A closure and a container assembly are disclosed. The closure includes a first visual identifier and a second visual identifier, wherein the second visual identifier is different from the first visual identifier. The first visual identifier may be a first color, and the second visual identifier may be a second color. At least one of the first and/or second visual identifier may include a fluorescent compound having a characteristic fluorescent spectra. The first visual identifier and the second visual identifier may be provided on the annular skirt of the closure. The fluorescent compound may be provided on at least one of the closure and the container assembly and can be used to facilitate automated visualization of the fluorescent compound under fluorescence excitation light.

A test strip system having containers and suitable carriers therefor. The test strip assembly is suitable for carrying out different types of chemical, biological or biochemical tests and evaluating them using a suitable analysis device. The test strip assembly has a first region having at least one container and a second region also having at least one container. The container of the first region has a flat transparent bottom, and the container of the second region has a V-shaped or U-shaped bottom.

A sample container cap (or “cap”) is configured to be used with a sample container for collecting fluids. The cap has a body and a shutter connected to the body. The cap has a (1) first, open position in which at least one body opening and at least one shutter opening are not aligned and the cap is configured so that fluid cannot readily pass therethrough, (2) second, open position in which the at least one body opening and the at least one shutter opening are aligned and the cap is configured so that fluid can pass therethrough, and (3) third, closed and locked position, in which the at least one shutter opening and the at least one body opening are not aligned and fluid cannot readily pass through the cap, and the cap is configured to not be moved to an open position.

Automation compatible removable lids are provided. The removable lids include a top surface surrounded by a peripheral rim. The removable lids further include septal portions configured to receive an extractor, such as a pipette tip, inserted therethrough. The septal portions are further configured to grip the extractor to facilitate lid removal.

A specimen collection assembly and method for detecting the same are disclosed. The specimen collection assembly includes a specimen collection container having an open top end, a closed bottom end, and a sidewall extending therebetween defining an interior adapted to receive a biological specimen. The specimen collection container also includes first indicia containing information. The assembly further includes a cap having thereon second indicia, the cap being removably engagable with the open top end of the container. The second indicia contains the same information as the first indicia.

This disclosure relates to portable devices for detecting various virus antibodies for the detection of virus diseases. Viral infections, such as those from SARS-CoV family viruses, HIV family viruses, and other family viruses can be detected by their antibodies or DNA in a clinical specimen.

A plurality of caps are provided each with a visual coding of color and/or indicia for use with different sizes of bottles at least in accordance with a height of the bottles from a closed bottom end to an open top end for engaging each of the caps. Each of the caps has a tube mounted to, or through, an aperture extending through a top closed end of the cap to extend a selected length enabling one end of the tube to reach or extend along an interior surface of the bottom end of any of the bottles of the height to which the cap is coded for use therewith. The other end of tube is extendable to a bioreactor container. Each of the caps has another tube or port to another aperture of the cap to provide an air vent with an optional air filtering device.

The self-contained kit comprises methods for receiving and preparing the biological samples for the nucleic acid amplification and sensing the presence of the target assay. The kit consists of a self-heating pack to provide the heat for nucleic acid sample preparation and amplification processes. The change of the amplification is indicated through colorimetric or turbidity sensing and detected through a mobile phone camera and associated mobile application for photographic scanning of physical or chemical differences of the samples to produce the test results.

A reverse transcriptase quantitative polymerase chain reaction based analyzing system includes a sampling tube. The sampling tube includes a tube portion, a cap coupled to the tube portion via a ratchet locking mechanism. The system comprises a microfluidic processing unit coupled to the sampling tube. An intake system receives pre-registered, sealed microfluidic labs into the system, and disinfects them before processing begins. The microfluidic processing unit comprises a piezo electric type ribonucleic acid extraction and concentration unit coupled to the sampling tube, an eluent storage unit, an eluate dosing chamber, an analysis settling chamber with a bubble removal area, an assay rehydration unit, an assay analysis unit and a no-target control analysis unit.

Provided are a PCR tube that can reliably perform management of a sample, and an RFID sample management system and an RFID sample management method using the PCR tube. The PCR tube 40 includes a tube body 42 that has an opening at one end and has a collar part 46 around the opening, and a lid part 44 that is attachably and detachably mounted on the tube body 42 and seals the opening of the tube body 42 at the time of the mounting. An RFID tag 48 having a passive antenna built therein is provided at the collar part 46 or the lid part 44, and the antenna has directivity in a direction opposite to a bottom face 42a of the tube body 42.