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TED115126-2026

2026-0931916 - Purchase of an LMD-Thunder System

Ordregiver
Aarhus Universitet
Oplyst værdi / estimat
2.284.227 DKK
Frist
—
Publiceret
18.2.2026
CPV
38000000
Leveringssted (NUTS)
DK042, DNK

Dataposten opdateret . Datakilder, dækning og beregningsmetode.

Tildeling

Vinderlisten dækker bekendtgørelsen. Denne visning har ikke en sikker kobling mellem hver vinder, delkontrakt, værdi og udløbsdato. Se originalen for fordelingen.

Bekendtgørelsens samlede værdi: 2.284.227 DKKKontrakt indgået: 28.1.2026
Triolab A/S
CVR 21481548Oplyst værdi: 2.284.227 DKK

Beløb er offentliggjorte værdier i bekendtgørelser og kan omfatte flere delkontrakter, rammeaftalelofter og estimater. De viser ikke faktisk omsætning eller forbrug. Valutaer summeres hver for sig uden omregning. Manglende beløb er ikke nul. Se datagrundlag og metode.

Beskrivelse
The proposed purchase comprises a Laser Microdissection (LMD7) system integrated with THUNDER 3D fluorescence imaging

Procedure og udbudsmateriale

Oplysninger fra bekendtgørelsen kan dække flere delkontrakter. Listerne nedenfor er separate uddrag; rækkefølgen kobler ikke et kriterium til en beskrivelse eller delkontrakt. Kontrollér krav, vægtning, frister, optioner og eventuelle rettelser i originalmaterialet.

Proceduretype (kildens kode)

  • oth-single

Tildelingskriterier

  • Quality

Beskrivelser af tildelingskriterier

  • The LMD7–THUNDER platform is expected to provide rapid, high-contrast 3D fluorescence imaging of thick and heterogeneous microbiological samples, followed by accurate isolation of selected cells or cell clusters for downstream chemical imaging such as nanoSIMS or Raman microspectroscopy. In this integrated mode, Thunder enhances the visualization of microbial cells in their native structural and chemical environment, improving the accuracy and confidence in identifying cells or regions of interest before laser-assisted isolation or mapping. This 3D imaging capability of the system is critical for investigating complex microbial systems ranging from single cells and mixed microbial consortia to host-associated and environmental microbiomes. The system is the only platform fully interoperable with established spatial chemical imaging workflows enabling methodological compatibility and reproducibility. The instrument should be capable of imaging fluorescently tagged cells and cell clusters, including those containing natural autofluorescence, precisely identifying these and separating them from and within the nearby 3D structures e.g. soil and sediment particles, minerals, plant and animal tissues, electrodes, biofilms etc. Considering the correlative workflows planned and the aim of visualizing microbial cells in their native structural and physical environment it is essential that the LMD instrument is an upright system, has advanced imaging capabilities that allow blur free, clear, high-contrast images even deep within thick samples. The instrument should enable fast multi-colour imaging of 2D and 3D microbial samples (life and dead enrichment cultures, biofilms, cell aggregates, environmental microbial samples: sediment, soil, plant and animal tissue) with improved signal to noise ratio.
Åbn originaludbud

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