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The Genetic Manipulation of Staphylococci

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Cover of 'The Genetic Manipulation of Staphylococci'

Table of Contents

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    Book Overview
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    Chapter 180 Restriction-Modification Systems as a Barrier for Genetic Manipulation of Staphylococcus aureus.
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    Chapter 181 The Genetic Manipulation of Staphylococci
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    Chapter 182 Splicing by Overlap Extension PCR to Obtain Hybrid DNA Products
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    Chapter 183 Method for Preparation and Electroporation of S. aureus and S. epidermidis
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    Chapter 184 Rapid Isolation of DNA from Staphylococcus
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    Chapter 185 Bacteriophage Transduction in Staphylococcus aureus: Broth-Based Method.
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    Chapter 186 Bacteriophage Transduction in Staphylococcus aureus.
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    Chapter 187 Allelic Exchange.
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    Chapter 188 Creation of Staphylococcal Mutant Libraries Using Transposon Tn917.
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    Chapter 189 Generation of a Transposon Mutant Library in Staphylococcus aureus and Staphylococcus epidermidis Using bursa aurealis
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    Chapter 190 Chemical and UV Mutagenesis.
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    Chapter 191 Pulse Field Gel Electrophoresis.
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    Chapter 192 RNA-Sequencing of Staphylococcus aureus Messenger RNA.
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    Chapter 193 Quantitative Real-Time PCR (qPCR) Workflow for Analyzing Staphylococcus aureus Gene Expression.
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    Chapter 275 De Novo Assembly of Plasmids Using Yeast Recombinational Cloning.
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    Chapter 276 The Genetic Manipulation of Staphylococci
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    Chapter 277 Electrophoretic Mobility Shift Assays
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    Chapter 281 Batch Transduction of Transposon Mutant Libraries for Rapid Phenotype Screening in Staphylococcus
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    Chapter 282 Rapid Amplification of cDNA Ends for RNA Transcript Sequencing in Staphylococcus
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    Chapter 283 The Genetic Manipulation of Staphylococci
Attention for Chapter 277: Electrophoretic Mobility Shift Assays
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Chapter title
Electrophoretic Mobility Shift Assays
Chapter number 277
Book title
The Genetic Manipulation of Staphylococci
Published in
Methods in molecular biology, July 2015
DOI 10.1007/7651_2015_277
Pubmed ID
Book ISBNs
978-1-4939-3157-6, 978-1-4939-3158-3
Authors

Sarah E. Rowe, James P. O’Gara, Rowe, Sarah E., O’Gara, James P.

Abstract

Experimental demonstration of regulatory protein interactions with the sequences upstream of potential target genes is an important element in gene expression studies. These experiments termed electrophoretic mobility shift assays (EMSAs) provide valuable insight into the mechanism of action of transcription factors. EMSAs combined with downstream applications such as transcriptional analysis help uncover precisely how regulatory proteins control target gene expression. This chapter comprises a guideline for expression and purification of recombinant transcription factor proteins followed by a detailed protocol for EMSAs.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 241 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 5 2%
India 3 1%
United Kingdom 2 <1%
Bolivia, Plurinational State of 1 <1%
South Africa 1 <1%
Chile 1 <1%
Switzerland 1 <1%
Spain 1 <1%
Canada 1 <1%
Other 0 0%
Unknown 225 93%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 75 31%
Student > Bachelor 36 15%
Researcher 33 14%
Student > Master 26 11%
Student > Doctoral Student 10 4%
Other 35 15%
Unknown 26 11%
Readers by discipline Count As %
Agricultural and Biological Sciences 110 46%
Biochemistry, Genetics and Molecular Biology 59 24%
Medicine and Dentistry 13 5%
Chemistry 10 4%
Immunology and Microbiology 6 2%
Other 11 5%
Unknown 32 13%