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NF-kappa B

Overview of attention for book
Cover of 'NF-kappa B'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Electrophoretic Mobility Shift Assay Analysis of NF-κB DNA Binding.
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    Chapter 2 Detection of IκB Degradation Dynamics and IκB-α Ubiquitination.
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    Chapter 3 Measurement of NF-κB Transcriptional Activity and Identification of NF-κB cis-Regulatory Elements Using Luciferase Assays.
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    Chapter 4 Assessing Sites of NF-κB DNA Binding Using Chromatin Immunoprecipitation.
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    Chapter 5 IKK Kinase Assay for Assessment of Canonical NF-κB Activation in Neurons.
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    Chapter 6 Analysis of Epidermal Growth Factor-Induced NF-κB Signaling.
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    Chapter 7 Methods to Assess the Activation of the Alternative (Noncanonical) NF-κB Pathway by Non-death TNF Receptors.
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    Chapter 8 Systematic Detection of Noncanonical NF-κB Activation.
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    Chapter 9 Noncanonical NF-κB Activation and SDF-1 Expression in Human Endothelial Cells.
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    Chapter 10 Stable Reconstitution of IKK-Deficient Mouse Embryonic Fibroblasts.
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    Chapter 11 Dissecting NF-κB Signaling Induced by Genotoxic Agents via Genetic Complementation of NEMO-Deficient 1.3E2 Cells.
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    Chapter 12 Visualizing TCR-Induced POLKADOTS Formation and NF-κB Activation in the D10 T-Cell Clone and Mouse Primary Effector T Cells.
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    Chapter 13 Detection of Recombinant and Cellular MALT1 Paracaspase Activity.
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    Chapter 14 TRAF Protein Function in Noncanonical NF-κB Signaling.
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    Chapter 15 Roles of c-IAP Proteins in TNF Receptor Family Activation of NF-κB Signaling.
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    Chapter 16 Elucidating Dynamic Protein-Protein Interactions and Ubiquitination in NF-κB Signaling Pathways.
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    Chapter 17 Immunoblot Analysis of Linear Polyubiquitination of NEMO.
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    Chapter 18 In Vitro Detection of NEMO–Ubiquitin Binding Using DELFIA and Microscale Thermophoresis Assays
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    Chapter 19 Use of Fluorescence Spectroscopy for Quantitative Investigations of Ubiquitin Interactions with the Ubiquitin-Binding Domains of NEMO.
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    Chapter 20 Generation of a Proteolytic Signal: E3/E2-Mediated Polyubiquitination of IκBα.
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    Chapter 21 Control of NF-κB Subunits by Ubiquitination.
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    Chapter 22 Methodology to Study NF-κB/RelA Ubiquitination In Vivo.
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    Chapter 23 Using Sequential Immunoprecipitation and Mass Spectrometry to Identify Methylation of NF-κB.
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    Chapter 24 Methods to Detect NF-κB Acetylation and Methylation.
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    Chapter 25 A Method for the Quantitative Analysis of Stimulation-Induced Nuclear Translocation of the p65 Subunit of NF-κB from Patient-Derived Dermal Fibroblasts.
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    Chapter 26 Methods for Assessing the In Vitro Transforming Activity of NF-κB Transcription Factor c-Rel and Related Proteins.
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    Chapter 27 Using RNA Interference in Lung Cancer Cells to Target the IKK-NF-κB Pathway.
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    Chapter 28 Immunohistochemical Analysis of NF-κB in Human Tumor Tissue.
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    Chapter 29 Assessment of Canonical NF-κB Activity in Canine Diffuse Large B-Cell Lymphoma.
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    Chapter 30 NEMO-Binding Domain Peptide Inhibition of Inflammatory Signal-Induced NF-κB Activation In Vivo.
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    Chapter 31 Regulation of NF-κB Signaling in Osteoclasts and Myeloid Progenitors.
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    Chapter 32 NF-κB Activation with Aging: Characterization and Therapeutic Inhibition.
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    Chapter 33 The "Sneaking-Ligand" Approach: Cell-Type Specific Inhibition of the Classical NF-κB Pathway.
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    Chapter 34 Sneaking-Ligand Fusion Proteins Attenuate Serum Transfer Arthritis by Endothelium-Targeted NF-κB Inhibition.
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    Chapter 35 Analysis of NF-κB Activation in Mouse Intestinal Epithelial Cells.
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    Chapter 36 Characterizing the DNA Binding Site Specificity of NF-κB with Protein-Binding Microarrays (PBMs).
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    Chapter 37 Methods for Analyzing the Evolutionary Relationship of NF-κB Proteins Using Free, Web-Driven Bioinformatics and Phylogenetic Tools.
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    Chapter 38 Studying NF-κB Signaling with Mathematical Models.
Attention for Chapter 3: Measurement of NF-κB Transcriptional Activity and Identification of NF-κB cis-Regulatory Elements Using Luciferase Assays.
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Chapter title
Measurement of NF-κB Transcriptional Activity and Identification of NF-κB cis-Regulatory Elements Using Luciferase Assays.
Chapter number 3
Book title
NF-kappa B
Published in
Methods in molecular biology, February 2015
DOI 10.1007/978-1-4939-2422-6_3
Pubmed ID
Book ISBNs
978-1-4939-2421-9, 978-1-4939-2422-6
Authors

