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ELISA

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Cover of 'ELISA'

Table of Contents

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    Book Overview
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    Chapter 1 The Biochemical Properties of Antibodies and Their Fragments
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    Chapter 2 Hybridoma Technology
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    Chapter 3 Affinity Purification of Antibodies
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    Chapter 4 Bioconjugation of Antibodies to Horseradish Peroxidase (HRP)
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    Chapter 5 Indirect ELISA
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    Chapter 6 Direct ELISA
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    Chapter 7 A Double-Sandwich ELISA for Identification of Monoclonal Antibodies Suitable for Sandwich Immunoassays
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    Chapter 8 ELISpot and DC-ELISpot Assay to Measure Frequency of Antigen-Specific IFNγ-Secreting Cells.
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    Chapter 9 The Western Blot
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    Chapter 10 ELISA
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    Chapter 11 Multiplexed Microsphere Suspension Array-Based Immunoassays
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    Chapter 12 Multiplex Immunoassay: A Planar Array on a Chip Using the MagArray(™) Technology.
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    Chapter 13 Lateral Flow Immunoassay
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    Chapter 14 Immuno-PCR Assay for Sensitive Detection of Proteins in Real Time
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    Chapter 15 ELISA
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    Chapter 16 Tyramide Signal Amplification for Immunofluorescent Enhancement
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    Chapter 17 Correlative Microscopy for Localization of Proteins In Situ: Pre-embedding Immuno-Electron Microscopy Using FluoroNanogold, Gold Enhancement, and Low-Temperature Resin
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    Chapter 18 Multiplex ELISA Using Oligonucleotide Tethered Antibodies.
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    Chapter 19 Gas Plasma Surface Chemistry for Biological Assays
Attention for Chapter 16: Tyramide Signal Amplification for Immunofluorescent Enhancement
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Chapter title
Tyramide Signal Amplification for Immunofluorescent Enhancement
Chapter number 16
Book title
ELISA
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2742-5_16
Pubmed ID
Book ISBNs
978-1-4939-2741-8, 978-1-4939-2742-5
Authors

Lauren Faget, Thomas S. Hnasko, Faget, Lauren, Hnasko, Thomas S.

Abstract

Enzyme-linked signal amplification is a key technique used to enhance the immunohistochemical detection of protein, mRNA, and other molecular species. Tyramide signal amplification (TSA) is based on a catalytic reporter deposit in close vicinity to the epitope of interest. The advantages of this technique are its simplicity, enhanced sensitivity, high specificity, and compatibility with modern multi-label fluorescent microscopy. Here, we describe the use of a TSA kit to increase the signal of enhanced green fluorescent protein (eGFP) expressed under the control of Slc17a6 regulatory elements in the brain of a transgenic mouse. The labeling procedure consists of 6 basic steps: (1) tissue preparation, (2) blocking of nonspecific epitopes, (3) binding with primary antibody, (4) binding with horseradish peroxidase-conjugated secondary antibody, (5) reacting with fluorescent tyramide substrate, and (6) imaging of the signal. The procedures described herein detail these steps and provide additional guidance and background to assist novice users.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 83 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 1%
Unknown 82 99%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 21 25%
Student > Bachelor 9 11%
Researcher 9 11%
Student > Master 7 8%
Student > Postgraduate 4 5%
Other 7 8%
Unknown 26 31%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 15 18%
Agricultural and Biological Sciences 9 11%
Neuroscience 7 8%
Immunology and Microbiology 6 7%
Medicine and Dentistry 6 7%
Other 12 14%
Unknown 28 34%