2015
DOI: 10.1039/c5ay02252e
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Analysis of latex protein content by liquid chromatography coupled with tandem mass spectrometry (HPLC/MS/MS)

Abstract: Quantification of raw latex and latex glove proteins was carried out by liquid chromatography coupled with tandem mass spectrometry.

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Cited by 2 publications
(3 citation statements)
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“…Method LOD and LOQ values (the lowest amount of AA detectable in the sample) listed in Supporting Information Table S1 are concentrations corresponding to the average blank signal plus three (LOD) and ten (LOQ) SDs of the blank . Method sensitivity was 10–100 times higher than the GC–MS methods used for the protein binders identification and it was also superior to the LC–MS method described in our previous study where C18 column was used . LOD and LOQ values listed in Supporting Information Table S1 were comparable with the sensitivity of similar method, where a ZIC–HILIC column was used .…”
Section: Resultsmentioning
confidence: 71%
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“…Method LOD and LOQ values (the lowest amount of AA detectable in the sample) listed in Supporting Information Table S1 are concentrations corresponding to the average blank signal plus three (LOD) and ten (LOQ) SDs of the blank . Method sensitivity was 10–100 times higher than the GC–MS methods used for the protein binders identification and it was also superior to the LC–MS method described in our previous study where C18 column was used . LOD and LOQ values listed in Supporting Information Table S1 were comparable with the sensitivity of similar method, where a ZIC–HILIC column was used .…”
Section: Resultsmentioning
confidence: 71%
“…AAs were quantified in the SRM mode (Supporting Information Fig. S2) as described in our previous study . Method LOD and LOQ values (the lowest amount of AA detectable in the sample) listed in Supporting Information Table S1 are concentrations corresponding to the average blank signal plus three (LOD) and ten (LOQ) SDs of the blank .…”
Section: Resultsmentioning
confidence: 99%
“…BSA was used as the model NRL proteins. [33][34][35][36] Protein detection was conducted using the ePAD without an ex situ sample pretreatment step. A protein sample was reacted with the optimum 600 μg mL −1 Cu(II) at the reaction chamber for 1 min before the remaining Cu(II) was electrochemically measured.…”
Section: Electrochemical Detection Of Proteinmentioning
confidence: 99%