eScholarship
metadata only
Epi-illumination SPIM for volumetric imaging with high spatial-temporal resolution
We designed an epi-illumination SPIM system that uses a single objective and has a sample interface identical to that of an inverted fluorescence microscope with no additional reflection elements. It achieves subcellular resolution and single-molecule sensitivity, and is compatible with common biolo
Conceptio Open Archive
Analyze & explore related research in Conceptio
Connect this record directly into your research workflow or AI agent. Explore citations across open repositories, query full text, and export structured proof bundles.
This document is indexed with metadata only: full text is not available in the archive for this record. Open the official source ↗
Related documents
- Fluorescence-lifetime encoding for scalable single-protein-resolution imaging#669764
- Advances, Challenges, and Opportunities in Electrochemiluminescence Bioimaging.#415353
- Multiplexed Nanophotonic Sensor Arrays for Time-resolved Biomolecular Analysis#155935
- Multiplexed nanophotonic sensor arrays for time-resolved biomolecular analysis.#125470
- From hotspots to hotspaces: Cascaded photonic-plasmonic coupling for SERS-based deep profiling of whole small extracellular vesicles.#182363
Record · ID 1089996
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Retrieved via Conceptio: every document is proof-bundled with source, license, and retrieval metadata.
Bring this data into your agent: Connect via MCP or API · 20 free credits to start · no card required
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive
Read the Docs → · View CLI source on GitHub · Conceptio Open Knowledge Archive