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Quantitative proteomics using stable isotope labeling with amino acids in cell culture

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Quantitative proteomics using stable isotope labeling with amino acids in cell culture (English)

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H C Harsha

1

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Henrik Molina

series ordinal

2

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Akhilesh Pandey

series ordinal

3

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language of work or name

English

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publication date

2008

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published in

Nature Protocols

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volume

3

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page(s)

505-16

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issue

3

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describes a project that uses

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An integrated mass spectrometry-based proteomic approach: quantitative analysis of tandem affinity-purified in vivo cross-linked protein complexes (QTAX) to decipher the 26 S proteasome-interacting network.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

21 January 2018

Stable isotope labeling by amino acids in cell culture, SILAC, as a simple and accurate approach to expression proteomics

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reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Quantitative analysis of complex protein mixtures using isotope-coded affinity tags

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Protease-catalyzed incorporation of 18O into peptide fragments and its application for protein sequencing by electrospray and matrix-assisted laser desorption/ionization mass spectrometry

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Controlling deuterium isotope effects in comparative proteomics

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Global, in vivo, and site-specific phosphorylation dynamics in signaling networks

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Temporal analysis of phosphotyrosine-dependent signaling networks by quantitative proteomics

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Proteomic Profiling of ClpXP Substrates after DNA Damage Reveals Extensive Instability within SOS Regulon

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reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Biomarker discovery from pancreatic cancer secretome using a differential proteomic approach

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Properties of 13C-Substituted Arginine in Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC)

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Large-scale phosphorylation analysis of mouse liver

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reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Immunoaffinity profiling of tyrosine phosphorylation in cancer cells

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Isolation of phosphoproteins by immobilized metal (Fe3+) affinity chromatography

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Highly selective enrichment of phosphorylated peptides from peptide mixtures using titanium dioxide microcolumns.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FNPROT.2008.2

retrieved

31 March 2020

Identifiers

DOI

10.1038/NPROT.2008.2

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3555198

Dimensions Publication ID

1007381236

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OpenCitations bibliographic resource ID

3555198

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3555198

ResearchGate publication ID

5528165

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Springer Nature article ID

10.1038/nprot.2008.2

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(Q28271745)

Quantitative proteomics using stable isotope labeling with amino acids in cell culture

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