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Microscopes of the light sheet of the Luxendo MuVi SPIM and InVi SPIM series

Bruker

Microscopes of the light sheet of the Luxendo MuVi SPIM and InVi SPIM series

From living embryos to enlightened mouse brains: multi-track and lattice light-sheet shooting

Luxendo’s line of light-leaf microscopes covers tasks from multi-day imaging of living embryos to imaging the enlightened mouse brain and subcellular structures.

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MuVi SPIM illuminates and registers a sample from two opposite sides, supports 360° rotation and is available in LS versions for living and CS for enlightened samples. InVi SPIM Lattice Pro in inverted geometry forms a gauss, Bessel or lattice light sheet using a light modulator and supports SIM, FLIM and FCS. The systems can be equipped with a photo manipulation module and are controlled by LuxControl software.

MuVi SPIM: up to six laser lines 405–785 nm, two-color detection, control 20–37 °C, CO2/O2/N2 and humidity (LS), the volume of the illuminated sample up to 15 × 15 × 20 mm (CS), lenses 4×–20 × InVi SPIM Lattice Pro: 25× 1.1 NA detection lens, 310 nm XY and 530 nm Z in optical lattice mode, 80 frame / s at full frame and up to 500 frame / s on a reduced field.

MuVi SPIM: Multi-Perspective Shooting

  • Simultaneous lighting and detection from two opposite sides without rotating the sample
  • Free axis of rotation and isotropic resolution at one rotation by 90°
  • Simultaneous two-color detection, up to six laser lines 405-785 nm
  • Scanned beam and pivot scanning eliminate stripes and shadows

Living and enlightened patterns

  • LS performance: temperature control 20–37 °C, CO2, O2, N2 and humidity for hours and days
  • CS-performance is compatible with any methods of enlightenment, top-mounting reduces contact with reagents
  • Transition between tasks – rapid change of lenses

InVi SPIM Lattice Pro and Software

  • Inverted geometry and light modulator: gauss, Bessel, static sheet and optical lattice
  • SIM, FLIM and FCS capabilities; up to 500 fps on reduced field
  • LuxControl software: crosslinking hundreds of tiles, merging angles, deconvolution, 3D viewing of multiterabyte data
  • Optional photo manipulation module for all three systems

Lens and field of view

ParameterMuVi SPIM LSMuVi SPIM CSInVi SPIM Lattice Pro
Objects of detection20× 1,0 NA; 16× 0,8 NA20× 1,0 NA; 10× 0,5 NA; 4× 0,28 NANikon CFI Apo 25×W 1.1 NA with correction ring
Lighting lens——Special Optics 28.6×0.7 NA, water immersion
Effective scaling up8–44,4×2,2–40×31.3× or 62.5×
Pixel size146–812 nm163-2925 nm104 or 208 nm
Field of vision299-1664 μm333–5990 μm213 or 426 μm

Resolution and speed

ParameterMuVi SPIM LSMuVi SPIM CSInVi SPIM Lattice Pro
Resolution XY/Z——310 nm/530 nm (optical gratings); 680 nm (Bessel); 750 nm (gauss); 800 nm (static sheet)
Speed——80 fps full frame; up to 500 fps on reduced field

Lighting and detection

ParameterMuVi SPIM LSMuVi SPIM CSInVi SPIM Lattice Pro
Laser linesup to 6, 405–785 nmup to 6, 405–785 nm6
Detectionsimultaneoussimultaneous2 sCMOS cameras, up to 10 filters per camera
Geometry4 axes: 2 lighting + 2 detections, rotation 360°bilateral lighting, single or bilateral detectioninverted

Samples and environment

ParameterMuVi SPIM LSMuVi SPIM CSInVi SPIM Lattice Pro
Environmental control20–37 °C; CO2, O2, N2; humidity—20–37 °C; CO2, O2, N2; humidity
Samples.living organisms and embryosorganoids to the enlightened mouse brain; scanned volume 15 × 15 × 20 mmSingle cells, 3D cultures, small organisms
Installation—hook, plate, pin, cuvette; node 3D-movement / rotation from above—

Software

ParameterMuVi SPIM LSMuVi SPIM CSInVi SPIM Lattice Pro
SoftwareLuxControl: collection, viewing, processing; TIFF, HDF5, IMS formats; script management