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Scott D. Tanner

Researcher at University of Toronto

Publications -  91
Citations -  8265

Scott D. Tanner is an academic researcher from University of Toronto. The author has contributed to research in topics: Inductively coupled plasma mass spectrometry & Mass spectrometry. The author has an hindex of 39, co-authored 91 publications receiving 7651 citations. Previous affiliations of Scott D. Tanner include University Health Network & Cameron International.

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A sensitive and quantitative element-tagged immunoassay with ICPMS detection.

TL;DR: These immunoassays are directly coupled with an inductively coupled plasma mass spectrometer (ICPMS) to quantify the elemental component of the reacted tagged antibodies to detect proteins of interest using specific element-tagged antibodies.
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A dynamic reaction cell for inductively coupled plasma mass spectrometry (ICP-DRC-MS). Part III. Optimization and analytical performance

TL;DR: The dynamic reaction cell (DRC) as mentioned in this paper is a quadrupole which may be pressurized with a reactive gas in order to suppress plasma-based isobaric interferences for trace elemental analysis.
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Characterization of ionization and matrix suppression in inductively coupled ‘cold’ plasma mass spectrometry

TL;DR: A parametric study of plasma power and central gas flow was carried out to study the transition from normal analytical conditions to cooler plasma conditions using an inductively coupled plasma mass spectrometer having a balanced load coil as mentioned in this paper.
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Detection of ultratrace phosphorus and sulfur by quadrupole ICPMS with dynamic reaction cell

TL;DR: A method of detection of ultratrace phosphorus and sulfur that uses reaction with O2 in a dynamic reaction cell (DRC) to oxidize S+ and P+ to allow their detection as SO+ and PO+ is described, reducing the effect of polyatomic isobaric interferences.
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Multiple cellular antigen detection by ICP-MS

TL;DR: A novel application of ICP-MS-linked metal-tagged immunophenotyping which has great potential for highly multiplexed proteomic analysis and is already apparent that more than four antigens could be accurately detected simultaneously using the I CP-MS instrument.