30results about How to "Less testing" patented technology

Systems and methods analyzing body fluids such as blood and bone marrow are disclosed. The systems and methods may utilize an improved technique for applying a monolayer of cells to a slide to generate a substantially uniform distribution of cells on the slide. Additionally aspects of the invention also relate to systems and methods for utilizing multi color microscopy for improving the quality of images captured by a light receiving device.

The invention relates to slickened or siliconized flame resistant fiber blends that are well suited for use in mattresses, boxsprings, upholstered furniture, fiber-filled bed clothing, transportation seating or any end use application where a soft materials are desired for flame resistant (FR) purposes. Some of the fibers in the blend are slickened. The FR fibers incorporated into these blends include both char forming FR fibers and oxygen depleting FR fibers. FR char-forming fibers are those which exhibit little shrinkage when exposed to direct flame and are not spun from polymers manufactured with halogenated monomers. Oxygen depleting FR fibers are spun from polymers manufactured with halogenated monomers.

Systems and methods analyzing body fluids contain cells including blood, bone marrow, urine, vaginal tissue, epithelial tissue, tumors, semen, and spittle are disclosed. The systems and methods utilize an improved technique for applying a monolayer of cells to a slide and generating a substantially uniform distribution of cells on the slide. Additionally aspects of the invention also relate to systems and method for utilizing multi-color microscopy for improving the quality of images captured by a light receiving device.

Systems and methods analyzing body fluids contain cells including blood, bone marrow, urine, vaginal tissue, epithelial tissue, tumors, semen, and spittle are disclosed. The systems and methods utilize an improved technique for applying a monolayer of cells to a slide and generating a substantially uniform distribution of cells on the slide. Additionally aspects of the invention also relate to systems and method for utilizing multi-color microscopy for improving the quality of images captured by a light receiving device.

The present invention provides a system verification system that automatically generates a behavior model modeling the system under test in terms of actions of a test case and a range of expected reactions corresponding to those actions. In this regard, the system verification system obtains a set of actions and individual reactions corresponding to the actions from a plurality of runs of a test case for the system under test, and automatically generates the behavior model representing the system under test in terms of the set of actions and a range of expected reactions each range corresponding one of the actions. The range of expected reactions generalizes and includes all or most of the individual reactions corresponding to said one of the actions.

The invention provides a method for testing a semiconductor film, a manufacturing method of a semiconductor film, a laser crystallization method, a laser crystallization device, and a laser crystallization system, for testing a laser crystallized semiconductor film, which require less time, have sufficient reliability, are excellent in cost management and applicable to mass production. In the method for testing a semiconductor film having an improved crystallinity by irradiating an energy light, the tested semiconductor film is photographed in a dark field digital image and then the luminance of the digital image is calculated by a computer in a constant direction for testing.

Embodiments disclose a device for testing biological specimen. The device includes a sample carrier and a detachable cover. The sample carrier includes a specimen holding area. The detachable cover is placed on top of the specimen holding area. The detachable cover includes a magnifying component configured to align with the specimen holding area. The focal length of the magnifying component is from 0.1 mm to 3 mm. The magnifying component has a magnification ratio of at least 30.

Embodiments disclose a device for testing biological specimen. The device includes a sample carrier and a detachable cover. The sample carrier includes a specimen holding area. The detachable cover is placed on top of the specimen holding area. The detachable cover includes a magnifying component configured to align with the specimen holding area. The focal length of the magnifying component is from 0.1 mm to 8.5 mm. The magnifying component has a linear magnification ratio of at least 1. Some embodiments further include a multi-camera configuration. These embodiments include a first camera module and a second camera module arranged to capture one or more images of the first holding area and the second holding area, respectively. The processor may perform different analytic processes on the captured images of different holding areas to determine an outcome with regard to the biological specimen.

A method for producing micromechanical structures, in which a functional layer is deposited onto a sacrificial layer, and the sacrificial layer is removed again for the production of at least one mechanical functional element, which is characterized by a surface barrier layer, with which the functional layer begins on the sacrificial layer, and which has a different state from the remaining functional layer, is also removed at least to a considerable part, or, on the functional layer, one layer or a plurality of layers having at least approximately the same properties with respect to stress in the layer or layers such as the surface barrier layer is(are) applied. Additionally, a micromechanical structure having a functional layer in which the functional layer is constructed in such a way that the stresses are neutralized or no stress gradient appears.

Embodiments disclose a device for testing biological specimen. The device includes a sample carrier and a detachable cover. The sample carrier includes a specimen holding area. The detachable cover is placed on top of the specimen holding area. The detachable cover includes a magnifying component configured to align with the specimen holding area. The focal length of the magnifying component is from 0.1 mm to 8.5 mm. The magnifying component has a linear magnification ratio of at least 1. Some embodiments further include a multi-camera configuration. These embodiments include a first camera module and a second camera module arranged to capture one or more images of the first holding area and the second holding area, respectively. The processor may perform different analytic processes on the captured images of different holding areas to determine an outcome with regard to the biological specimen.

