Apparatus (2) for testing a liquid specimen, which apparatus (2) comprises: (i) a container (4) for the liquid specimen; (ii) a lid (6) for closing the container (4) after the liquid specimen has been provided in the container (4); (iii) first securing means (8) by which the lid (6) is secured to the container (4); (iv) a test capsule (10) for securing to the lid (6) when the lid (6) is on the container (4); (v) second securing means (12) by which the test capsule (10) is secured to the lid (6); and (vi) a response chart (14) which is operable in response to contact with the liquid specimen, and the apparatus (2) being such that: (vii) the lid has an openable portion (18) which when opened permits a liquid specimen in the container (4) to enter the test capsule (10); (viii) the test capsule (10) has opener means (20) for opening the openable portion on the lid (6) when the test capsule (10) is secured to the lid (6); and (ix) the response chart (14) is inside the test capsule (10) and is contacted by the liquid specimen when the liquid specimen enters the test capsule (10).

Devices, methods and systems are provided for reducing the sample volume required for analysis. Inserts placed within a sample container, and substitute sample containers having smaller volume sample chambers are provided. Methods are provided for detection and quantification of target substances in reduced volume samples. Methods include placing a small-volume of sample in a small-volume insert. Methods include diluting a small-volume sample, and placing the diluted sample in a small-volume insert. Methods include reducing the volume of sample, and: increasing illumination; increasing dye concentration or amount; increasing the amount of an enzyme substrate; increasing the amounts, concentration, or labeling of antibodies for detection; increasing optical detector sensitivity; increasing the path length of light passing through the sample; decreasing the separation between sample and detector; altering the wavelength, or polarization, or number of wavelengths, passing through the sample; increasing electronic amplification of electrical signals; altering assay temperature; and other alterations.

A tube holder assembly includes a base plate, an attachment plate, and an optional securing element. The base plate may include guides into which protrusions of the attachment plate slide to alter the positioning apparatus from an open position to a closed position. The base plate also includes receivers to receive tubular members, which have their movement restrained by the receivers and the securing elements in the closed position. The tube holder assembly may also include a latch to help maintain the closed position during operation.

Disclosed in the present disclosure is a fixed volume pipette, including: a top bulb, a connecting tube, an overflow-storing tube, and a liquid-sucking tube; in the present disclosure, the upper and lower ends of the liquid-sucking tube are respectively designed as a conical structure, wherein the upper end inner cavity of the liquid-sucking tube is in a conical structure tapering from the bottom up, and the lower end inner cavity of the liquid-sucking tube is in a conical structure tapering from the top down.

The disclosure relates to a sample container holding and/or transporting device having an aperture with a longitudinal axis, which aperture is configured for receiving a sample container, wherein a biasing structure is provided in the aperture, which comprises a plurality of elastically deflectable nubs, wherein the nubs are distributed spatially discrete along the longitudinal axis of the aperture. The disclosure further relates to a use of a structure having nubs as a biasing structure in a sample container holding and/or transporting device, and to a laboratory automation system comprising a sample container holding and/or transporting device.

A tube holder assembly includes a base plate, an attachment plate, and an optional securing element. The base plate may include guides into which protrusions of the attachment plate slide to alter the positioning apparatus from an open position to a closed position. The base plate also includes receivers to receive tubular members, which have their movement restrained by the receivers and the securing elements in the closed position. The tube holder assembly may also include a latch to help maintain the closed position during operation.

Magnetic assisted separation apparatuses for separating a target substance from a medium in which the target substance is suspended, and related methods, are provided. According to one aspect, a magnetic separator may include a frame having an opening configured to receive one or more containers containing the medium. Additionally, the magnetic separator may include first and second magnetic field generating elements mounted on opposing sides of the frame such that one or more containers can be positioned between the first and second magnetic field generating elements. According to another aspect, a workstation includes a work surface for receiving one or more containers containing the medium, a fluid transfer member, an automated manipulator configured to move the fluid transfer member, and a plurality magnetic field generating elements each being moveable between a position remote from the one or more containers and another position adjacent to the one or more containers.

Devices, methods and systems are provided for reducing the sample volume required for analysis. Inserts placed within a sample container, and substitute sample containers having smaller volume sample chambers are provided. Methods are provided for detection and quantification of target substances in reduced volume samples. Methods include placing a small-volume of sample in a small-volume insert. Methods include diluting a small-volume sample, and placing the diluted sample in a small-volume insert. Methods include reducing the volume of sample, and: increasing illumination; increasing dye concentration or amount; increasing the amount of an enzyme substrate; increasing the amounts, concentration, or labeling of antibodies for detection; increasing optical detector sensitivity; increasing the path length of light passing through the sample; decreasing the separation between sample and detector; altering the wavelength, or polarization, or number of wavelengths, passing through the sample; increasing electronic amplification of electrical signals; altering assay temperature; and other alterations.

The present invention relates to a container for storing a reagent, the container comprising: a storage space for reagent (R) comprising a flexible pouch; a passage having a first end (4) that opens onto the outside of the container and a second end that opens into the storage space, the passage being designed to allow a sampling device (20) to access the storage space; a deformable partition (7) that closes off the passage when said partition is not mechanically loaded and which can be loaded by the sampling device to a position in which the passage is open; a seal (6) that is positioned in the passage and comprises an elastically deformable rim (64) defining an orifice (61) that is designed to receive part of the sampling device (20), said rim (64) being designed to establish a seal together with the outer walls of the sampling device when said device is introduced into the passage.

A digital slide scanning apparatus slide stage is configured to hold 1×3 and 2×3 glass slides. The slide stage is configured to alter its position by lateral shift or rotation to present the 1×3 or 2×3 sized recess to a slide rack for loading of the slide onto the stage. Also, a removable insert may configure the stage to hold a 1×3 glass slide when present and to hold a 2×3 glass slide when removed. Alternatively, a gripper stage is described herein that includes a fixed arm and a movable arm, each with one or more contact points configured to engage a side surface of the glass slide. Once the glass slide is secured between the contact points of the movable arm and the contact points of the fixed arm, the slide is further processed for scanning.