A sample holder unit 400 capable of quickly and easily soaking a sample in a crystalline sponge, and of quickly and accurately performing single-crystal X-ray structure analysis, is provided. The sample holder unit comprises a sample holder 214 and an applicator 300. The applicator 300 comprises an opening 302 and a storing space in which the sample holder is stored; a seal part 304 provided on a contact surface with the sample holder stored in the storing space; and a pull-out prevention part 305 that prevents the sample holder from being pulled out from the opening 302, the pull-out prevention part engaged with the sample holder stored in the storing space.

A test device includes a housing and a carrier detachable from the housing. The housing includes a socket, and the carrier contains a testing element, and the carrier along with the testing element therein is capable of being inserted into the housing through the socket. The housing includes a blocking structure and a locking structure. The blocking structure and the locking structure are integrated to form a locking component. When the carrier is inserted into the housing, and a position of the carrier is locked by the locking structure, the carrier is abutted against the blocking structure. The carrier keeps stable after being inserted into the housing; and the carrier is located in the same position for each insertion.

A system for biological analysis includes a housing, a block assembly within the housing having a sample block and a baseplate, a heated cover and a cover carrier. The sample block receives a sample holder comprising an RFID tag. A first drive mechanism generates relative movement between the sample block and the baseplate along a first axis. A second drive mechanism generates relative movement between the heated cover and the cover carrier along a second axis that is different from the first axis. Based on a first command the first drive mechanism releasably engages the sample block and operates the second drive mechanism to releasably engage the heated cover with the cover carrier. The system also includes first and second RFID antennas that receive RFID data from the sample holder RFID tag that is read by at least one RFID reader.

A magnetic bead separation method includes: storing, in a container, a mixed liquid containing a magnetic bead and a liquid containing target molecules, and adsorbing the target molecules on the magnetic bead, the magnetic bead containing a Fe-based metal soft magnetic particle and a coating film with which the Fe-based metal soft magnetic particle is coated, and having a saturation magnetization of 50 emu/g or more and 250 emu/g or less; applying an external magnetic field to the container and magnetically attracting at least a part of the magnetic bead by the external magnetic field; and applying an acceleration to the container while the magnetic bead is magnetically attracted by the external magnetic field and desorbing the liquid adhering to the magnetic bead.

The present invention discloses an eco-friendly recyclable dropper, comprising a pressing portion and a pipette, wherein a bottom of the pressing portion is wrapped around a top of the pipette, wherein a bottom inner wall of the pressing portion includes a concave groove, wherein a top outer wall of the pipette includes a corresponding convex circle, wherein the concave groove matches with the convex circle and become airtight based on the characteristics of both material, wherein the pressing portion is made of PE material, wherein the pipette is made of PP material. Since the pressing head is made of PE material or a mixture material of PE and PP, and the pipette is made of PP material, a combination of the pressing head and the pipette is better in airtightness comparing to prior arts using glass pipettes; furthermore, the design of the pressing head and the concave groove and the convex circle of the pipette provides better airtightness; the dropper and the bottle of this invention both used PP and PE material, which can be fully recycled and reused after using the liquid within, avoids environmental pollution and saves resources. The market of this invention is very wide and this invention has a breakthrough meaning in the dropper field.

Methods and apparatus for long read, label-free, optical nanopore long chain molecule sequencing. In general, the present disclosure describes a novel sequencing technology based on the integration of nanochannels to deliver single long-chain molecules with widely spaced (>wavelength), ˜1-nm aperture “tortuous” nanopores that slow translocation sufficiently to provide massively parallel, single base resolution using optical techniques. A novel, directed self-assembly nanofabrication scheme using simple colloidal nanoparticles is used to form the nanopore arrays atop nanochannels that unfold the long chain molecules. At the surface of the nanoparticle array, strongly localized electromagnetic fields in engineered plasmonic/polaritonic structures allow for single base resolution using optical techniques.

The present invention relates generally to an apparatus that is able to provide a sealed chamber system including a cell sorter, that allows for various oxygen tensions of choice to be maintained during cell harvest, sorting (and isolation of sub-populations of cells), analysis, etc.

The invention is directed to a slide chamber comprising a top member (10), a fluidic seal (20), a transparent closure member (30) and base member (40) wherein the top member (10) is provided with at least one examination chamber (11) and a plurality of openings (12) positioned at two sides of the cover member outside of the examination chamber (11); and the base member (40) is provided with interconnecting means (41) complementary to the openings (12) of the top member characterized in that the interconnecting means (41) of the base member (40) and the openings (12) of the top member (10) are configured to mechanically interlock with each other by lateral movement thereby pressing the top member (10) against the transparent closure (30) member in a water-tight manner.

There is provided a histology system that comprises a microtome configured to expose a face of a tissue block comprising a tissue sample embedded in an embedding material and remove one or more tissue sections from the sample, a hydration system configured to hydrate the tissue block by depositing a hydrating liquid on the face of the tissue block, and a transfer system configured to transfer the one or more tissue sections from the microtome to one or more slides. In some embodiments, the hydration system is configured to produce droplet condensation of the hydrating liquid and deposit the condensation on the face of the tissue block.

The invention provides devices that improve tests for detecting specific cellular, viral, and molecular targets in clinical, industrial, or environmental samples. The invention permits efficient detection of individual microscopic targets at low magnification for highly sensitive testing. The invention does not require washing steps and thus allows sensitive and specific detection while simplifying manual operation and lowering costs and complexity in automated operation. In short, the invention provides devices that can deliver rapid, accurate, and quantitative, easy-to-use, and cost-effective tests.