A sample consumable that carries a microvolume of sample to a sample loader. The consumable is precisely aligned utilizing a double-alignment feature to the loader. The loader is based on a crank-slider geometry and allows for simple, one-handed operation for the user. Overall, the consumable and sample loader increase reproducibility of in-line sample loading and offers ease-of-use.

A dispensing device for reducing the dead volume of a liquid sample includes a main channel connected to a sample inlet and a sample outlet, and branch channels connected to the main channel. Each branch channel is connected to a different liquid reservoir. High inflow-withstanding pressure sections are provided in the main channel between the branch channels and between the branch channel and the sample outlet. Each high inflow-withstanding pressure section has a channel inner wall forming a contact angle of 90 or larger with a liquid sample. A liquid sample enters the main channel through the sample inlet, reaches a branch point between the first branch channel and the main channel, flows into the first branch channel and the liquid reservoir, and then passes through the high inflow-withstanding pressure section to a branch point between the next branch channel and the main channel.

Systems and methods are described for operating an electroporation system with single cell resolution. The system controllably adjusts an (x,y) position of a multi-well plate to position a particular well relative to an electrode, a pipette, and a microscope camera that are stationary in the (x,y) plane. The same motorized (x,y) stage is also controlled to position a particular one of a plurality of interchangeable microfluidic probes (e.g., micropipettes) below a microfluidic probe coupler, wherein the coupler is also stationary in the (x,y) plane.

A vacuum assist apparatus can comprise a microplate. The microplate can comprise a first surface and an opposing second surface. A plurality of wells can be formed in the first surface of the microplate. Each of the plurality of wells can be sized to receive an assay therein. A support base can comprise a fluid passage. The microplate can be positioned adjacent and in contact with the support base. A pressure device, in fluid communication with the fluid passage, can exert a vacuum within the fluid passage to actively retain the microplate in the contact with the support base.

Systems and methods are described for a non-contact method for positioning a tip of an object. A light beam of known dimensions is projected and a position of the tip of the object relative to the light beam is adjusted. Light scatter indicative of the tip of the object being positioned within the dimensions of the light beam is detected and a position of the tip of the object is determined based at least in part on the known dimensions of the light beam and the detected light scatter.

A fully-automated biological slide specimen processing device and a method. The device mainly includes a testing assembly, a base platform, a Z-arm, an X-arm, a Y-arm, a dispensing nozzle and scanning devices for identifying a reagent and a specimen. The device in the present invention can automatically realize regular and quantitative dispensing according to testing process requirements and testing steps, automatically control the heating, automatically control liquid filling and liquid discharging, and realize full automation of the testing process. When the slide specimen needs a heat treatment, an insertion slot may be directly filled with liquid and be heated.

A titration module of biochip includes a base, a plurality of titration units, a plurality of pipelines, a transfer unit, and a control unit. The plural titration units and the plural pipelines are arranged above the base, and that the titration units each is provided, at its lower end, a needle element and a reservoir which are communicated with each other. The transfer unit is arranged on the base, and includes at least one driving device for driving, selectively, the plural titration units and the plural pipelines in a lateral direction (leftward and rightward), a longitudinal direction (frontward and rearward) and a vertical direction (upward and downward), respectively. The control unit is electrically connected with the transfer unit, and controls the same for switching, selectively, the plural titration units and the plural pipelines.

A system and method for isolating and analyzing single cells, including: a substrate having a broad surface; a set of wells defined at the broad surface of the substrate, and a set of channels, defined by the wall, that fluidly couple each well to at least one adjacent well in the set of wells; and fluid delivery module defining an inlet and comprising a plate, removably coupled to the substrate, the plate defining a recessed region fluidly connected to the inlet and facing the broad surface of the substrate, the fluid delivery module comprising a cell capture mode.

A system and method for isolating and analyzing single cells, including: a substrate having a broad surface; a set of wells defined at the broad surface of the substrate, and a set of channels, defined by the wall, that fluidly couple each well to at least one adjacent well in the set of wells; and fluid delivery module defining an inlet and comprising a plate, removably coupled to the substrate, the plate defining a recessed region fluidly connected to the inlet and facing the broad surface of the substrate, the fluid delivery module comprising a cell capture mode.

The machine is configured to perform an automated rapid plasma reagent (RPR) agglutination test or other agglutination test. The machine includes a sample rack with multiple sample locations thereon and a reagent rack for storing of reagent. A shaker assembly supports at least one microtiter plate or other well supporting structure thereon with a plurality of wells in the plate. An automated pipette accesses samples and reagent and deposits them within wells of the microtiter plate. The shaker assembly shakes multiple samples within the wells of the microtiter plate. Finally, a camera photographs the wells of the plate, preferably from above with a light source below and the plate at least partially transparent. The image is then analyzed in an automated fashion to determine whether a ring of contrast material has remained smooth indicative of a non-reactive sample or has agglutinated/clumped together indicative of a reactive sample.