Abstract
We present a proximity ligation-based multiplexed protein detection procedure in which several selected proteins can be detected via unique nucleic-acid identifiers and subsequently quantified by real-time PCR. The assay requires a 1-μl sample, has low-femtomolar sensitivity as well as five-log linear range and allows for modular multiplexing without cross-reactivity. The procedure can use a single polyclonal antibody batch for each target protein, simplifying affinity-reagent creation for new biomarker candidates.
Original language | English (US) |
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Pages (from-to) | 327-329 |
Number of pages | 3 |
Journal | Nature Methods |
Volume | 4 |
Issue number | 4 |
DOIs | |
State | Published - Apr 1 2007 |
ASJC Scopus subject areas
- Biotechnology
- Molecular Biology
- Cell Biology