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The Retinoblastoma Protein

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Cover of 'The Retinoblastoma Protein'

Table of Contents

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    Book Overview
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    Chapter 1 Characterization of RB1 Deletions in Interphase and Metaphase by Molecular Cytogenetics Exemplified in Chronic Lymphatic Leukemia
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    Chapter 2 Detection of RB1 Gene Copy Number Variations Using a Multiplex Ligation-Dependent Probe Amplification Method
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    Chapter 3 A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 Gene
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    Chapter 4 Using Methylation-Specific PCR to Study RB1 Promoter Hypermethylation
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    Chapter 5 Detection of Aberrant DNA Methylation Patterns in the RB1 Gene
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    Chapter 6 Detection of Retinoblastoma Protein Phosphorylation by Immunoblot Analysis
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    Chapter 7 Immunohistochemical Detection of the Retinoblastoma Protein
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    Chapter 8 Immunohistochemical Detection of Retinoblastoma Protein Phosphorylation in Human Tumor Samples
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    Chapter 9 Detection of CCND1 Locus Amplification by Fluorescence In Situ Hybridization
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    Chapter 10 Detection of CCND1 Gene Copy Number Variations Using Multiplex Ligation-Dependent Probe Amplification and Fluorescence In Situ Hybridization Methods
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    Chapter 11 Detection of p16 Promoter Hypermethylation by Methylation-Specific PCR
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    Chapter 12 Immunohistochemical Detection of p16 in Clinical Samples
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    Chapter 13 Detection of E2F-DNA Complexes Using Chromatin Immunoprecipitation Assays
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    Chapter 14 Detection of E2F-Induced Transcriptional Activity Using a Dual Luciferase Reporter Assay
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    Chapter 15 Detection of HPV E6/E7 mRNA in Clinical Samples Using RNA In Situ Hybridization
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    Chapter 16 CRISPR/Cas9-Mediated Knockout of Rb1 in Xenopus tropicalis
Attention for Chapter 3: A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 Gene
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Chapter title
A Fluorescent Quantitative Multiplex PCR Method to Detect Copy Number Changes in the RB1 Gene
Chapter number 3
Book title
The Retinoblastoma Protein
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7565-5_3
Pubmed ID
Book ISBNs
978-1-4939-7564-8, 978-1-4939-7565-5
Authors

Chitra Kannabiran

Abstract

Copy number changes comprising deletions or insertions involving single or multiple exons of a gene are known to occur in a significant proportion of cases in retinoblastoma. The protocol described here involves a two-step quantitative multiplex PCR process which is suitable for the detection of such mutations in the RB1 as well as in other genes. This is achieved through the use of suitable gene-specific primers designed to amplify individual exons, with universal tags attached to the 5' end of each primer. These tagged primers are used in the first step of PCR of the RB1 gene in patients. The second step is carried out through the use of "universal" primers complementary to the tag sequences alone. This technique facilitates the detection of fluorescent PCR products from multiple exons through the use of a single fluorescent tagged primer.

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Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Lecturer 1 33%
Student > Master 1 33%
Unknown 1 33%
Readers by discipline Count As %
Neuroscience 1 33%
Medicine and Dentistry 1 33%
Unknown 1 33%