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Decon Laboratories decon-2ls
Decon 2ls, supplied by Decon Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/decon-2ls/decon+2ls/pm24059326__ja406860e_si_001-92-14-1
Average 90 stars, based on 1 article reviews
decon-2ls - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Comparison:

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: 29 Quantitative Comparison of Differences in Phosphopeptide Levels Several programs developed in-house, i.e., Decon-2LS”, 30 “MultiAlign”, 31 and “DAnTE”, 32 (available at http://ncrr.pnl.gov/software ) were employed to process mass spectral data and generate matrices for quantitative comparisons of the phosphoproteomes from bleomycin-treated cells expressing either WT-PP5 or catalytically inactive PP5(H304Q).

Article Title: Structural evidence for a two-regime photobleaching mechanism in a reversibly switchable fluorescent protein.
Article Snippet: For the evaluations of the ratio between oxidized and non-oxidized forms, the 6 raw files were deconvoluted and aligned using the Decon-2ls and MultiAlign software suite.

Article Title: Structural evidence for a two-regime photobleaching mechanism in a reversibly switchable fluorescent protein.
Article Snippet: The Decon-2LS and Multi-Align softwares used for MS data processing were provided by the W. R. Wiley Environmental Molecular Science Laboratory, a national scientific user facility sponsored by the US Department of Energy’s Office of Biological and Environmental Research, located at PNNL. (OMICS.PNL.GOV).

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: Peptide mass and retention time “features” were extracted from de-isotoped datasets using Decon-2LS, and phosphopeptides with FDR ≤ 5% were used to construct an accurate mass and time tag (AMT) database.

Article Title: Influence of mass resolution on species matching in accurate mass and retention time (AMT) tag proteomics experiments.
Article Snippet: *Correspo toire d’E Martyrs, E-mail: ch Contract/ tract/gra Contract/ pôle, and Diverse mass spectrometric instruments have been used to provide data for accurate mass and retention time (AMT) tag proteomics analyses, including ion trap, quadrupole time-of-flight, and Fourier transform mass spectrometry (FTMS).. An important attribute of these instruments, beside mass accuracy, is their spectral resolution.. In fact, the ability to separate peakswith closem/z values is likely to play amajor role in enabling species identification andmatching in analyses of very complex proteomics samples.

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: Several programs developed in-house, i.e., Decon-2LS”, 30 “MultiAlign”, 31 and “DAnTE”, 32 (available at http://ncrr.pnl.gov/software ) were employed to process mass spectral data and generate matrices for quantitative comparisons of the phosphoproteomes from bleomycin-treated cells expressing either WT-PP5 or catalytically inactive PP5(H304Q).

Phospho-proteomics:

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: 29 Quantitative Comparison of Differences in Phosphopeptide Levels Several programs developed in-house, i.e., Decon-2LS”, 30 “MultiAlign”, 31 and “DAnTE”, 32 (available at http://ncrr.pnl.gov/software ) were employed to process mass spectral data and generate matrices for quantitative comparisons of the phosphoproteomes from bleomycin-treated cells expressing either WT-PP5 or catalytically inactive PP5(H304Q).

Article Title: Structural evidence for a two-regime photobleaching mechanism in a reversibly switchable fluorescent protein.
Article Snippet: For the evaluations of the ratio between oxidized and non-oxidized forms, the 6 raw files were deconvoluted and aligned using the Decon-2ls and MultiAlign software suite.

Article Title: Structural evidence for a two-regime photobleaching mechanism in a reversibly switchable fluorescent protein.
Article Snippet: The Decon-2LS and Multi-Align softwares used for MS data processing were provided by the W. R. Wiley Environmental Molecular Science Laboratory, a national scientific user facility sponsored by the US Department of Energy’s Office of Biological and Environmental Research, located at PNNL. (OMICS.PNL.GOV).

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: Peptide mass and retention time “features” were extracted from de-isotoped datasets using Decon-2LS, and phosphopeptides with FDR ≤ 5% were used to construct an accurate mass and time tag (AMT) database.

Article Title: Influence of mass resolution on species matching in accurate mass and retention time (AMT) tag proteomics experiments.
Article Snippet: *Correspo toire d’E Martyrs, E-mail: ch Contract/ tract/gra Contract/ pôle, and Diverse mass spectrometric instruments have been used to provide data for accurate mass and retention time (AMT) tag proteomics analyses, including ion trap, quadrupole time-of-flight, and Fourier transform mass spectrometry (FTMS).. An important attribute of these instruments, beside mass accuracy, is their spectral resolution.. In fact, the ability to separate peakswith closem/z values is likely to play amajor role in enabling species identification andmatching in analyses of very complex proteomics samples.

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: Several programs developed in-house, i.e., Decon-2LS”, 30 “MultiAlign”, 31 and “DAnTE”, 32 (available at http://ncrr.pnl.gov/software ) were employed to process mass spectral data and generate matrices for quantitative comparisons of the phosphoproteomes from bleomycin-treated cells expressing either WT-PP5 or catalytically inactive PP5(H304Q).

Expressing:

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: 29 Quantitative Comparison of Differences in Phosphopeptide Levels Several programs developed in-house, i.e., Decon-2LS”, 30 “MultiAlign”, 31 and “DAnTE”, 32 (available at http://ncrr.pnl.gov/software ) were employed to process mass spectral data and generate matrices for quantitative comparisons of the phosphoproteomes from bleomycin-treated cells expressing either WT-PP5 or catalytically inactive PP5(H304Q).

Article Title: Structural evidence for a two-regime photobleaching mechanism in a reversibly switchable fluorescent protein.
Article Snippet: For the evaluations of the ratio between oxidized and non-oxidized forms, the 6 raw files were deconvoluted and aligned using the Decon-2ls and MultiAlign software suite.

Article Title: Structural evidence for a two-regime photobleaching mechanism in a reversibly switchable fluorescent protein.
Article Snippet: The Decon-2LS and Multi-Align softwares used for MS data processing were provided by the W. R. Wiley Environmental Molecular Science Laboratory, a national scientific user facility sponsored by the US Department of Energy’s Office of Biological and Environmental Research, located at PNNL. (OMICS.PNL.GOV).

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: Peptide mass and retention time “features” were extracted from de-isotoped datasets using Decon-2LS, and phosphopeptides with FDR ≤ 5% were used to construct an accurate mass and time tag (AMT) database.

Article Title: Influence of mass resolution on species matching in accurate mass and retention time (AMT) tag proteomics experiments.
Article Snippet: *Correspo toire d’E Martyrs, E-mail: ch Contract/ tract/gra Contract/ pôle, and Diverse mass spectrometric instruments have been used to provide data for accurate mass and retention time (AMT) tag proteomics analyses, including ion trap, quadrupole time-of-flight, and Fourier transform mass spectrometry (FTMS).. An important attribute of these instruments, beside mass accuracy, is their spectral resolution.. In fact, the ability to separate peakswith closem/z values is likely to play amajor role in enabling species identification andmatching in analyses of very complex proteomics samples.

Article Title: Novel Ser/Thr Protein Phosphatase 5 (PP5) Regulated Targets during DNA Damage Identified by Proteomics Analysis
Article Snippet: Several programs developed in-house, i.e., Decon-2LS”, 30 “MultiAlign”, 31 and “DAnTE”, 32 (available at http://ncrr.pnl.gov/software ) were employed to process mass spectral data and generate matrices for quantitative comparisons of the phosphoproteomes from bleomycin-treated cells expressing either WT-PP5 or catalytically inactive PP5(H304Q).



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