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Mammalian Synthetic Promoters

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Cover of 'Mammalian Synthetic Promoters'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Initial Considerations Before Designing a Promoter Construct
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    Chapter 2 Demonstrating Interactions of Transcription Factors with DNA by Electrophoretic Mobility Shift Assay
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    Chapter 3 Chromatin Immunoprecipitation and Quantitative Real-Time PCR to Assess Binding of a Protein of Interest to Identified Predicted Binding Sites Within a Promoter
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    Chapter 4 Secreted Reporters for Monitoring Multiple Promoter Function
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    Chapter 5 Bioluminescence Monitoring of Promoter Activity In Vitro and In Vivo
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    Chapter 6 Monitoring Promoter Activity by Flow Cytometry
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    Chapter 7 Functional Screening of Core Promoter Activity
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    Chapter 8 Bioinformatically Informed Design of Synthetic Mammalian Promoters
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    Chapter 9 Synthetic Tumor-Specific Promoters for Transcriptional Regulation of Viral Replication
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    Chapter 10 Constructing Strong Cell Type-Specific Promoters Through Informed Design
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    Chapter 11 PCR Assembly of Synthetic Promoters
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    Chapter 12 The Tetracycline Responsive System
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    Chapter 13 Light-Responsive Promoters
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    Chapter 14 A Simple Method for Constructing Artificial Promoters Activated in Response to Ultrasound Stimulation
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    Chapter 15 Promoter Activation with Electromagnetism
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    Chapter 16 Application of Synthetic Tumor-Specific Promoters Responsive to the Tumor Microenvironment
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    Chapter 17 Improving water-use efficiency by decreasing stomatal conductance and transpiration rate to maintain higher ear photosynthetic rate in drought-resistant wheat
  19. Altmetric Badge
    Chapter 18 Computational Sequence Design with R2oDNA Designer
  20. Altmetric Badge
    Chapter 19 Design of Synthetic Promoters for Gene Circuits in Mammalian Cells
Attention for Chapter 6: Monitoring Promoter Activity by Flow Cytometry
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Chapter title
Monitoring Promoter Activity by Flow Cytometry
Chapter number 6
Book title
Mammalian Synthetic Promoters
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-7223-4_6
Pubmed ID
Book ISBNs
978-1-4939-7221-0, 978-1-4939-7223-4
Authors

Taher E. I. Taher, Taher, Taher E. I.

Abstract

Genetic reporters have become invaluable tools for indirectly monitoring promoter activities. The quantitative measurement of promoter activities using reporter gene systems is fundamental for pharmaceutical, biomedical, and molecular biology research. Genetic reporters are used not only for measuring promoter activities but also for understanding the mechanisms controlling gene transcription and in the identification, and characterization of cis-acting regulatory elements. Fluorescent reporter proteins including enhanced green fluorescent protein (EGFP ) are reliable for monitoring quantitative underlying differences in promoter activities. The emitted fluorescence intensity of the expressed reporter is measured at the single-cell level by flow cytometry and represents a readout for the promoter activities. In this chapter, the protocol for measurement and analyzing of transfected cells expressing the reporter gene EGFP is thoroughly described and fully illustrated.

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Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 1 100%
Readers by discipline Count As %
Agricultural and Biological Sciences 1 100%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 08 November 2021.
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#22,066,184
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#10,665
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