Various embodiments herein disclose a device, comprising one or more fluid interfacing components and a cartridge holder, wherein the one or more fluid interfacing components are fixed while the cartridge holder moves along a linear guide. Also disclosed herein are methods of using the device to analyze a sample containing particles, and methods of diagnosing a disease in a subject by using the device.

A method, system and storage medium for providing an alarm for indicating that an abnormality is present in a sample analyzer are provided. The method includes: mixing a first aliquot of a blood sample with a diluent agent to prepare a first test sample; mixing a second aliquot of the blood sample with a lytic reagent to prepare a second test sample; detecting electrical impedance signals of the first test sample; detecting at least two types of optical signals of the second test sample; acquiring first platelet detection data based on the electrical impedance signals; acquiring second platelet detection data based on the at least two types of optical signals; acquiring an evaluation result based on a difference between the first platelet detection data and the second platelet detection data; determining whether the evaluation result meets a preset condition to provide an alarm.

A number analyzing method, a number analyzing device, and a storage medium for number analysis are disclosed, which enable, with high accuracy, analysis of the number or number distribution of particulate or molecular analytes according to the kinds of the analytes. A computer control program is executed on the basis of a data group of particle-passage detection signals which are detected by a nanopore device in accordance with passage of subject particles through a through-hole. Also, a particle type distribution estimating program is executed, to estimate probability density on the basis of a data group based on feature values indicating feature of the waveforms of pulse signals which correspond to the passage of particles and which are obtained as the particle-passage detection signals. Thus, the number of particles can be derived for each particle type.

A number analyzing method, a number analyzing device, and a storage medium for number analysis are disclosed, which enable, with high accuracy, analysis of the number or number distribution of particulate or molecular analytes according to the kinds of the analytes. A computer control program is executed on the basis of a data group of particle-passage detection signals which are detected by a nanopore device in accordance with passage of subject particles through a through-hole. Also, a particle type distribution estimating program is executed, to estimate probability density on the basis of a data group based on feature values indicating feature of the waveforms of pulse signals which correspond to the passage of particles and which are obtained as the particle-passage detection signals. Thus, the number of particles can be derived for each particle type.

A pulse baseline value calculation method and a particle counting method of a blood cell analyzer. The said pulse baseline value calculation method, within pulse non-duration time, if an absolute value of a difference value between any two adjacent data of n continuous sampled data is less than a baseline threshold, and the n continuous sampled data are closest to a pulse starting point, an average value of the n continuous sampled data is calculated, and the average value is a pulse baseline value. The present invention has the advantages of setting the baseline threshold and performing comparison, avoiding the sampled data of the baseline where the noise is superimposed, selecting the sampled data with noise or interference within an allowable range for calculation, avoiding accumulating the noise on the final baseline value, making the baseline value be closer to the real data, greatly reducing the erroneous judgment of the baseline value, and making the particle count be more accurate. The method of the present invention can be applied to the particle counting of 3-diff hematology analyzers, 5-diff hematology analyzers, flow cytometers and other biochemical instruments.

A pulse baseline value calculation method and a particle counting method of a blood cell analyzer. The said pulse baseline value calculation method, within pulse non-duration time, if an absolute value of a difference value between any two adjacent data of n continuous sampled data is less than a baseline threshold, and the n continuous sampled data are closest to a pulse starting point, an average value of the n continuous sampled data is calculated, and the average value is a pulse baseline value. The present invention has the advantages of setting the baseline threshold and performing comparison, avoiding the sampled data of the baseline where the noise is superimposed, selecting the sampled data with noise or interference within an allowable range for calculation, avoiding accumulating the noise on the final baseline value, making the baseline value be closer to the real data, greatly reducing the erroneous judgment of the baseline value, and making the particle count be more accurate. The method of the present invention can be applied to the particle counting of 3-diff hematology analyzers, 5-diff hematology analyzers, flow cytometers and other biochemical instruments.

The present disclosure provides a particle analyzer and a particle test control method and device thereof. A method comprises, acquiring a blood sample in a test location; preparing a diluted sample by the acquired sample; after acquiring a diluted sample, monitoring whether a pore blocking event occurs during a counting process; when the pore blocking event occurs, suspending the test of the sample, and performing an unblocking operation; and after the unblocking operation is completed, re-counting the same diluted sample without re-acquiring and re-diluting the blood sample by the impedance method after the unblocking operation.

The present disclosure provides a particle analyzer and a particle test control method and device thereof. A method comprises, acquiring a blood sample in a test location; preparing a diluted sample by the acquired sample; after acquiring a diluted sample, monitoring whether a pore blocking event occurs during a counting process; when the pore blocking event occurs, suspending the test of the sample, and performing an unblocking operation; and after the unblocking operation is completed, re-counting the same diluted sample without re-acquiring and re-diluting the blood sample by the impedance method after the unblocking operation.

A measuring cuvette for counting and/or characterizing cells, the measuring cuvette including a base and a transparent lateral enclosure extending from the base so as to form with the latter an optical measurement chamber; the base having a through-orifice with a diameter of 30 to 100 μm for cells to pass through, characterized in that the base and the transparent lateral enclosure form a one-piece cuvette suitable both for impedance measurement and for optical measurement. Also, a system for characterizing cells, which includes the measuring cuvette.

A sample analyzer prepares a measurement sample from a blood sample or a body fluid sample which differs from the blood sample; measures the prepared measurement sample; obtains characteristic information representing characteristics of the components in the measurement sample; sets either a blood measurement mode for measuring the blood sample, or a body fluid measurement mode for measuring the body fluid sample as an operating mode; and measures the measurement sample prepared from the blood sample by executing operations in the blood measurement mode when the blood measurement mode has been set, and measuring the measurement sample prepared from the body fluid sample by executing operations in the body fluid measurement mode that differs from the operations in the blood measurement mode when the body fluid measurement mode has been set, is disclosed. A computer program product is also disclosed.