High Pressure Freezing Machine

[custom_headline type=”left” level=”h1″ looks_like=”h2″]High Pressure Freezing Machine HPM 10[/custom_headline][text_output]

The Most Cost Effective, Compact, User Friendly, Cryosectioning System Available.

[/text_output]

[text_output]

  • Four user-adjustable temperature programs
  • Efficient cryogenic design with lowest LN2 consumption
  • Quick set-up and conversion back to room temperature ultramicrotomy
  • Nine liter Dewar fits on table-top, yet provides LN2 for a whole day’s use
  • Compatible with most modern ultramicrotomes
  • Precision microprocessor temperature control from +35°C to -180°C

[/text_output]

[image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2115″ style=”padding-top: 0px;”]
[tabs][tab active=”true”]
[image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2105″ style=”padding-top: 23px;”]
[text_output]

The Golden Standard

With over 100 installations world-wide, and more than 400 scientific publications to its credit, the HPM-010 is not only the pioneer of HP freezing, but the instrument of choice which allows freezing of aqueous samples up to 200µm thickness without visible ice crystal damage and without the use of cryoprotectants.[/text_output]

[text_output]

The High Pressure Freezing Method (HPF)

High pressure freezing is the only method, that allows vitrification of samples up to 1mm3. The HPF method uses LN2 under high pressure (2100 bar). At 2100 bar, water is 1500 times more viscous than at atmospheric pressure, which drastically reduces the crystal growth.[/text_output]

[image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2104″ style=”padding-top: 0px;”]
[text_output]

Let’s compare!

Comparison of chemically fixed and high pressure frozen (using HPM 010) paramecium cells

[/text_output]

[image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2101″ style=”padding-top: 23px;”][text_output]Cross section of cells after chemical fixation

Regular distribution of Ribosomes in the Cytoplasm, granu- lar Glykogen is scarcely visible. Trichocystenbodies (TK) and Trichocystentips (TS) exhibit shrinkage. Surface membranes (M) are crinkled.

All Micrograph Photos: Dr. Heinrich Hohenberg, ETHZ Zurich, Lab. For EM1, CH – 8902 Zurich, Switzerland[/text_output]

[image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2103″ style=”padding-top: 23px;”][text_output]High pressure frozen, freeze substituted Preparation in Cellulose Capillary tubes

Entire Paramecium cell is adequately cryopreserved. Glykogranula (GLY) has high density and occurs in delimited areas, as well as the Ribosomes (RI). Surface membranes are smooth and tight arranged.[/text_output]

[text_output]Comparison of chemically fixed and high pressure frozen (using HPM 010) paramecium cells[/text_output]
[image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2116″ style=”padding-top: 23px;”][text_output]Chemical fixed, room temperature, dehydrated

Trichocyst bodies (TB) is detatched all round from the matrix. Glykogengranula is mixed with the Ribosomes.[/text_output]

[image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2117″ style=”padding-top: 23px;”][text_output]High pressure frozen, freeze substituted Preparation in Cellulose Capillary tubes

No discernible shrinkage of the Trichocysts. Bodies and tips are firmly connected. Glykogengranula (GLY) is delimited from the Ribosome-areas (RI).[/text_output]

[text_output]

More Features…

  • Cryo-fixation of suspensions, monolayer cell cultures and tissues
  • Large base of application know-how available
  • Shortest handling time before freezing
  • Suited for suspension and tissue samples
  • Easy one button operation
  • In situ real time measurement of temperature and pressure
  • Fast 90 second process cycle allows expeditious application
  • Automatic, microprocessor controlled operation for routine work
  • Suited for suspension and tissue samples
  • Compact, sturdy unit with soundproof and vibration-free housing
  • Simple and safe operation due to quick-locking action of specimen holder and clearly arranged operational controls
  • Processing data is recorded on digital display, such as the actual temperature, time and pressure, thus allowing the user to exactly evaluate current operational status (sample quality control)
  • Simple maintenance with removable cover plates and rack system for control units
  • Extensive accessory program

[/text_output]

[/tab][tab]
[text_output]

Dimensions and Weight
Dimensions see diagram below
Weight, approx. 450 kg
Working Data
Working pressure 2300 – 2600 bar
Maximum pressure 2800 bar
Duration of working pressure, at least 500 ms
Cooling time from 0°C to -50°C
(measured between 3 mm copper disc)
10 ms
Specimen Dimensions
Sample size, up to max. of 200μm thickness and 2mm diameter
Connection Data
Voltages, frequencies 3 x 380/220 V, 50 Hz or 3 x 208 V, 60 Hz
Power input, approx. 23kVA
Compressed air (5 bar) G 1/4” (outer thread
LN2 (1 bar excess pressure) G 1/4” (outer thread)
Heating water (rubber hose) Ø 7/14 mm
Operational Data
Hydraulic oil reservoir 40 liters
Hydraulic oil bias pressure 140 – 250 bar
LN2 Dewar (in system) 7 liters
LN2 consumption 10 – 20 liters/hour
Initial system cooling, approx. 15 min.
Max. processing sequence, approx. 40 shots/hour
lsopropyl alcohol reservoir, approx. 0.5 liters

[/text_output][image type=”none” float=”none” info=”none” info_place=”top” info_trigger=”hover” src=”2125″][text_output]Measurements in Millimeters[/text_output]

[/tab][tab][/tab][/tabs]

Scroll to Top