There is disclosed a fluid distribution system for distributing fluid from a single source to a plurality of downstream receptacles. The system has a distribution manifold with a single inlet and a plurality of outlets arrayed around a circumferential outer periphery. The outlets may be directed to the different receptacles which each have their own vent filter, or each receptacle connects back to the distribution manifold for common venting.

A system for a deep-sea planktonic microorganism in-situ concentration, temperature maintaining and pressure maintaining sampling is provided and includes a sampling cylinder body with double layer structures, the sampling cylinder body is provided with a plug-shaped inner cavity, the plug-shaped inner cavity is provided with a transfer water outlet and a water inlet connected to a water inlet component, the plug-shaped inner cavity is connected to an end cover, the plug-shaped inner cavity is connected to a filter part, the sampling cylinder body is provided with a sampling water outlet, the sampling water outlet is respectively connected to a pressure maintaining device and a water outlet pipe, a temperature maintaining material layer and a temperature control component are connected between the double layer structures, and the temperature control component is electrically connected to a controller. The system can complete sampling on the premise of maintaining in-situ pressure of samples.

The present technology is directed to extraction devices, systems, and methods for controllably withdrawing and transferring fluid samples, such as blood, from a sample collection container to a testing device. For example, some embodiments of the present technology provide fluid extraction devices that include a fluid control module, a housing containing a receiving element and a suction element, and an actuator. To transfer blood from a sample collection container to a testing device, a user places the sample collection container over the receiving element and inserts the testing device into an outlet of the fluid control module. The user then pushes a lever or otherwise actuates the actuator, which automatically withdraws a predetermined volume of blood from the sample collection container and transfers it to the testing device positioned at the outlet of the fluid control module.

A blood cell analysis method and a blood cell analyzer are provided. In the method and analyzer, characteristic information of white blood cell fragments is obtained based on side scattered light information and fluorescence information, characteristic information of platelets is obtained based on forward scattered light information and fluorescence information and then a count value for the platelets is acquired based on the characteristic information of the platelets and the characteristic information of the white blood cell fragments. The present invention can avoid the influence of the white blood cell fragments on the platelet counting, thereby ensuring the accuracy of the platelet counting without increasing costs.

The present disclosure relates to an automated system for sampling an egg that includes an egg manipulator to hold and orient one or more eggs in a defined position; an opener for opening the outer shell of the egg; an extractor for removing a sample from the allantois of the egg, and which preferably includes a system to apply increased gas pressure to the extractor up to the moment of contact with the egg; a system to clean the opener or extractor before or after removing a sample from the egg; and a sealing unit for closing the opening of the egg with a sealer.

There is disclosed a fluid distribution system for distributing fluid from a single source to a plurality of downstream receptacles. The system has a distribution manifold with a single inlet and a plurality of outlets arrayed around a circumferential outer periphery. The outlets may be directed to the different receptacles which each have their own vent filter, or each receptacle connects back to the distribution manifold for common venting.

Liquid level sensing apparatus are disclosed. An example liquid level sensing apparatus includes a cannula defining a body having a tip and an access channel. The tip to pierce a container, where the cannula is to be at least partially positioned in the container when the tip pierces the container. A probe is to be positioned in the access channel. A signal source is to electrically energize the probe and the cannula to cause the probe to emit a first signal and cause the cannula to emit a second signal.

A sample filtration and/or extraction system includes a vacuum manifold configured to connect with a vacuum pump, a vacuum chamber such that each of a plurality of filter columns or the filter plate is configured to be disposed at least partially within the vacuum chamber, the plurality of filter columns or the filter plate including a plurality of openings configured to receive a sample, and a passive pressure decoupling device configured to be placed on a top of the plurality of filter columns or the filter plate, such that each of the plurality of openings of the plurality of filter columns or the filter plate is covered by the passive pressure decoupling device. The passive pressure decoupling device includes a reserve air volume structure above each of the plurality of openings.

In an embodiment, an optical system comprises an optical cell having an interior fluid chamber defined by an interior surface of a housing, a process inlet disposed in the housing and in fluid communication with the interior fluid chamber, and a process outlet disposed in the housing and in fluid communication with the interior fluid chamber, wherein the process inlet and process outlet facilitate the flow of a fluid through the interior fluid chamber. A sampling outlet can be disposed in the housing and in fluid communication with the interior fluid chamber. A first bi-directional pump can be in fluid communication with the sampling outlet and a first storage vessel and can be configured to withdraw a first sample of the fluid via the sampling outlet and to cause the first sample to flow into the first storage vessel.

An automatic sampling apparatus for taking liquid samples for the qualitative or quantitative determination of at least one analyte contained in the sample liquid includes a sample line that can be fluidically connected to the sampling station, a pump device, at least one sample container that can be fluidically connected to the sample line, and an electronic control system. The electronic control system is configured to fluidically connect the sample line to the sample container such that a fluid flow path extending from the sampling station through the sample line into the sample container is formed. The electronic control system is further configured to transport, using the pump device, a definable volume of the sample liquid, in the form of a liquid sample, along the fluid flow path into the sample container. The sampling apparatus is configured for concentrating or extracting the analyte present in the liquid sample.