Patricia E Collins, Christine O'Carroll, Ruaidhrí J Carmody, Patricia E. Collins, Christine O’Carroll, Ruaidhrí J. Carmody, Collins, Patricia E., O’Carroll, Christine, Carmody, Ruaidhrí J.

Editors

Michael J. May

Abstract

The NF-κB family of transcription factors is activated in response to numerous environmental stimuli and coordinates the transcriptional response to immunoreceptors such as the Toll-like receptors, cytokine receptors, and antigen receptors, growth factors, survival factors, and stress signals such as ultraviolet irradiation and oxidative stress. The transcriptional targets of these various pathways include approximately 500 experimentally indentified genes, and it is highly likely that many others remain to be discovered. A genome-wide analysis of NF-κB-chromatin interactions has revealed a surprisingly large number of NF-κB binding sites across the entire genome, many of which are found in intergenic regions and many more do not appear to be associated with changes in transcription of nearby genes. Assessing the consequences of NF-κB binding at genomic sites is therefore essential to determine the functional role of NF-κB in regulating the expression of specific genes. Luciferase-based reporter assays provide a robust and flexible method to test the contribution of specific NF-κB sites to the regulation of gene transcription. The methods described in this chapter may be applied to any promoter sequence and used in a variety of cell lines and conditions to provide critical information on the regulation of gene expression by NF-κB.

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X Demographics

The data shown below were collected from the profiles of 2 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 11 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 11 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 27%
Researcher 3 27%
Student > Bachelor 1 9%
Unknown 4 36%
Readers by discipline Count As %
Agricultural and Biological Sciences 3 27%
Biochemistry, Genetics and Molecular Biology 2 18%
Veterinary Science and Veterinary Medicine 1 9%
Neuroscience 1 9%
Unknown 4 36%
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 05 March 2015.
All research outputs
#17,749,774
of 22,793,427 outputs
Outputs from Methods in molecular biology
#7,220
of 13,110 outputs
Outputs of similar age
#242,436
of 352,554 outputs
Outputs of similar age from Methods in molecular biology
#421
of 992 outputs
Altmetric has tracked 22,793,427 research outputs across all sources so far. This one is in the 19th percentile – i.e., 19% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,110 research outputs from this source. They receive a mean Attention Score of 3.3. This one is in the 39th percentile – i.e., 39% of its peers scored the same or lower than it.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 352,554 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 27th percentile – i.e., 27% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 992 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 52% of its contemporaries.