The in situ proximity ligation assay is a powerful technology capable of detecting single protein events such as protein protein interactions (e.g. protein dimerization) and modifications (e.g. protein phosphorylation) in tissue and cell samples prepared for microscopy. Each detected signal is visualized as an individual fluorescent dot, these signals can be quantified (counted) and assigned to a specific subcellular location based on microscopy images. This revolutionary technique enables unprecedented specificity and sensitivity of protein detection and quantification for high performance immunofluorescence and immunohistochemistry applications. Leveraging on Abnova's manufacturing capability and growing collection of 50,000+ antibodies, hundreds of target specific and validated assays are being developed in cells and tissue samples.
Principle of Proximity Ligation Assay
1.
Incubate with target primary antibodies from two different species
2.
Add probes
3.
Hybridize connector oligos
4.
Ligation to form a complete DNA circle
5.
Rolling circle amplification
6.
Add fluorescent probes to reveal protein protein interaction
Huh7 cells were stained with anti-FLT1 rabbit purified polyclonal antibody and anti-CTNNB1 mouse monoclonal antibody. Each red dot represents the detection of protein-protein interaction complex.
HeLa cells were stained with anti-TRAF2 rabbit purified polyclonal antibody and anti-ACTG1 mouse monoclonal antibody. Each red dot represents the detection of protein-protein interaction complex.
HeLa cells were stained with anti-SNCA rabbit purified polyclonal antibody and anti-BAX mouse monoclonal antibody. Each red dot represents the detection of protein-protein interaction complex.