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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 7: Immunohistochemical Detection of the Retinoblastoma Protein
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Chapter title
Immunohistochemical Detection of the Retinoblastoma Protein
Chapter number 7
Book title
The Retinoblastoma Protein
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7565-5_7
Pubmed ID
Book ISBNs
978-1-4939-7564-8, 978-1-4939-7565-5
Authors

Charles A. Ishak, Matthew J. Cecchini, Christopher J. Howlett, Frederick A. Dick

Abstract

The retinoblastoma protein (pRB) plays a key role in proliferative control and genome stability. For these reasons its functions are considered to be tumor suppressive. Its functional status offers critical insight into proliferative control signaling in tissues and in developing malignancies. In this chapter, we outline basic procedures to detect the retinoblastoma protein in formalin fixed, paraffin embedded tissue sections. In addition, we provide protocols to detect phosphorylation levels of pRB in tissues and offer controls to ensure fidelity of measurement. Importantly, these staining methods utilize broadly available reagents and equipment making them accessible to most biomedical research laboratories.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 50%
Unspecified 1 25%
Student > Bachelor 1 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 2 50%
Unspecified 1 25%
Unknown 1 25%