Bekendtgørelse om frivillig forudgående gennemsigtighed · 22. december 2025
BD FACSDiscover A8 Cell Analyser with BD CellView Image Technology
Danmarks Tekniske Universitet - DTU offentliggjorde 22. december 2025 en bekendtgørelse om frivillig forudgående gennemsigtighed om »BD FACSDiscover A8 Cell Analyser with BD CellView Image Technology«.
- Type
- Bekendtgørelse om frivillig forudgående gennemsigtighed
- Ordregiver
- Danmarks Tekniske Universitet - DTU
- By
- Kgs. Lyngby
- Offentliggjort
- 22. december 2025
- Kontrakttype
- Varer
- Procedure
- Udbud med forhandling uden forudgående offentliggørelse
- CPV-koder
- 38433000, 38000000, 38400000, 38430000
- Udførelsessted (NUTS)
- DK012
- TED-nummer
- 855106-2025
Beskrivelse fra ordregiveren
DTU will like to buy a BD FACSDiscover A8 5 Laser 78 detectors from BD Biosciences. The instrument will include the following : • Forward Scatter: Label-free brightfield imaging channel that measures light scattered at small forward angles by the cell as it passes through the laser interrogation point. • SSC Imaging: Label-free imaging channel measuring light scattered at 90° perpendicular to the laser path, capturing internal cellular complexity. • Lightloss Imaging: Measures the total photons lost from the laser beam due to both scattering and absorption by the cell, allowing Label-free brightfield imaging morphological assessment. • Channel 1: Fluorescence imaging (530/30nm range) • Channel 2: Fluorescence imaging (600/60nm range) • Channel 3: Fluorescence imaging (788/225nm range) These imaging channels enable spatial analysis of protein localisation, cellular interactions, and morphological characteristics that remain invisible to traditional flow cytometry. The system generates quantitative image parameters including: • Area and Perimeter measurements for size discrimination • Aspect Ratio and Eccentricity for shape analysis • Diffusivity for texture characterisation • Correlation and Distance for multi-channel co-localisation • Radial Moment for signal distribution analysis. Applications enabled by this technology include: • Identification of subcellular protein localisation (nuclear vs cytoplasmic) • Detection of cell-cell interactions and immunological synapses • Discrimination of budding yeast cells and cell aggregates • Analysis of phagocytosis and particle uptake • Label-free morphological study for downstream sorting. Complementing the imaging capabilities, the instrument should hold a technology for full-spectrum flow cytometry. This system features: • 5 laser configuration: 349 nm (UV), 405 nm (Violet), 488 nm (Blue), 561 nm (Yellow-Green), 637 nm (Red) • 78 fluorescence detectors capturing complete emission spectra • 8 scatter and imaging detectors • System-aware spectral unmixing algorithms that adapt to instrument performance in real-time • Capability for 40+ parameter experiments with optimal resolution and sensitivity Complementing the imaging capabilities, the instruments should include a technology for full-spectrum flow cytometry. This system features: • 5 laser configuration: 349 nm (UV), 405 nm (Violet), 488 nm (Blue), 561 nm (Yellow-Green), 637 nm (Red) • 78 fluorescence detectors capturing complete emission spectra • 8 scatter and imaging detectors • System-aware spectral unmixing algorithms that adapt to instrument performance in real-time • Capability for 40+ parameter experiments with optimal resolution and sensitivity
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Kilde
Bekendtgørelsen er offentliggjort i TED (nr. 855106-2025). Teksten er ordregiverens egen. Udbudsmaterialet og eventuelle rettelser findes hos ordregiveren eller i TED. Genbrug med kildeangivelse (Kommissionens afgørelse 2011/833/EU).