Revision as of 11:00, 1 October 2020

Feedback to this page: click here

Plunge Freezer

Leica EM GP2

Plunge freezing is a cryo-fixation method used to preserve samples in their most native state prior to cryo-electron microscopy. The EM GP2 plunge freezes fluid or extremely thin samples spread on an electron microscopy grid into liquid ethane after removing excess fluid by automatic blotting. Prior to freezing, the sample is maintained in a temperature and humidity controlled environmental chamber, adjustable between +4°C and +60°C and room humidity to 99 %.

The main steps of this technique proceed as follows:
1. The sample is spread into a thin film across an EM grid
2. The liquid droplet is then blotted with filter paper until only a very thin film of fluid remains
3. The grid is then rapidly plunged into a cryogen (usually liquid ethane)
4. The grid is afterwards stored in a grid box submerged in liquid nitrogen until finally loaded into the cryo-electron microscope for imaging

Operating manual: File:Leica EM GP2 Operating manual.pdf
Risk Assessment: File:Risk assessment - EM GP2 Plunge Freezer.pdf

For further information on the equipment usage or training contact mktracy@dtu.dk [1].

High Pressure Freezer

Leica EM ICE (COMING SOON)

High pressure freezing is key for the study of intricate changes in fine structure or cellular dynamics.

Cryo-immobilize your aqueous samples under high pressure with a unique freezing principle and uncover secrets of the cellular process.
Capture and resolve highly dynamic processes at the nanometer scale with millisecond precision.

The EM ICE solution, combining superior high pressure freezing with the possibility of light and electrical stimulation, is the platform for your discoveries.

Currently cryo-fixation is the only way to fix cellular constituents without introducing significant structural alterations. The EM ICE solution uses a unique, alcohol-free freezing principle to allow a superior cryo-fixation of the specimen enabling better quality results to be obtained:

No alcohol in the chamber leads to a faster pressure increase and immediate cooling of the specimen
No alcohol residue on the carrier or the specimen
Precisely define the timing for light and electrical stimulation

Leica EM ICE Location at DTU Nanolab Building 307

For further information on the equipment usage or training contact mktracy@dtu.dk [2].

Freeze substitution

Leica EM AFS2 and EM FSP (COMING SOON)

The Leica EM AFS2 performs freeze substitution and progressive lowering of temperature (PLT) techniques and allows low temperature embedding and polymerization of resins. The Leica EM FSP (freeze substitution processor), an automatic reagent handling system combined with the Leica EM AFS2, dispenses reagents for both freeze substitution and PLT applications. The LED illumination from within the chamber and the attached stereomicroscope for viewing and positioning of samples ensures ease of use.

For further information on the equipment usage or training contact mktracy@dtu.dk [3].

Microtome

RMC MT-7 Microtome

Our RMC MT-7 Microtome is a vintage piece of equipment and can be used for planning specimens for SEM/EDX and/or for cutting relative thin slices (approx. 200nm thick) for TEM. First, the specimen needs to be embedded into a resin or an epoxy, and then can be sliced with a glass or diamond knife.

Risk Assessment of RMC MT-7 Microtome: File:APV RMC Microtome.pdf

For further information about the microtome usage contact afull@dtu.dk [4].

Leica EM UC7 Ultramicrotome

The Ultramicrotome Leica EM UC7 provides easy preparation of semi- and ultrathin sections as well as perfect, smooth surfaces of biological and industrial samples for TEM, SEM, AFM and LM examination. Combining ergonomic design and innovative technology the Ultramicrotome Leica EM UC7 sets new standards in Ultramicrotomy. It offers a range of outstanding features and benefits of use for the ultramicrotomist, whether highly skilled or absolute beginners.

The Leica ultramicrotome is used for ultra thin sectioning of sample embedded in resin block with a feed range of 1 nm up to 15 µm. Glass or diamond knife can be used for the ultra sectioning of the samples.

The main steps of this technique proceed as follows:
1. Mount sample
2. Mount glass or diamond knife to knife holder
3. Trimming and ultrasectioning of sample
4. Fishing sections
5. Transfer to an EM grid
6. EM imaging

Operating manual: File:EM UC7 Operating manual.pdf

For further information about the equipment usage or training contact mktracy@dtu.dk [5].

Leica EM FC7 Cryo-Ultramicrotome

Within minutes the Leica EM UC7 ultramicrotome can change to a cryo-ultramicrotome by mounting the cryo chamber EM FC7. Cryo-sections (-15° to -185°C) can be prepared for TEM, SEM, AFM and LM.

