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Merck

Proximal Ligation Assay (PLA) on Lung Tissue and Cultured Macrophages to Demonstrate Protein-protein Interaction.

Bio-protocol (2017-11-25)
Roberto Mendez, Santanu Banerjee
RESUMEN

In this protocol, we describe proximal ligation assay (PLA), an antibody-based detection method for protein-protein interaction. This method relies on specific binding of individual primary antibodies to the two putative interacting proteins. The primary antibodies need to have different hosts. The secondary antibodies against the two hosts have complementary oligonucleotide moieties attached to them. If the two antigens are in close proximity (presumably interacting with each other), the complementary oligonucleotides can anneal and fluorescent nucleotides can be incorporated in a single DNA polymerization step. Under a microscope, these reactions appear as punctate fluorescent spots, indicating successful PLA reaction and suggesting protein-protein interaction between the two antigens.

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Reactivos rojos para detección in situ Duolink®
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Duolink® In Situ Detection Reagents Orange
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Duolink® In Situ Detection Reagents FarRed
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Duolink® In Situ Detection Reagents Green
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Duolink® In Situ Wash Buffers, Fluorescence
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Duolink® In Situ Mounting Medium with DAPI
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Duolink® In Situ Detection Reagents Brightfield
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Duolink® In Situ Probemaker PLUS
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Duolink® In Situ Probemaker MINUS
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Duolink® flowPLA Detection Kit - FarRed, Duolink® PLA kit for Flow Cytometry with FarRed Detection
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Duolink® flowPLA Detection Kit - Red, DUOLINK® : PLA kit for Flow Cytometry with Red Detection
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Duolink® flowPLA Detection Kit - Green, Duolink® PLA kit for Flow Cytometry with Green Detection
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Duolink® In Situ Wash Buffer, Brightfield
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Duolink® In Situ Microplate Nuclear Stain, Anti-Fade
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Duolink® In Situ Microplate Heat Transfer Block
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Duolink® flowPLA Detection Kit - Orange, Duolink® PLA kit for Flow Cytometry with Orange Detection