Embodiments disclose a device for testing biological specimen. The device includes a sample carrier and a detachable cover. The sample carrier includes a specimen holding area. The detachable cover is placed on top of the specimen holding area. The detachable cover includes a magnifying component configured to align with the specimen holding area. The focal length of the magnifying component is from 0.1 mm to 8.5 mm. The magnifying component has a linear magnification ratio of at least 1.

An image processing method to sample the image to generate patches. Feature vectors are extracted from the patches, and the extracted feature vectors are partitioned into clusters, where feature vectors in the same cluster share a common characteristic. A portion of interest in the image is segmented. An aggregate bounding region creation process is carried out by finding the largest segment and creating a bounding box around it; determining which cluster contains the most patches within the bounding box of the segment; and adding the patches of the determined cluster to an aggregate bounding region for the portion of interest. The aggregate bounding region creation process is repeated for each other segment in order of size. The resulting aggregate bounding region contains all the patches associated with the portion of interest. The patches which fall outside the resulting aggregate bounding region are then removed from the image.

The invention relates to the technical field of preparation of biological functional materials, in particular to a double-emission fluorescent molecularly imprinted polymer nanoparticle and its preparation method and application. In the present invention, carbon quantum dots are coated in silica nanospheres as the inner core of a ratiometric fluorescent probe, and then red cadmium telluride quantum dots are used as response signals, and acrylamide and 4-vinylphenylboronic acid are used as bifunctional single Using N,N-methylenebisacrylamide as a cross-linking agent and dopamine as a template molecule in the alcohol phase through the initiation of azobisisobutyronitrile to synthesize a dual-emission fluorescence with a specific recognition site for dopamine Molecularly imprinted polymer nanoparticles, and then prepared a fluorescent detection test paper with visualization effect by impregnation method, so as to realize the visual detection of DA, and the detection results of DA in human serum samples proved that the fluorescence detection paper prepared by this method The detection test paper can be used for semi-quantitative detection of DA in actual complex samples.

The invention discloses a method for rapidly identifying the milled rice rate of indica type rice variety, and belongs to the technical field of method for measuring rice quality. The method comprises the following steps of: dividing indica type rice into three varieties, namely long-grained variety, medium-grained variety and short-grained variety, according to grain length condition of the variety; weighing the three varieties of fresh rice and placing the three varieties of fresh rice into a baking box for baking respectively; baking the long-grained variety of fresh rice in the baking boxof 50 DEG C for 6 hours or in the baking box of 60 DEG C for 4 hours; baking the medium-grained variety of fresh rice in the baking box of 50 DEG C for 8 hours or in the baking box of 60 DEG C for 4 hours; and baking the short-grained variety of fresh rice in the baking box of 50 DEG C for 8 hours or in the baking box of 60 DEG C for 5 hours to obtain the milled rice rate measured by a national standard method. The fresh rice which is just harvested is directly adopted for measurement, so the method has the advantages that: a small amount of rice is consumed, the method is convenient to operate, the efficiency is greatly improved, the baking time is short, the operating temperature is low and the safety performance is high, the efficiency of the entire measurement of the milled rice rate is improved and simpler and more accurate judgment basis is provided for related research works.

A composite liquid crystal panel that interacts with an inspection station to simulate operating liquid crystal displays, and methods of fabricating and testing such liquid crystal panels. The composite liquid crystal panel enables the application of operating voltages to a plurality of unit liquid crystal panel areas. The inspection station provides operating power, illuminating light, and first and second polarizers. When power is applied to the composite liquid crystal panel an image is produced. That image will show defects in the unit liquid crystal panel areas. Beneficially, the inspection station tilts to enable easier problem identification.

A method for printing on a printing machine with color space transformation using tables formed of n-dimensional orthogonal grids includes printing and colorimetrically measuring a test chart in a target color space providing measured values corresponding to sampling points in the color space, interpolating between the sampling points to determine further sampling points, and using existing sampling points to create an ICC table for color space transformation between target and process color spaces. A computer isolates combinations of n−1-dimensional partial grids for process color combinations from grids of the table in the process color space. Partial grids are converted into two-dimensional segments. Sampling points of segments are modified, removing nonrequired sampling points and distributing sampling points in the partial grid. The partial grids are reintegrated into the grid and color management of the printing operation and the printing operation using the reduced ICC table occurs.

A mobile telephone can be configured to interact with external services by using a client application on the telephone that interacts with several external services via an intermediary server. The server sends, to the mobile telephone, configuration information to enable or disable defined sets of functionality in the application, the configuration information depending on and appropriate to the particular external service selected on the mobile telephone and being sent automatically to the mobile telephone over-the-air. An implementation of the invention enables a single client application on the mobile telephone to automatically configure features on / off, and modify the terminology used in resources (such as menus, text strings, bitmap images, sounds, sonic effects etc.) depending on the external system or service that the client is connected to via the intermediary server.