Library

Microscoop Enables Subcellular Proteomic Discovery of Stress Granules

A Microscoop® stress granule study identified 1,754 consistently enriched proteins with 96% specificity among the top 50 ranked, including novel SG-associated proteins, uncovering potential therapeutic targets for stress-related diseases.

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Microscoop® Mint Brochure

Syncell Microscoop® integrates cutting-edge microscopy, photo-biotinylation, and mass spectrometry to enable high-resolution, hypothesis-free protein discovery. The platform identifies and isolates proteins from specific cellular structures, such as nuclei, stress granules, and primary cilia, paving the way for advancements in diagnostics, therapeutic development, and disease research.

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Total-sync ultra-content microscopic opto-biotinylation enables high-sensitivity hypothesis-free subcellular protein discovery

High-sensitivity, hypothesis-free spatial proteomics by integrating microscopy-guided photo-biotinylation with LC-MS/MS analysis identifies and maps proteins within compartments such as nuclei, nucleoli, stress granules, and primary cilia.

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Identifying novel mitochondria-lipid droplet interface proteins using microscopy-guided subcellular spatial protein purification

Integrating real-time image segmentation, two-photon photolabeling, and mass spectrometry-based proteomics, Microscoop reveals key regulators of mitochondrial-LD interactions, providing new insights into lipid metabolism and inter-organelle communication.

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Subcellular spatial proteomics by microscopy-guided photo-biotinlaytion reveals novel protein constituents in primary cilia

Microscoop® selectively labels and analyzes primary cilia proteins within subcellular regions of interest, uncovering new ciliary proteins and their interactions.

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Identification of the novel immune synapse-localized proteome for immuno-oncology using Microscoop-induced targeted photo-biotinylation

A new study shows how Microscoop® maps the poorly understood immune synapse-localized proteome more with nanoscale precision, discovering previously uncharacterized proteins and protein-protein interactions, offering new insights into immune synapse biology and potential therapeutic targets in immune-oncology.

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NEW PUBLICATION

PHF19 drives the formation of PRC2 clusters to enhance motility in TNBC cells

Pelzer, Nina et al.
Cell Reports, Volume 44, Issue 10, 116391