↓ Skip to main content

The Retinoblastoma Protein

Overview of attention for book
Cover of 'The Retinoblastoma Protein'

Table of Contents

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

Readers on

mendeley
15 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
Detection of E2F-Induced Transcriptional Activity Using a Dual Luciferase Reporter Assay
Chapter number 14
Book title
The Retinoblastoma Protein
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7565-5_14
Pubmed ID
Book ISBNs
978-1-4939-7564-8, 978-1-4939-7565-5
Authors

Ainhoa Iglesias-Ara, Nerea Osinalde, Ana M. Zubiaga

Abstract

The E2F transcription factors are key targets for the retinoblastoma (RB) tumor suppressor function. The active or inactive status of RB determines the degree by which E2F-dependent gene expression will occur in a given condition. Changes in transcriptional activity in response to extracellular or intracellular stimuli are frequently measured using genetic reporter assays. In particular, dual luciferase reporter assays are most recommended for this purpose because of their improved experimental accuracy. Here we illustrate the usefulness of the dual luciferase reporter assay to detect E2F-mediated transcriptional activity upon overexpression of E2F1 in cultured cells as readout for RB status and function.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 33%
Lecturer 1 7%
Student > Doctoral Student 1 7%
Librarian 1 7%
Professor 1 7%
Other 3 20%
Unknown 3 20%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 6 40%
Agricultural and Biological Sciences 2 13%
Arts and Humanities 1 7%
Immunology and Microbiology 1 7%
Social Sciences 1 7%
Other 1 7%
Unknown 3 20%