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Argonaute Proteins

Overview of attention for book
Cover of 'Argonaute Proteins'

Table of Contents

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    Book Overview
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    Chapter 1 Purification of Native Argonaute Complexes from the Fission Yeast Schizosaccharomyces pombe
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    Chapter 2 Chromatin Immunoprecipitation in Fission Yeast
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    Chapter 3 Biochemical analyzes of endogenous argonaute complexes immunopurified with anti-Argonaute monoclonal antibodies.
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    Chapter 4 Mapping of Ago2–GW182 Functional Interactions
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    Chapter 5 Continuous Density Gradients to Study Argonaute and GW182 Complexes Associated with the Endocytic Pathway
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    Chapter 6 In Vitro RISC Cleavage Assay
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    Chapter 7 Native Gel Analysis for RISC Assembly
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    Chapter 8 Purification and Assembly of Human Argonaute, Dicer, and TRBP Complexes
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    Chapter 9 Detection of Human Dicer and Argonaute 2 Catalytic Activity
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    Chapter 10 Imaging the Cellular Dynamics of Drosophila Argonaute Proteins
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    Chapter 11 Live Cell Imaging of Argonaute Proteins in Mammalian Cells
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    Chapter 12 Reporter-Based Assays for Analyzing RNA Interference in Mammalian Cells
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    Chapter 13 Artificial Tethering of Argonaute Proteins for Studying their Role in Translational Repression of Target mRNAs
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    Chapter 14 An Efficient System for Let-7 MicroRNA and GW182 Protein-Mediated Deadenylation In Vitro
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    Chapter 15 Cell-Free microRNA-Mediated Translation Repression in Caenorhabditis elegans
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    Chapter 16 Argonaute pull-down and RISC analysis using 2'-O-methylated oligonucleotides affinity matrices.
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    Chapter 17 Cloning Argonaute-associated small RNAs from Caenorhabditis elegans.
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    Chapter 18 Immunoprecipitation of piRNPs and Directional, Next Generation Sequencing of piRNAs
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    Chapter 19 Generation of an Inducible Mouse ES Cell Lines Deficient for Argonaute Proteins
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    Chapter 20 Whole Cell Proteome Regulation by MicroRNAs Captured in a Pulsed SILAC Mass Spectrometry Approach
Attention for Chapter 3: Biochemical analyzes of endogenous argonaute complexes immunopurified with anti-Argonaute monoclonal antibodies.
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  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (90th percentile)
  • High Attention Score compared to outputs of the same age and source (93rd percentile)

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Chapter title
Biochemical analyzes of endogenous argonaute complexes immunopurified with anti-Argonaute monoclonal antibodies.
Chapter number 3
Book title
Argonaute Proteins
Published in
Methods in molecular biology, January 2011
DOI 10.1007/978-1-61779-046-1_3
Pubmed ID
Book ISBNs
978-1-61779-045-4, 978-1-61779-046-1
Authors

Keita Miyoshi, Tomoko N. Okada, Haruhiko Siomi, Mikiko C. Siomi, Miyoshi, Keita, Okada, Tomoko N., Siomi, Haruhiko, Siomi, Mikiko C.

Abstract

Argonaute proteins are key factors in RNA silencing. After association with small RNAs of 20-30 -nucleotides, Argonaute proteins are targeted to homologous RNA molecules that are to be silenced. To understand the functional contributions of Argonaute proteins to RNA silencing at a biochemical level, immunoisolation of Argonaute proteins from living cells of various organisms has been performed. This has enabled the analysis of Argonaute-associated proteins and RNAs. Identifying the small RNAs that associate with individual Argonaute proteins, for instance, could help to elucidate the silencing pathways in which particular Argonaute proteins are involved. However, it is also necessary to note that the results obtained through such biochemical analyzes are greatly affected by the quality and properties of the antibodies used, as well as by the immunoprecipitation conditions employed, including buffer contents and/or salt concentration. In this chapter, we describe fundamental methods for immunoprecipitating Argonaute proteins using monoclonal antibodies as well as for detecting associated proteins and small RNAs. Furthermore, we will also explain how various parameters, such as antibody properties and buffer conditions, can alter the production and interpretation of experimental data.

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X Demographics

The data shown below were collected from the profile of 1 X user 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 23 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 23 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 26%
Professor > Associate Professor 3 13%
Student > Ph. D. Student 2 9%
Professor 1 4%
Unspecified 1 4%
Other 2 9%
Unknown 8 35%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 30%
Agricultural and Biological Sciences 5 22%
Mathematics 1 4%
Unspecified 1 4%
Engineering 1 4%
Other 0 0%
Unknown 8 35%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 11. 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 18 August 2022.
All research outputs
#2,869,359
of 23,122,481 outputs
Outputs from Methods in molecular biology
#553
of 13,270 outputs
Outputs of similar age
#17,586
of 182,045 outputs
Outputs of similar age from Methods in molecular biology
#14
of 230 outputs
Altmetric has tracked 23,122,481 research outputs across all sources so far. Compared to these this one has done well and is in the 87th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 13,270 research outputs from this source. They receive a mean Attention Score of 3.4. This one has done particularly well, scoring higher than 95% of its peers.
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 182,045 tracked outputs that were published within six weeks on either side of this one in any source. This one has done particularly well, scoring higher than 90% of its contemporaries.
We're also able to compare this research output to 230 others from the same source and published within six weeks on either side of this one. This one has done particularly well, scoring higher than 93% of its contemporaries.