Methods for performing multiple omics analysis in parallel are provided, the methods can include: dividing the mixture of cells or cell components into at least a first portion and a second portion; performing a first analysis on the first portion to acquire a first set of analytical data; performing a second analysis on the second portion to acquire a second set of analytical data. Methods for forming mixtures of analytes into first and second portions are also provided. The methods can include aligning the first and second plates to engage the first exposed surface with the second exposed surface, wherein the engaging is sufficient to convey at least some of the first analytes into the second solution to form a second mixture of the first analytes.

Provided herein are systems and methods for a point of care apparatus. The point of care apparatus includes a fluid container for receiving a biosample, an intermediate cap, and a cartridge having at least one microfluidic channel.

Provided is a packaging container including a bag main body portion having a first surface, a second surface and an opening portion; and a tongue piece portion formed to be continuously extended from the first surface. The bag main body portion and the tongue piece portion have an aluminum vapor-deposited layer on an outside thereof, the packaging container further includes an adhesion portion which is provided on the second surface to be spaced from the opening portion; and a folded-back portion which is provided between the adhesion portion and the opening portion to fold back the tongue piece portion to the opening portion side. A length of the tongue piece portion is a, a length from the opening portion to the folded-back portion is b, and a length from the folded-back portion to the adhesion portion is c. And,
a<b+c.

An adapter for connecting an array of pipette tips having through bores with conical upper ends to a multichannel air displacement pipettor having a plurality of ports with compliant internal sealing surfaces. The adapter comprises a planar base with an array of openings extending between its top and bottom surfaces. Sealing tubes project upwardly from the top surface, and tip mounting tubes project downwardly from the bottom surface, with pairs of sealing tubes and tip mounting tubes being arranged coaxially and in communication with respective ones of the openings in the base. The tip mounting tubes are externally dimensioned and configured for insertion into the conical upper ends of the pipette tips, and the sealing tubes are externally configured and dimensioned for insertion into the ports of the pipettor and into sealing interengagement with their compliant internal sealing surfaces.

A device and method for filtering a liquid, wherein the device (100) comprises a container (110), a filter unit (120) and a filtering medium (130). The container (110) holds the liquid (10) containing a solid substance (10a), and the filter unit (120) is slidable in the container (110). The filtering medium (130) is non-permeable to the solid substance (10a) in the liquid (10).

Systems, methods, and apparatus are disclosed for recovering one or more target cells from a fluid sample. A first chamber aligned with a first surface of a removable filter receives the fluid sample. The removable filter defines a plurality of pores configured to retain the one or more target cells on the first surface and/or in the plurality of pores, each pore of the plurality of pores having a first diameter smaller than a diameter of the one or more target cells in the first surface and a second diameter greater than the first diameter in a second surface of the removable filter. A second chamber comprises a hydrophilic microporous wick structure configured to contact the second surface of the removable filter and capillarize any non-target cells and fluid from the fluid sample, drawing them into the second chamber.

The present invention addresses the problem of providing a fluid handling system that is capable of injecting a fluid into a desired chip or the like without using a large-scale device. In order to resolve the problem, this fluid handling system has a reservoir, a flow path chip, and a cap, one end of which is fitted to the internal opening of the reservoir and the other end of which is connected to an introduction port of the flow path chip, the cap having a through-hole that links the one end and the other end. In this fluid handling system, a protruding part provided to the flow path chip is fitted into the through-hole at the other end of the cap and restricts blocking of the through-hole when a fluid moves inside the through-hole of the cap.

The disclosed apparatus, systems and methods relate to a modular microfluidic device, the component comprising a channel comprising an apex opening, wherein the apex opening that is at least partially surrounded by a collar configured to pin a liquid within the channel. The modular microfluidic device may also have a structural tip in or near the apex opening which is configured to allow for the flow of the liquid into the channel from a second component for a modular microfluidic device when the component is engaged with the second component.

Disclosed is a system to separate, enrich, and/or purify a cellular population from a biological tissue, such as a tissue sample. For example, an adipose tissue sample can be acquired and disrupted. The disrupted tissue sample can then be separated and purified. The separated components can include multipotent, pluripotent, or other cell populations.

An embodiment in accordance with the present invention provides two devices for the isolation of rare cell populations such as circulating tumor cells (CTCs). Both devices use magnetic fields to manipulate cells that are bounded to paramagnetic particles (PMP). One device uses surface tension and a sieve for cell filtration, whereas the other allows for the direct transfer of cells onto a standard microscope slide. Subsequent processing steps may be directly performed on the devices thereby minimizing cell losses. The first device is referred to as the ST (surface tension) device and the second device is referred to as the DT (direct transfer) device. The ST device can also be considered as a chip for the isolation of the rare cell populations.