↓ Skip to main content

Lipid signaling protocols

Overview of attention for book
Cover of 'Lipid signaling protocols'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Method for Assaying the Lipid Kinase Phosphatidylinositol-5-phosphate 4-kinase α in Quantitative High-Throughput Screening (qHTS) Bioluminescent Format
  3. Altmetric Badge
    Chapter 2 Assaying Ceramide Synthase Activity In Vitro and in Living Cells Using Liquid Chromatography-Mass Spectrometry
  4. Altmetric Badge
    Chapter 3 Lipid Signaling Protocols
  5. Altmetric Badge
    Chapter 4 Identification of the Interactome of a Palmitoylated Membrane Protein, Phosphatidylinositol 4-Kinase Type II Alpha
  6. Altmetric Badge
    Chapter 5 Measurement of Long-Chain Fatty Acyl-CoA Synthetase Activity
  7. Altmetric Badge
    Chapter 6 Qualitative and Quantitative In Vitro Analysis of Phosphatidylinositol Phosphatase Substrate Specificity
  8. Altmetric Badge
    Chapter 7 Luciferase Reporter Assays to Assess Liver X Receptor Transcriptional Activity
  9. Altmetric Badge
    Chapter 8 Metabolically Biotinylated Reporters for Electron Microscopic Imaging of Cytoplasmic Membrane Microdomains
  10. Altmetric Badge
    Chapter 9 Fluorescence Recovery After Photobleaching Analysis of the Diffusional Mobility of Plasma Membrane Proteins: HER3 Mobility in Breast Cancer Cell Membranes.
  11. Altmetric Badge
    Chapter 10 Isolation and Analysis of Detergent-Resistant Membrane Fractions
  12. Altmetric Badge
    Chapter 11 Detection of Isolated Mitochondria-Associated ER Membranes Using the Sigma-1 Receptor
  13. Altmetric Badge
    Chapter 12 Using Surface Plasmon Resonance to Quantitatively Assess Lipid–Protein Interactions
  14. Altmetric Badge
    Chapter 13 Analyzing Protein–Phosphoinositide Interactions with Liposome Flotation Assays
  15. Altmetric Badge
    Chapter 14 High-Throughput Fluorometric Assay for Membrane–Protein Interaction
  16. Altmetric Badge
    Chapter 15 Guidelines for the Use of Protein Domains in Acidic Phospholipid Imaging.
  17. Altmetric Badge
    Chapter 16 Analysis of Sphingolipid Synthesis and Transport by Metabolic Labeling of Cultured Cells with [ 3 H]Serine
  18. Altmetric Badge
    Chapter 17 Determination and Characterization of Tetraspanin-Associated Phosphoinositide-4 Kinases in Primary and Neoplastic Liver Cells
  19. Altmetric Badge
    Chapter 18 Analysis of the Phosphoinositide Composition of Subcellular Membrane Fractions
  20. Altmetric Badge
    Chapter 19 Single-Molecule Imaging of Signal Transduction via GPI-Anchored Receptors
  21. Altmetric Badge
    Chapter 20 Measuring Phosphatidylinositol Generation on Biological Membranes
  22. Altmetric Badge
    Chapter 21 Assay for CDP-Diacylglycerol Generation by CDS in Membrane Fractions
Attention for Chapter 7: Luciferase Reporter Assays to Assess Liver X Receptor Transcriptional Activity
Altmetric Badge

Citations

dimensions_citation
5 Dimensions

Readers on

mendeley
6 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
Luciferase Reporter Assays to Assess Liver X Receptor Transcriptional Activity
Chapter number 7
Book title
Lipid Signaling Protocols
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3170-5_7
Pubmed ID
Book ISBNs
978-1-4939-3169-9, 978-1-4939-3170-5
Authors

Matthew C. Gage, Benoit Pourcet, Inés Pineda-Torra

Abstract

Luciferase reporter assays are sensitive and accurate tests that enable the analysis of regulatory sequences, the magnitude of transcriptional activity by transcription factors, and the discovery of gene regulatory elements and small-molecule modulators with high levels of precision. This is made possible through detection of bioluminescence produced by luciferase-coding reporters in a wide range of cellular environments. These assays are routinely used to analyze the activity of transcription factors, including the lipid-activated liver X receptor (LXR), in response to different stimuli as well as for the identification of their ligands. In this chapter we describe in detail the assays performed to investigate LXR activity in a macrophage-like cell line (RAW 267.4). These can be easily adapted to other nuclear receptors and transcription factors.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 2 33%
Unspecified 1 17%
Student > Bachelor 1 17%
Researcher 1 17%
Unknown 1 17%
Readers by discipline Count As %
Immunology and Microbiology 2 33%
Unspecified 1 17%
Agricultural and Biological Sciences 1 17%
Chemistry 1 17%
Unknown 1 17%