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compasstm ‘dataanalysis’ software  (Bruker Corporation)


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    Structured Review

    Bruker Corporation compasstm ‘dataanalysis’ software
    Compasstm ‘Dataanalysis’ Software, supplied by Bruker Corporation, 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/compasstm+dataanalysis+software/compasstm++dataanalysis%E2%80%99+software/pmc08143643-195-39-43
    Average 90 stars, based on 1 article reviews
    compasstm ‘dataanalysis’ software - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Software:

    Article Title: Accurate MS-based Rab10 Phosphorylation Stoichiometry Determination as Readout for LRRK2 Activity in Parkinson's Disease
    Article Snippet: .. Proteins were eluted with a gradient of 20-80% buffer B in 20 min. After each gradient, the column was washed with 95% buffer B for one minute and 20% buffer B for 3 min. Data were processed using the CompassTM `DataAnalysis` software from Bruker Daltonik, deconvoluted with `MaximumEntropy` and an instrument resolving power of 10,000. ..

    Article Title: Accurate MS-based Rab10 Phosphorylation Stoichiometry Determination as Readout for LRRK2 Activity in Parkinson's Disease
    Article Snippet: An Agilent 1100 HPLC system was coupled online with the mass spectrometer (microTOF, Bruker Daltonik) and masses were recorded from 800–3000 m / z . Proteins were separated with a binary buffer system of buffer A (0.05% TFA in H 2 O, pH 2.0) and buffer B (0.05% TFA in can, pH 2.0) at a flow rate of 250 nl/min. .. Proteins were eluted with a gradient of 20–80% buffer B in 20 min. After each gradient, the column was washed with 95% buffer B for 1 min and 20% buffer B for 3 min. Data were processed using the CompassTM ‘DataAnalysis’ software from Bruker Daltonik, deconvoluted with ‘MaximumEntropy’ and an instrument resolving power of 10,000. ..

    Article Title: Accurate MS-based Rab10 phosphorylation stoichiometry determination as readout for LRRK2 activity in Parkinson’s disease
    Article Snippet: .. Proteins were eluted with a gradient of 20-80% buffer B in 20 min. After each gradient, the column was washed with 95% buffer B for one minute and 20% buffer B for 3 min. Data were processed using the CompassTM ‘DataAnalysis’ software from Bruker Daltonik, deconvoluted with ‘MaximumEntropy’ and an instrument resolving power of 10,000. ..



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