2003
DOI: 10.1002/jms.505
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Direct tissue analysis using matrix‐assisted laser desorption/ionization mass spectrometry: practical aspects of sample preparation

Abstract: Practical guidelines for the preparation of tissue sections for direct analysis by matrix-assisted laser desorption/ionization (MALDI) mass spectrometry are presented. Techniques for proper sample handling including tissue storage, sectioning and mounting are described. Emphasis is placed on optimizing matrix parameters such as the type of matrix molecule used, matrix concentration, and solvent composition. Several different techniques for matrix application are illustrated. Optimal instrument parameters and t… Show more

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Cited by 584 publications
(696 citation statements)
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References 16 publications
(33 reference statements)
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“…For stigmatic MALDI experiments, tissues were briefly washed in cold 70% ethanol and dried at room temperature before matrix deposition. 43 Matrix Deposition. ME-SIMS matrix was applied using electrospray deposition as described previously.…”
Section: Methodsmentioning
confidence: 99%
“…For stigmatic MALDI experiments, tissues were briefly washed in cold 70% ethanol and dried at room temperature before matrix deposition. 43 Matrix Deposition. ME-SIMS matrix was applied using electrospray deposition as described previously.…”
Section: Methodsmentioning
confidence: 99%
“…Previous studies have highlighted the need to consider sample preparation as a critical component in developing MALDI IMS applications [4,8,39]. However, in spite of the effort to exert control over environmental factors affecting matrix applications, instrument variation during the course of data collection, and inherent cellular heterogeneity within the samples themselves, there is inevitably some contribution of each of these effects to the image.…”
Section: Processing Of Imaging Mass Spectrometry Datamentioning
confidence: 99%
“…After washing, the tissue sections were allowed to dry for 30 min after which the matrix was°applied° [41]°using°a°TLC°sprayer°[42,°43]°(30 mg/mL of 2,5-dihydroxybenzoic acid in 50:50 ethanol/ water and 0.1% trifluoroacetic acid). The sample was then covered with a 3 nm layer of gold using a plasma sputter coater (Quorum Technologies, Newhaven, United Kingdom).…”
Section: Tissue Sectionsmentioning
confidence: 99%