International audienceWe report three derivatization strategies for CE analysis with LIF detection (CE‐LIF) of two synthetic peptides mimicking the wild and mutated fragments of interest for the diagnosis of familial transthyretin amyloidosis. The precapillary derivatization of the peptides with three optical tags, 5‐carboxytetramethylrhodamin succinimidyl ester (TAMRA‐SE), naphtalene‐2,3‐dicarboxyaldehyde (NDA), and 3‐(2‐furoyl)quinoline‐2‐carboxyaldehyde (FQ) has been investigated by CE‐LIF detection and MS. Results provide evidence that high reaction yields have been reached whereas the multitagging phenomenon has occurred for both NDA and TAMRA‐SE labeling procedures. The derivatization and electrokinetic separation of a mixture of the ...
ac.jp. BACKGROUND: Mass spectrometric analyses are valuable for detection of transthyretin (TTR) var...
The analysis of low abundant proteins in biological fluids by capillary electrophoresis (CE) is part...
Immunoglobulin light chain (LC) amyloidosis (AL) is caused by deposition of clonal LCs produced by a...
International audienceWe report three derivatization strategies for CE analysis with LIF detection (...
International audienceLabelling and detection of a synthetic peptide (PN) mimicking a tryptic fragme...
The purpose of our work was the development of new analytical methodologies to measure the benefit o...
Ces travaux de recherche s’intéressent à la conception de nouvelles méthodologies analytiques destin...
La polyneuropathie amyloïde familiale à transthyrétine (FAP-TTR) est une maladie rare héréditaire à ...
AbstractIn our continuing efforts to develop mass spectrometry-based methods for transthyretin (TTR)...
Development of a quantification method based on isotopic variants of O-methyl isourea (OMIU) in conj...
Transthyretin (TTR) amyloidosis is a disease that appears in three variants. One variant affects the...
AbstractVariant forms of the plasma protein transthyretin (TTR) are associated with the most frequen...
Proteomics is becoming the de facto gold standard for identifying amyloid proteins and is now used r...
Transthyretin familial amyloid polyneuropathy (TTR-FAP) is a hereditary rare disease with an autosom...
In this paper, an on-line immunoaffinity solid-phase extraction capillary electrophoresis mass spect...
ac.jp. BACKGROUND: Mass spectrometric analyses are valuable for detection of transthyretin (TTR) var...
The analysis of low abundant proteins in biological fluids by capillary electrophoresis (CE) is part...
Immunoglobulin light chain (LC) amyloidosis (AL) is caused by deposition of clonal LCs produced by a...
International audienceWe report three derivatization strategies for CE analysis with LIF detection (...
International audienceLabelling and detection of a synthetic peptide (PN) mimicking a tryptic fragme...
The purpose of our work was the development of new analytical methodologies to measure the benefit o...
Ces travaux de recherche s’intéressent à la conception de nouvelles méthodologies analytiques destin...
La polyneuropathie amyloïde familiale à transthyrétine (FAP-TTR) est une maladie rare héréditaire à ...
AbstractIn our continuing efforts to develop mass spectrometry-based methods for transthyretin (TTR)...
Development of a quantification method based on isotopic variants of O-methyl isourea (OMIU) in conj...
Transthyretin (TTR) amyloidosis is a disease that appears in three variants. One variant affects the...
AbstractVariant forms of the plasma protein transthyretin (TTR) are associated with the most frequen...
Proteomics is becoming the de facto gold standard for identifying amyloid proteins and is now used r...
Transthyretin familial amyloid polyneuropathy (TTR-FAP) is a hereditary rare disease with an autosom...
In this paper, an on-line immunoaffinity solid-phase extraction capillary electrophoresis mass spect...
ac.jp. BACKGROUND: Mass spectrometric analyses are valuable for detection of transthyretin (TTR) var...
The analysis of low abundant proteins in biological fluids by capillary electrophoresis (CE) is part...
Immunoglobulin light chain (LC) amyloidosis (AL) is caused by deposition of clonal LCs produced by a...