User Tools

Site Tools


blaze

Location: [Oeiras] Room 0B10
Manufacturer: Miltenyi
Model: UltraMicroscope Blaze Lightsheet
Nickname: Blaze
Software: ImSpector
Year: 2024
SN:
 
Miltenyi UltraMicroscope Blaze Quality Control
Miltenyi UltraMicroscope Blaze Usage Statistics

Microscope overview

The UltraMicroscope Blaze is a lightsheet for large cleared samples system with dual sided illumination, capable of using three beams per side. This allows for uniform imaging with minimal shadows (in good sample clearing conditions). Equipped with three objectives (1.1x, 4x and 12x) and internal magnifications of 0.6x, 1x, 1.66x and 2.5x, this system is capable of going from whole organs to single cell level. There are 4 laser lines in the Blaze, 488, 561, 640 and 785 nm, and with the capability of combining these with any of the installed filters, the system is capable of mix-matching for markers such as Propidium Iodide.

Usage conditions

The default configuration for the UltraMicroscope Blaze is for the Refractive Index of DBE (iDisco protocol) at RI = 1.56. Any use where another immersion media is necessary, the system will need realignment, and possibly undergo objective dipping-cap changes (below RI = 1.49). The time taken to do these alignments (DBE to immersion media, immersion media to DBE) can vary between 1-3 hours, and will be charged to the user in question.

Laser Lines

Wavelength (nm) Fluorophores Penetration capability
488 E.g: GFP, TRITC, AL488 Less penetration
561 E.g: mCherry, RFP, AL594 Good penetration
640 E.g: Cy5, TexasRed, AL647 High penetration
785 E.g: Atto740, Atto790 Highest penetration

Fluorescence filters

Position Filterset Emission (nm)
1 488 525/50
2 561 595/40
3 640 680/30
4 785 LP 805
5 Empty -
6 Empty -
7 Empty -

Objectives

Magnification Dipping caps RI range NA WD per dipping cap (mm) Maximum Theoretical Resolution (um)
1.1x 1.33-1.49 / 1.50-1.57 0.1 16 / 17.6 4.8
4x 1.33-1.41 / 1.42-1.48 / 1.49-1.57 0.35 >=15 / >=15 / >=15 1.3
12x 1.33-1.41 / 1.42-1.48 / 1.49-1.57 0.55 8.5 / 10.9 / 10 0.5

Objectives + Zoom

Objective Zoom Final Magnification Field of view (mm)
1.1x 0.6x 0.66x
1.1x 1x 1.1x
1.1x 1.66x ~1.83x
1.1x 2.5x 2.75x
4x 0.6x 2.4x
4x 1x 4x
4x 1.66x 6.64x
4x 2.5x 10x
12x 0.6x 7.2x
12x 1x 12x
12x 1.66x 19.92x
12x 2.5x 30x

Camera

Model Frame Size Pixel Size (µm) Quantum Efficiency
PCO Edge 5.5 sCMOS 2048 × 2048 6.5 x 6.5 60%

Microscope Turn On Procedure

  • Turn on the power bar on top of the microscope's computer, under the table.

Microscope Turn Off Procedure

  • With the software still open, pull out the cuvette drawer.
  • Wait for the drawer to move all the way down.
  • Remove any used cuvette.
  • Press the drawer button, but do not push the drawer in.
  • In software, change to 12x objective and lower the objectives all the way.
  • Turn off the power bar on top of the microscope's computer, under the table.
  • Close the cuvette drawer and software.

Back to the Equipment page

blaze.txt · Last modified: 2025/02/03 12:51 by bioimaging