Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Fragmentation matters and one type is not always enough. Product ion spectra quality can determine whether you make ground-breaking discoveries or get no results at all. The flexibility to use multiple ion-ion interaction techniques can be the experiment breakpoint.
For increased identification and characterization of molecules, many experiment types can benefit from alternate fragmentation and ion-ion interactions. Applications, including glycoproteomics, lipidomics, metabolomics, and biologics characterization, benefit from the use of multiple fragmentation and ion manipulation techniques.
Thermo Fisher Scientific offers a wide array of fragmentation technologies for optimum coverage to produce high confidence identifications. Achieve your scientific goals with innovative instrumentation that maintains ease-of-use with pre-built template methods.
Discover how alternate fragmentation/ion-ion interaction solves multiple analytical problems, from glycoproteomics to the most complex biologics.
Collisional-based fragmentation techniques are the most common. In the highlighted systems, CID occurs in the high-pressure cell of the dual cell linear ion trap assembly. HCD typically occurs in the ion routing multiple. Common applications include proteomics, metabolomics, lipidomics, oligonucleotides, and beyond.
ETD provides orthogonal fragmentation to collision-based methods and is gentler, thus good for the study of labile compounds. Radical fluoranthene transfers its electron to a cation precursor to induce the reaction. Common applications include glycoproteomics, particularly o-linked and heavily glycosylated peptides, and top-down proteomics.
PTCR is an ion-ion interaction that reduced the average charge of the parent cations, shifting the resulting spectra to higher m/z, simplifying the complex ion populations. This method can be used to make extremely heterogenous ion populations deconvolutable. Common applications include biopharma, including fusion proteins, ADCs, and proteomics, including PTM and top-down proteomics.
UVPD energizes ions via absorption of high-energy photons, which allows for access to different dissociation pathways than most techniques. At 213 nm, UVPD can produce a, b, c and x, y, z fragment types for proteins/peptides, and allow for unique structural fragments for small molecules and lipids. Common applications are proteins, metabolomics, and lipidomics.
For Research Use Only. Not for use in diagnostic procedures.