A pipette tip made of plastic with an elongated tubular body with a lower opening at the lower end for the passage of liquid and an upper opening at the upper end for clamping onto an attachment of a pipetting device, wherein a seating region for the attachment is present next to the upper opening on the inner circumference of the tubular body, wherein at least one flattened area extending in the axial direction is present next to the upper opening on the outer circumference of the tubular body, the wall thickness of the tubular body gradually decreases in a cross-section through the tubular body, starting from one of the two regions of the tubular body adjoining the flattened area, in the flattened area towards its central region, and the flattened area has in the cross-section through the tubular body a straight or a less strongly curved profile than the adjoining regions.

Provided herein are a system, kit and methods that allow quick and precise detection, identification and quantification of analytes in liquid samples. The kit may be used in automated and pre-programmed singleplexed and multiplexed detection and quantification of one or more analytes in a liquid samples. The kit may include a chip caddy, consumable assay chips, an electrode assembly, an electrical connector assembly, one or more cables, a voltage supply, a vacuum pump, a vacuum trap, custom-designed manifolds, one or more buffers, reagents and instructions for use.

The present disclosure pertains to sample preparation devices useful for affinity capture and purification that include one or more internal structures that comprise a reservoir, a well, a fluid passageway, sorbent particles, and a filter element that blocks passage of the affinity sorbent particles, which sample preparation devices combine the attributes of both dispersive and flow through designs into a single sample preparation device. The present disclosure also pertains to kits that contain and methods that use such sample preparation devices.

An automatic liquid transfer optimization pipetting apparatus and method is disclosed. Namely, a liquid handling apparatus includes a pump supplying a nozzle (i.e., a pipette tip) via a conduit, one or more pressure sensors, and an electronic controller, and wherein the pipette tip is submerged in a liquid. Further, a method of automatic liquid transfer optimization pipetting includes the steps of actuating the pump to move a designated volume of liquid and then allowing the system to settle to a steady state after completion of pump actuation.

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.

Pipette assembly comprising a pipette device, a pipette tip, and an expanding mandrel collet coupling device coupling the tip to the pipette device, the coupling device comprising: circumferentially spaced apart segments, an annular base disposed below the segments and comprising a distal portion, an elastomeric element circumscribing the distal portion, and upwardly extending circumferentially spaced apart arms attached at first ends to the annular base and having upper free ends each supporting a different one of the segments configured to expand between a first and a second greater circumference for engaging a first interior working surface of the tip in concurrence with the elastomeric element sealing against a second interior working surface below the first surface and in concurrence with an abutment between a disk exteriorly disposed about a medial portion of the arms and a stepped interior shoulder of the tip disposed between the first and second working surfaces.

A non-displasive pipette is provided. The non-displasive pipette is configured for connection to a tip having a fluid therein. The tip includes an orifice to allow for the discharge of the fluid therefrom. The non-displasive pipette includes a body defining a chamber therethrough and having first and second opposite ends. The second end of the body is configured for connection to the tip. A plunger is slidably received in the chamber at the first end of the body. The plunger is moveable in the chamber between an extended position and a discharge position wherein the fluid is urged from tip through the orifice. An air discharge arrangement is configured to allow air from the chamber to escape therefrom and to maintain the fluid in the tip in response to connection of the second end of the body to the tip.

The present invention provides a disposable pipette tip for dispersive solid phase extraction (SPE) that allows for rapid, automatable purification of large biomolecules, such as nucleic acids, proteins and polypeptides without the need for additional tools such as centrifuges, magnetic plates or vacuum manifolds. The pipette tip is designed for optimal biomolecule isolation while maintaining sample integrity. Optimized methods of using the dispersive pipette extraction system for isolation of large biomolecules are also provided.

A microfluidic droplet generator that includes a body, an inlet arranged adjacent an upper surface of the body, and a sample reservoir adapted to contain a reservoir fluid that is immiscible in water. The sample reservoir includes a floor and a sidewall coupled to the floor. The floor extends along a horizontal axis and the sidewall extends along a vertical axis substantially perpendicular to the horizontal axis. The microfluidic droplet generator also includes one or more microchannels fluidly connecting the inlet to the sample reservoir. Each of the microchannels includes an inlet end and a reservoir end, and the reservoir end of each of the microchannels intersects the sidewall of the sample reservoir at a location beneath the upper surface of the body.

A pipette tip (20) containing a rigid porous matrix (22) on which a ligand is immobilized, the ligand being capable of binding to a protein associated with chromatin; the rigid porous matrix being positioned within the pipette tip such that, in use, chromatin in a liquid sample passing through the pipette tip is retained by the rigid porous matrix is described. A method of isolating chromatin from the liquid sample using the pipette tip and the use of the pipette tip in a chromatin immunoprecipitation assay are also described.