures From Transgenic Mice161
12The CGG Repeat and the FMR1 Gene173
13Analysis of CTG Repeats Using DM1 Model Mice185
14Lentiviral-Mediated Gene Transfer to Model Triplet Repeat Disorders199
15Mouse Tissue Culture Models of Unstable Triplet Repeats215
Part V.In Vivo Analysis of Trinucleotide Repeat Diseases
16Neurotransmitter Receptor Analysis in Transgenic Mouse Models231
17Chromatin Immunoprecipitation Technique for Study of Transcriptional Dysregulation in Intact Mouse Brain261
18Techniques for Thick-Section Golgi Impregnation of Formalin-Fixed Brain Tissue277
19Assessment of Impaired Proteasomal Function in a Cellular Model of Polyglutamine Diseases287
20Assessment of In Vitro and In Vivo Mitochondrial Function in Friedreich's Ataxia and Huntington's Disease293
21Triplet Repeats and DNA Repair: Germ Cell and Somatic Cell Instability in Transgenic Mice309
22Oxidative Damage in Huntington's Disease321
Index335
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