A nucleic acid detection host includes a host body, a detection kit installation area, a sample heating area, a sampling area, and an image collection unit. The detection kit installation area is configured to detachably install a nucleic acid detection kit. The sampling area is disposed above the detection kit installation area and is connected to the detection kit installation area. The sampling area is configured to add a detection solution into the nucleic acid detection kit. The image collection unit is configured to collect an image of the nucleic acid detection kit. A nucleic acid detection device including the nucleic acid detection host is also disclosed. The nucleic acid detection device has a simple structure, which is portable, flexible, and convenient, and can be used at home.

A microfluidics device includes an inlet, a plurality of parallelized microfluidic channels, a splitter and a plurality of detection electrodes. The inlet receives a fluidic sample including biological particles. The parallelized microfluidic channels include interaction zones for analysis of the biological particles. The splitter transmits the fluidic sample into the parallelized microfluidic channels. Detection electrodes can conduct the analysis. Each detection electrode is shared among the parallelized microfluidic channels. The detection electrodes are spatially encoded electrodes arranged on locations of each of the parallelized microfluidic channels.

The present invention relates to a microfluidic device 100 for image multiplexing. The microfluidic device 100 comprises a base structure 110 comprising an optical window 140 and a fluid well insert 120 coupled to the base structure 110. The fluid well insert 120 is configured to retain a microscope slide 130 for mounting of a biological sample 150 within the microfluidic device 100. The fluid well insert 120 is also configured to provide a fluid to said biological sample 150. A fluid well insert lid 160 coupled to the fluid well insert 120 is also provided.

A sample collection kit for collecting plant samples, in particular algae samples for biomedical applications, comprises at least one sample container adapted to receive plant samples, a sensor arrangement having multiple sensors that can be used to capture sample data, a data recording device adapted to record the sample data, a tool arrangement having collection tools, which are adapted for harvesting the plant samples, and having processing tools, which are adapted for processing the plant samples, a container device adapted to receive the tool arrangement and the de-vice arrangement in a state that is isolated from the surroundings, and identification markings that include identification data and are attached to the at least one sample container, the collection tools and the processing tools, wherein there is provision for an authentication device that contains an electronically readable data carrier containing authentication data that represent a state of the sample collection kit, and the authentication device is attached to at least one from the container device, the at least one sample container, the collection tools and the processing tools. An authentication arrangement and a method for testing a state of a sample collection kit are also described.

The invention provides methods for stably immobilizing nucleic acid tracers onto surfaces of products and objects. This method is applied for the identification and authentication of the marked object or product. The present invention further provides specific coated articles and their use in product verification; processes for manufacturing such coated articles, methods for the verification of the coated article, methods for the quantification of the coated article blending, and products suitable for such verification and quantification method.

Provided herein is an analyzing system including components and methods thereof. The analyzing system includes, in some embodiments, a test cartridge and an analyzer. The test cartridge can include a port for a biological sample; one or more lateral flow assay strips with one or more target capture zones for binding one or more targets of the biological sample; and a memory device including a development time for the test cartridge. The analyzer can include an opening for the cartridge; a reader/writer device for writing an initial time stamp for the biological sample to the memory device and reading it back; a processor configured to execute an algorithm and logic to ensure an elapsed time from the initial time stamp meets or exceeds the development time for the test cartridge; and a detector for detecting emissions from an up-converting phosphor in the one or more target capture zones.

A test device is configured for diagnostic testing and includes an optical readable medium, in turn including a pattern of spots of material arranged on a surface of the device. Several patterns may be provided. The patterns accordingly formed may be human and/or machine readable. They may notably encode security information, e.g., indicating whether the device has already been used. The spots may notably be inkjet spotted. In addition, a method is provided for decoding information encoded in a pattern of such a test device. In embodiments, liquid is introduced in the device, which comprises additional spots having a substantially different solubility than spots forming the actual pattern. Thus, the additional spots get solubilized in and flushed by the liquid as the latter wets them, and an initially hidden pattern may be read, which is formed of the remaining spots (not solubilized). Encoding methods are also provided.

An apparatus includes a media that includes an encoded pattern to indicate a location of each of a plurality of dispensing locations on a receiving area for a pipette dispenser. The encoded pattern is employed to guide the pipette dispenser to dispense a volume to a selected dispensing location from the plurality of dispensing locations based on a predetermined dispensing location on the receiving area.

A method for automated processing of a sample using a first pipette tip container (110) having a first pipette tip comprises the steps of: removing the first pipette tip (160) from the first pipette tip container (110); feeding the sample into the first pipette tip container (110); processing the sample in the first pipette tip container (110). A rack (100) comprises at least one first pipette tip container (110) having a first pipette tip (160), wherein the rack (100) comprises means for identifying an alignment of an orientation of the rack (100) in a rack receptacle of an apparatus for automated processing of a sample. A transport arrangement comprises at least two racks (100), wherein at least one bottom region of a pipette tip container (110) of a first rack (100) is in direct contact with a releasable covering, in particular a tear-off film of a second rack (100).

It is an object to provide a cover slip sticking device capable of improving matching between types of clearing agents and cover slips. As a means for solving the problem, a cover slip sticking device includes a dipping bath (21) in which slide glasses (22) on which specimens are attached are housed to be dipped in a clearing agent, a holder (11) having a cover slip (10) and cover slip information (14), a mounting part (C) on which the holder is mounted, a sticking part (B) sticking the cover slip (10) taken out from the holder (11) on the slide glass (22), a reading unit (62) reading the cover slip information (14), a storage unit (65) storing a type of the clearing agent and matching information between types of clearing agents and types of cover slips and a determination unit (66) comparing the cover slip information (14) read by the reading unit (62) and the type of the clearing agent stored in the storage unit (65) with the matching information to determine whether the types match with each other or not.