The main steps of this technique proceed as follows:
1. Set up the cryo chamber EM FC7 to the EM UC7 apparatus
2. Mount both the trim and sectioning diamond knives to the knive holder and set up in the cryo chamber
3. Fill up liquid nitrogen Dewar
4. Set pump between the liquid nitrogen Dewar and the ultramicrotome apparatus
5. Let equipment to cool down for 1 hour
6. Meanwhile prepare samples
7. Mount sample
8. Trimming and ultrasectioning of sample
9. Collecting sections and transfer to an EM grid

Operating manual: File:EM FC7 Operating manual.pdf
Risk Assessment: File:Risk assessment - EM FC7 Cryo-Ultramicrotome.pdf

For further information about the equipment usage or training contact mktracy@dtu.dk [6].

KnifeMaker

LKB Knifemaker 7801A

At DTU Nanolab we offer the possibility to make glass knives using the LKB Knifemaker 7801A.

Manual of LKB Knifemaker 7801A: File:LKB Knifemaker 7800B Manual.pdf

LKB Knifemaker Location at DTU Nanolab Building 307 Room 906

For further information about the knifemaker usage and training contact mktracy@dtu.dk [7].

Critical point dryer

Leica EM CPD300

The Critical Point Drier (CPD) is used for drying samples for the SEM. The machine uses the fact that at the critical point the solvent can be converted from liquid to gas without crossing the interfaces between liquid and gas (no surface tension) and hence no sample drying artefacts. CO2 is the solvent of choice as its triple point is suitable for biological samples (31°C and 74 bars). The CO2 is not miscible with water; therefore the sample should be dissolved in acetone or ethanol.

Operating manual: File:EM CPD300 Operating manual.pdf
Risk Assessment: File:Risk assessment - EM CPD300 Critical Point Dryer.pdf

For further information on the CPD usage or training contact mktracy@dtu.dk [8].

Drying oven

The TS9026 drying oven is of 26L capacity and is used for epoxy embedding experiments.

For further information on the equipment usage contact mktracy@dtu.dk [9].

Mini tube rotator

The mini-tube rotator is designed for rotating various sized laboratory tubes at a variety of mixing angles at speeds ranging from 4 to 18 min–1. Ideal for mixing and separation processes involved in molecular biology, histochemistry and clinical applications.

Variable speed with LCD display
Digital microprocessor control
An adjustable 0 – 90° mixing angle
Interchangeable carousels for all common laboratory tubes
Cold room and incubator compatible

For further information on the equipment usage contact mktracy@dtu.dk [10].

Centrifuge

The Eppendorf Mini Spin plus centrifuge is a desktop centrifuge with supplied rotor with maximum speed/force 13,400rpm/12,100xG. It has a 30-minute timer, which is settable in 15-sec increments. It has a short-spin mode fixed at maximum speed. The Mini Spinner Eppendorf is located in building 314, in the Soft Mater (toxic) Lab.

For further information on the equipment usage contact mktracy@dtu.dk [11].

pH meter

If you are planning on doing chemical fixation on biological samples you will probably need to make buffers and use a pH-meter. The VWR pH-meter (model pH 1000L) is located in building 314, in the Soft Mater (toxic) Lab and it is dedicated to “Soft Matter” related work.

For further information on the equipment usage contact mktracy@dtu.dk [12].

Pulsing Vortex Mixer

VWR pulsing vortex mixer with features to suit different applications. The vortex mixer provide optimum comfort and minimal stress.

Can be used at 4 to 40 °C (maximum 85% relative humidity, non condensing), in an incubator, CO₂ incubator or cold room
Pulsing model has unique action which reduces heat generation and ensures efficient mixing and disruption
Digital and pulsing units have timer, 1 s to 160 h

For further information on the equipment usage contact mktracy@dtu.dk [13].

Sonic Dismembrator

The Fisherbrand Model 505 sonic dismembrator apparatus applies sound energy to agitate particles in a sample. In biological applications, sonication may be sufficient to disrupt or deactivate a biological material. For example, sonication is often used to disrupt cell membranes and release cellular contents. In nanotechnology sonication is commonly used for evenly dispersing nanoparticles in liquids.

For further information on the equipment usage contact mktracy@dtu.dk [14].

Sample preparation flowchart

For TEM imaging of biological sample at room temperature or cryo conditions:

For SEM imaging of biological sample at room temperature or cryo conditions:

For further information about the procedures contact mktracy@dtu.dk [15].

@@ Line 94: / Line 94: @@
 Operating manual: [[:File:EM UC7 Operating manual.pdf]]<br />
-Risk Assessment: [[:File:Risk assessment - EM UC7 Ultramicrotome.pdf]]<br />
 [[File:Leica EM UC7.jpg|400px|left|thumb|Leica EM UC7 Location at DTU Nanolab Building 307 Room 906]]<br clear="all" />