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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 7: A Double-Sandwich ELISA for Identification of Monoclonal Antibodies Suitable for Sandwich Immunoassays
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Chapter title
A Double-Sandwich ELISA for Identification of Monoclonal Antibodies Suitable for Sandwich Immunoassays
Chapter number 7
Book title
ELISA
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2742-5_7
Pubmed ID
Book ISBNs
978-1-4939-2741-8, 978-1-4939-2742-5
Authors

Larry H. Stanker, Robert M. Hnasko, Stanker, Larry H., Hnasko, Robert M.

Abstract

The sandwich immunoassay (sELISA) is an invaluable technique for concentrating, detecting, and quantifying target antigens. The two critical components required are a capture antibody and a detection antibody, each binding a different epitope on the target antigen. The specific antibodies incorporated into the test define most of the performance parameters of any subsequent immunoassay regardless of the assay format: traditional ELISA, lateral-flow immunoassay, various bead-based assays, antibody-based biosensors, or the reporting label. Here we describe an approach for identifying monoclonal antibodies (mAbs) suitable for use as capture antibodies and detector antibodies in a sELISA targeting bacterial protein toxins. The approach was designed for early identification of monoclonal antibodies (mAbs), in the initial hybridoma screen.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 53 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 53 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 13 25%
Student > Master 7 13%
Researcher 6 11%
Student > Doctoral Student 4 8%
Student > Ph. D. Student 2 4%
Other 2 4%
Unknown 19 36%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 11 21%
Medicine and Dentistry 5 9%
Pharmacology, Toxicology and Pharmaceutical Science 5 9%
Engineering 5 9%
Environmental Science 1 2%
Other 5 9%
Unknown 21 40%