The present disclosure relates to a specimen collection device comprising ventilation means for drying a collected specimen. The device further comprises a cassette into which the specimen collected is secured to maintain evidentiary chain of cus tody requirements while providing unobstructed access to a collected specimen for automated analysis. Methods of using the device are also provided.

A sample preparation system includes a sample input, a first chamber fluidly coupled to the sample input and containing a sample preparation reagent, a second chamber containing a surface enhanced Raman spectroscopy (SERS) sensor structure and a third chamber containing a sensor preparation solution. The sample input, the first chamber and the second chamber are fluidly coupled to one another in a series and the third chamber is fluidly coupled to the third chamber outside of the series so as to sequentially direct a sample received by the sample input through the first chamber to the second chamber and out of the second chamber and so as to direct the sensor preparation solution into the second chamber following discharge of the sample out of the second chamber.

A pressurizable sample system includes a microplate having a planar plate surface and several sample wells. Each sample well has a flange positioned circumferentially around an outer surface of the sample well and against the planar plate surface. The sample system further includes a capping plate with a planar cap surface and several caps projecting from the planar cap surface. Each cap has a geometrical configuration in complementary correspondence with the configuration of the sample well.

A device for testing the constituent elements of a fluid compound is provided. The device includes a hollow chamber that is filled with a sample fluid. At one end of the hallow chamber, a transfer fluid (such as air) is pumped through a permeable membrane. A portion of the sample fluid permeates the permeable membrane and is absorbed into the transfer fluid. The transfer fluid, with the absorbed sample fluid now in gaseous phase, is sent to a testing device in order to determine the constituent elements of the sample fluid.

The present invention provides a non-cryopreservation method that enables inexpensive and stable storage of feces. More specifically, the present invention provides: (A) a storage method of feces, the storage method including drying the feces in the presence of a solid desiccant; (B) a hermetic container including: (a) a solid desiccant; and (b) feces under the non-contact state with the solid desiccant; and (C) a feces fixing article including: (a) one or more members containing or fixing a solid desiccant; and (b) feces under the contact state with the solid desiccant. As the solid desiccant, a water absorbing solid desiccant such as silica gel is preferred.

Provided herein are portable biocontainment devices for safe and reliable collection of biological samples, including liquid and gas samples. A sample inlet for collecting fluids and/or gases, including oral fluids and expired breath samples, is connected to a container having a climate-controlled container reservoir. One or more sample containers are connected to the sample inlet for collection of samples. The devices are configured for safe transport and handling of samples, while maintaining sample viability, including for relatively long transport periods. Safety components integrated within the device facilitates safe and effective decontamination of contagious samples. In this manner, aborting the sample preservation by decontamination prior to a hazardous release is achieved within the same apparatus.

A method for the regulated humidification and temperature control of a gas mixture in an inner chamber of an incubator, which inner chamber is sealed off from the surroundings by a housing, includes conducting heat from at least one condensation surface inside the incubator, which at least one condensation surface is separate from the inner surfaces of the inner chamber, is conducted out of the incubator to the outside through a wall delimiting the inner chamber by a heat conductor. Outside the incubator, the heat conductor is connected to a cooling body which releases the heat to the relatively cold ambient air. The method allows dispensing with a cooling unit and at the same time avoid sources of contamination due to moisture condensing out.

Apparatus and methods are provided relating to evaporation of solvents from samples and to prolonging the time taken to carry out an evaporation procedure. A cap for engaging with an open end of a sample container comprises an engaging surface for engaging with the open end, and a body portion which extends over the open end. The body portion is preformed to define an opening which provides a fluid pathway between the open end of the container and the surroundings of the container, such that the cap impedes vapor flow from a sample in the container to the surroundings of the container. A holder for receiving a plurality of such caps is also provided and a method of evaporating a solvent from a sample in a sample container is described.

Sample tube adapters dimensioned to fit into one or more sample tubes in order to prevent carryover or contamination between sample tubes that are adjacent to one another during one or more stages of sample preparation. Methods for use of such sample tube adapters and methods for preventing carryover or contamination between sample tubes that are prepared adjacent to one another are also described. The apparatus described herein was developed to mitigate or eliminate cross-well contamination identified in high-throughput assays, e.g., 96-well based assays. In one embodiment, the apparatus is designed to fit onto the top of a standard 96-well plate and is kept in place during one or more stages of sample preparation, e.g., the entire forced-air drydown portion of sample preparation.

Devices and methods for manual and high-throughput protein crystal growth and growth of other biological and organic crystals. A microplate includes a plurality of cells and a frame that defines the cells in the microplate. In each cell there is at least one well open at top. Each well in a cell may be enclosed at bottom, or it may be open at bottom, in which case the well bottom may be sealed by a separate part, which may be, e.g., a separate film or plate (e.g., of plastic, glass or metal) or a molded part.