bioRxiv / medRxiv
open access
Coupling cell growth to protein secretion enables pooled screening at single-cell resolution in bioreactors
Preserving the genotype-phenotype linkage is critical in high-throughput screens exploring large parameter spaces. Screening pooled libraries for recombinant protein secretion is therefore particularly difficult, since protein diffusion into the medium disrupts this linkage. Existing methods impose
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
- Large-scale statistical dissection of sequence-derived biochemical features distinguishing soluble and insoluble proteins.#265209
- Large-Scale Statistical Dissection of Sequence-Derived Biochemical Features Distinguishing Soluble and Insoluble Proteins#170850
- EMERALD-UI: an interactive web application to unveil novel protein biology hidden in the alternative alignment space.#224798
- Condensin loop extrusion properties, roadblocks, and role in homology search during recombination in S. cerevisiae.#159881
- Protocol for the in vivo quantification of mitochondria-associated ER membranes in Caenorhabditis elegans.#251158
Record · ID 1361623
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