The present disclosure provides methods of collecting electron diffraction patterns from nanocrystals to obtain a three-dimensional structural model of a compound, as well as methods of identifying compounds and methods of determining polymorphic forms. In addition, the present disclosure provides methods of characterizing a first compound from a sample, as well as methods of screening compounds from a sample. The present disclosure also provides systems for characterizing a compound from a sample, which systems include modules for high-performance liquid chromatography, dispensing, and electron microscopy.

A refrigerant for a cooling device (10) comprising a cooling circuit (11) with at least one heat exchanger, in which the refrigerant undergoes a phase transition, the refrigerant being a refrigerant mixture composed of a mass fraction of carbon dioxide and a mass fraction of at least one other component, wherein the mass fraction of carbon dioxide in the refrigerant mixture is 10 to 50 mass percent, preferably 30 to 50 mass percent, the other component being pentafluoroethane and/or difluoromethane.

A refrigerant for a cooling device (10) comprising a cooling circuit (11) with at least one heat exchanger, in which the refrigerant undergoes a phase transition, the refrigerant being a refrigerant mixture composed of a mass fraction of carbon dioxide and a mass fraction of at least one other component, wherein the mass fraction of carbon dioxide in the refrigerant mixture is 10 to 50 mass percent, preferably 30 to 50 mass percent, the other component being pentafluoroethane and/or difluoromethane.

The invention relates to a device and method for determining a property of a sample that is to be used in a charged particle microscope. The sample comprises a specimen embedded within a matrix layer. The device comprises a light source arranged for directing a beam of light towards said sample, and a detector arranged for detecting light emitted from said sample in response to said beam of light being incident on said sample. Finally, the device comprises a controller that is connected to said detector and arranged for determining a property of said matrix layer based on signals received by said detector.

There is provided an automated system for preparing tissue samples that comprises one or more microtomes, a hydration system, and a processor, the processor being programmed to initiate facing, by one or more microtomes, of a first tissue block comprising a first tissue sample embedded in an embedding material, and cause the first tissue block to be hydrated by the hydration system for a first predetermined time, and initiate facing, by one or more microtomes, of a second tissue block while the first tissue block is being hydrated, the second tissue block comprising a second tissue sample embedded in an embedding material, and cause the second tissue block to be hydrated by the hydration system for a second predetermined time, and to initiate the one or more microtomes to begin sectioning of the first tissue block while the second tissue block is being hydrated.

A thermal cycling device includes a thermally-conductive carrier, a temperature adjustment device, a storage tank, and a liquid delivery device. The temperature adjustment device is thermally coupled with the thermally-conductive carrier. The storage tank is disposed corresponding to and abuts against the temperature adjustment device, or the temperature adjustment device is at least partially disposed in the storage tank. The liquid delivery device communicates with the storage tank. A temperature control method for the thermal cycling device can control whether liquid contacts the temperature adjustment device through the liquid delivery device in coordination with whether the temperature adjustment device heats the thermally-conductive carrier, so as to produce rapid heating and heat dissipation effects.

A thermal cycling device includes a thermally-conductive carrier, a temperature adjustment device, a storage tank, and a liquid delivery device. The temperature adjustment device is thermally coupled with the thermally-conductive carrier. The storage tank is disposed corresponding to and abuts against the temperature adjustment device, or the temperature adjustment device is at least partially disposed in the storage tank. The liquid delivery device communicates with the storage tank. A temperature control method for the thermal cycling device can control whether liquid contacts the temperature adjustment device through the liquid delivery device in coordination with whether the temperature adjustment device heats the thermally-conductive carrier, so as to produce rapid heating and heat dissipation effects.

The disclosure relates to a cryogen-free cooling apparatus for cooling a sample, comprising a vacuum chamber, a first cooling device which is configured to generate a first temperature in the vacuum chamber to provide a main thermal bath, a second cooling device, which is in connection with a sample stage on which a sample is to be arranged, wherein the second cooling device is a solid state cooler which is configured to provide a second temperature to the sample stage, and wherein the second temperature is different from the first temperature, and a sample loading device which is configured to change the sample while operating the first cooling device and the second cooling device, wherein the sample stage is held in the vacuum chamber by a plurality of first fibers of low thermal conductivity such that the sample stage is thermally decoupled from the main thermal bath.

The disclosure relates to a cryogen-free cooling apparatus for cooling a sample, comprising a vacuum chamber, a first cooling device which is configured to generate a first temperature in the vacuum chamber to provide a main thermal bath, a second cooling device, which is in connection with a sample stage on which a sample is to be arranged, wherein the second cooling device is a solid state cooler which is configured to provide a second temperature to the sample stage, and wherein the second temperature is different from the first temperature, and a sample loading device which is configured to change the sample while operating the first cooling device and the second cooling device, wherein the sample stage is held in the vacuum chamber by a plurality of first fibers of low thermal conductivity such that the sample stage is thermally decoupled from the main thermal bath.

Localized detection of RNA in a tissue sample that includes cells is accomplished on an array. The array include a number of features on a substrate. Each feature includes a different capture probe immobilized such that the capture probe has a free 3′ end. Each feature occupies a distinct position on the array and has an area of less than about 1 mm.sup.2. Each capture probe is a nucleic acid molecule, which includes a positional domain including a nucleotide sequence unique to a particular feature, and a capture domain including a nucleotide sequence complementary to the RNA to be detected. The capture domain can be at a position 3′ of the positional domain.