Dianthus uHTS measures a 1536-well plate in only 8 minutes, and can be fully automated via an open gRPC framework. Data is delivered in whatever format you need, making it easy to integrate into your existing analysis workflow. No microfluidics minimizes maintenance, letting the instrument run 24/7. Dianthus uHTS does not get in the way, empowering scientists to move faster than ever before.
Drug targets rarely have only one binding site, and with the increasing prevalence of induced proximity modalities that rely on cooperativity to drive ternary complex formation, it is extremely difficult to predict where a molecule will bind your target. Dianthus uHTS does not require prior knowledge of the binding site to collect data, meaning you can identify binders that would be missed during HTRF assays.
Spectral Shift technology only needs one binding partner to be labeled in order to detect an interaction, greatly simplifying assay development. Additionally, measurements happen in-solution, immobilization free, and independent of mass changes upon binding, allowing for more flexibility in assay design.
Spectral Shift technology is already proven as a trusted method for lead validation and optimization, and now it can be used for primary screening as well. Using the same method for primary screening and lead validation negates the need for another round of costly assay development, until you are ready for orthogonal measurements.
Get hours of uninterrupted and unattended operation with a format that’s compatible with any automation solution.
Dianthus uHTS detects a wide range of binding affinities — picomolar to millimolar — so you catch very strong and weak binders.
可在接近天然条件下分析相互作用,特别是在处理具有挑战性的目标。由于测量是在溶液中完成的,因此不必担心对目标结合位点产生负面影响或缺乏对平衡条件的控制。
一点一滴都很重要。节省昂贵的样品和库化合物意味着我们可以做更多的筛选实验或项目
Finding true hits faster is the most important step in making your drug discovery workflow efficient. With Dianthus uHTS, you’ll find hits quickly and move on to hit validation confidently, whether it’s fragment-based or small molecule single-dose screening.
Spectral Shift has already been proven as a trusted method for lead validation. Dianthus uHTS lets you measure in 1536 or 384-well plates, giving you the flexibility you need to validate your hits regardless of library size.
Dianthus uHTS relies on Spectral Shift technology. The process is actually pretty simple: label one binding partner with a fluorophore, then mix a fixed amount of it with a dilution series of the ligand. After excitation at 590nm of the mix, the binding events are detected as shifts of spectra towards either blue or red. The detection of spectral shifts is achieved through dual-wavelength detection at exactly 650nm and 670nm in an isothermal environment — this makes Dianthus uHTS precise enough to detect very subtle shifts, even when taking extremely rapid measurements.
Then the Kd is calculated by plotting the ratios of the fluorescence intensities from the two wavelengths against the ligand concentration.
在发现和验证hits时,如何从较少实验用量中获得您所期望高质量和一致性。Dianthus 1536孔板具有最佳性能和用户体验所需的所有功能:
You’ll also want to use a labeling kit to label your proteins or peptides with fluorophores selected for their sensitivity to binding events — so you get the best results with Spectral Shift.