Bruker Corporation (Nasdaq: BRKR), a provider of life science and diagnostics systems and solutions, announced on Monday that it has introduced a USD100 high-fidelity plasma proteomics solution using PreOmics ENRICH and timsTOF HT.
This method enables deep, unbiased plasma proteomics at scale, delivering 99% specificity at 1% false discovery rate (FDR), crucial for large-scale studies in biopharma.
Biognosys is also offering services using its P2 enrichment and Spectronaut 19, allowing identification of up to 9,000 proteins. These offerings include integration with Alamar Bio's ultra-high sensitivity NULISA panels for inflammation and CNS multiplex analysis.
Bruker's glyco-PASEF and timsTOF Ultra 2 enable high-sensitivity glycoproteomics, with a twofold increase in glycopeptide identifications. Enhanced by machine learning, TIMSrescore technology improves peptide identification for post-translational modifications (PTMs) and metaproteomics, ensuring 99.9% specificity at 0.1% FDR.
The company also announced its 4D-Multiomics platform, integrating proteomics, lipidomics and metabolomics insights via ProteoScape, facilitating multi-dimensional analysis for deeper biological understanding.
Amgen updates on data for MariTide
argenx and Zai Lab secure Chinese approval for VYVGART Hytrulo for CIDP
Faron Pharmaceuticals files patent for soluble Clever-1 in autoimmune disease treatment
AstraZeneca's Tezspire achieves positive results in nasal polyps trial
OSE Immunotherapeutics' Lusvertikimab shows promise in ulcerative colitis
Formosa Pharmaceuticals signs licensing agreement with DÁVI Farmaceutica
GlycoMimetics to combine with Crescent Biopharma
Lilly's mirikizumab shows sustained efficacy in IBD
EydisBio receives USD0.5m Phase one SBIR grant from NIH's National Institute on Aging
Redwire partners with Bristol Myers Squibb for space-based drug research
Bruker unveils USD100 deep plasma proteomics solution
Accord Healthcare wins CHMP approval for Stelara biosimilar Imuldosa
Foresee Pharmaceuticals completes linvemastat (FP-020) phase clinical study in Australia
Adicet Bio receives FDA clearance to expand ADI-001 trials to additional autoimmune diseases