Subcellular localization, protein-protein and protein-nucleic acid interaction studies
A next-generation protein interaction screening technology based on HTRF. Provides real experimental validation with dramatically lower cost than conventional methods like Co-IP. Fast, quantitative, and ideal for large-scale screening in plant research.
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Visualize protein localization in plant cells using fluorescent protein tagging. Supports confocal microscopy for precise cellular compartment identification.
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Screen protein-protein interactions using yeast two-hybrid libraries. Identify new interaction partners for your target proteins.
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Detect protein complexes in plant tissues or cell extracts, allowing confirmation of in vivo interactions.
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Identify interacting proteins using immunoprecipitation coupled with mass spectrometry for comprehensive interactome analysis.
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Visualize protein-protein interactions in living plant cells using split fluorescent proteins for spatial interaction analysis.
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Electrophoretic mobility shift assay to detect protein-DNA/RNA interactions. Analyze transcription factor binding specificity and affinity.
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Screen transcription factor binding to DNA elements using yeast one-hybrid libraries. Ideal for promoter analysis and regulatory network studies.
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Measure promoter activity and transcriptional regulation using two luciferases. Useful for validating regulatory elements in plant systems.
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Detect protein-protein or protein-DNA interactions via split luciferase complementation. Monitor real-time interactions in living cells.
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Plant gene editing has become a powerful approach for studying gene function and improving crop traits.
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