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Telomeres and Telomerase

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Cover of 'Telomeres and Telomerase'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction to Telomeres and Telomerase
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    Chapter 2 Analysis of Average Telomere Length in Human Telomeric Protein Knockout Cells Generated by CRISPR/Cas9
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    Chapter 3 Telomere Length Analysis by Quantitative Fluorescent in Situ Hybridization (Q-FISH)
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    Chapter 4 Telomere Strand-Specific Length Analysis by Fluorescent In Situ Hybridization (Q-CO-FISH)
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    Chapter 5 Telomere G-Rich Overhang Length Measurement: DSN Method
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    Chapter 6 Telomere G-Overhang Length Measurement Method 2: G-Tail Telomere HPA
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    Chapter 7 Telomere Terminal G/C Strand Synthesis: Measuring Telomerase Action and C-Rich Fill-In
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    Chapter 8 Analysis of Yeast Telomerase by Primer Extension Assays
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    Chapter 9 Assessing Telomerase Activities in Mammalian Cells Using the Quantitative PCR-Based Telomeric Repeat Amplification Protocol (qTRAP)
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    Chapter 10 Telomeres and NextGen CO-FISH: Directional Genomic Hybridization (Telo-dGH™)
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    Chapter 11 Visualization of Human Telomerase Localization by Fluorescence Microscopy Techniques
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    Chapter 12 Cytogenetic Analysis of Telomere Dysfunction
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    Chapter 13 Probing the Telomere Damage Response
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    Chapter 14 Induction of Site-Specific Oxidative Damage at Telomeres by Killerred-Fused Shelretin Proteins
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    Chapter 15 Using Protein-Fragment Complementation Assays (PCA) and Peptide Arrays to Study Telomeric Protein-Protein Interactions
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    Chapter 16 In Vitro Preparation and Crystallization of Vertebrate Telomerase Subunits
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    Chapter 17 Human Telomeric G-Quadruplex Structures and G-Quadruplex-Interactive Compounds
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    Chapter 18 Analysis of Telomere-Homologous DNA with Different Conformations Using 2D Agarose Electrophoresis and In-Gel Hybridization
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    Chapter 19 Analysis of Telomere Proteins by Chromatin Immunoprecipitation (ChIP)
Attention for Chapter 9: Assessing Telomerase Activities in Mammalian Cells Using the Quantitative PCR-Based Telomeric Repeat Amplification Protocol (qTRAP)
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Chapter title
Assessing Telomerase Activities in Mammalian Cells Using the Quantitative PCR-Based Telomeric Repeat Amplification Protocol (qTRAP)
Chapter number 9
Book title
Telomeres and Telomerase
Published in
Methods in molecular biology, March 2017
DOI 10.1007/978-1-4939-6892-3_9
Pubmed ID
Book ISBNs
978-1-4939-6891-6, 978-1-4939-6892-3
Authors

Shuai Jiang, Mengfan Tang, Huawei Xin, Junjiu Huang

Editors

Zhou Songyang

Abstract

Telomerase expression and activity appear elevated in >80% of human cancers. The activity of the telomerase may serve as a diagnostic marker for malignancy, and an indicator of the proliferative potential of somatic and stem cells. The telomeric repeat amplification protocol (TRAP) is a sensitive and accurate PCR-based assay for telomerase detection and measurement. Here, we describe a quantitative PCR-based TRAP assay (qTRAP) that is more convenient and amenable to high-throughput applications compared to traditional gel-based TRAP assays. qTRAP can not only facilitate drug screening processes for compounds that regulate telomerase activities but also enable the measurement of total telomerase activities of cultured cells or clinical specimens; the latter should prove particularly valuable to investigators of malignancies and diseases that are associated with telomerase and telomere dysfunction.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 14 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 21%
Student > Bachelor 2 14%
Student > Doctoral Student 2 14%
Student > Master 2 14%
Professor > Associate Professor 1 7%
Other 0 0%
Unknown 4 29%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 6 43%
Nursing and Health Professions 1 7%
Medicine and Dentistry 1 7%
Engineering 1 7%
Unknown 5 36%