Abstract:
Methods for probing multiple targets in a biological sample are provided. The methods include the steps of providing a biological sample containing multiple targets, binding at least one fluorescent probe to one or more target present in the sample, and binding at least at least one control probe to one or more target present in the sample. The methods include the steps of observing a signal from the fluorescent probe and a control signal from the control probe and applying to the sample a basic solution containing an oxidizing agent that selectively inactivates the fluorescent probe and not the control probe. The methods further include the steps of binding at least one fluorescent probe to one or more target present in the sample and observing a signal from the fluorescent probe. The methods disclosed herein also provide for multiple iterations of binding, observing, and oxidizing for deriving information about multiple targets in a single sample. An associated kit is also provided.
Abstract:
A system for analyzing tissue samples, that generally comprises, a storage device for at least temporarily storing one or more images of one or more cells, wherein the images comprise a plurality of channels; and a processor that is adapted to determine the extent to which a biomarker may have translocated from at least one subcellular region to another subcellular region; and then to generate a score corresponding to the extent of translocation.
Abstract:
Methods for detecting multiple targets in a biological sample are provided. The methods includes contacting the sample with a first probe; physically binding the first probe to a first target; observing a first signal from the first probe; applying a chemical agent to modify the first signal; contacting the sample with a second probe; physically binding the second probe to a second target; and observing a second signal from the second probe. The methods disclosed herein also provide for multiple iterations of binding, observing, signal modification for deriving information about multiple targets in a single sample. An associated kit and device are also provided.
Abstract:
A system for analyzing tissue samples, comprising: a storage device for at least temporarily storing one or more images of one or more cells, wherein at least one of the images is indicative of one or more channels comprising a receptor tyrosine kinase (RTK); and a processing device that determines an extent to which one or more of the RTKs may have translocated from at least one subcellular region to another subcellular region of one or more of the cells; and generates a score based at least in part on the RTK translocation.
Abstract:
PROBLEM TO BE SOLVED: To reduce costs and to enable a probe to be held by hands by mounting an eddy current detection coil to a substrate so that it can be rotated freely, rotating it around the ordinate line of a first elastic member, and allowing an eddy current probe to have a means for measuring the rotary angle of the axial line in the longitudinal direction of the eddy current detection coil around the ordinate line for a reference direction being fixed to the substrate. SOLUTION: An eddy current detection coil 20 is mounted to a substrate 22 so that it can be rotated freely and can rotate around an ordinate line 28. Also, an eddy current probe 10 has a means for measuring the rotary angle of the ordinate line in the longer direction of the eddy current detection coil 20 around the ordinate line 28 for the reference direction being fixed to the substrate 22. Further, the eddy current probe 10 is mounted to a second surface 26 of the substrate 22 and includes a signal amplifier 64 that is electrically connected to the eddy current detection coil 20, thus improving an S/N ratio and hence improving the detection of a flaw.
Abstract:
Methods for probing multiple targets in a biological sample are provided. The methods include the steps of providing a biological sample containing multiple targets, binding at least one fluorescent probe to one or more target present in the sample, and binding at least at least one control probe to one or more target present in the sample. The methods include the steps of observing a signal from the fluorescent probe and a control signal from the control probe and applying to the sample a basic solution containing an oxidizing agent that selectively inactivates the fluorescent probe and not the control probe. The methods further include the steps of binding at least one fluorescent probe to one or more target present in the sample and observing a signal from the fluorescent probe. The methods disclosed herein also provide for multiple iterations of binding, observing, and oxidizing for deriving information about multiple targets in a single sample. An associated kit is also provided.
Abstract:
A closed loop automated method for staining of a biological sample is provided. The method comprises providing a biological sample, staining at least a portion of the biological sample by flowing in a reagent, monitoring one or more optical characteristics of the biological sample, and calculating a figure of merit based on at least one of the optical characteristics. An automated device for iterative staining of a biological sample is also provided.
Abstract:
An eddy current probe (10) is provided which can be moved by hand to a surface to be tested. A toroidal-shaped first resilient member (14) contacts the bottom face of a support member (12). An elastic membrane (16) extends over the bore (33) of the first resilient member (14), contacts the bottom lateral surface of the first resilient member (14), and is unattached to the radially inward-facing surface of the first resilient member (14). A more elastic, second resilient member (18) is placed in the bore (33), is unattached to the first resilient member (14), and contacts the bottom surface of the elastic membrane (16). A flexible, surface-conformable, eddy current sensing (20) coil overlies a portion of the bottom side of the second resilient member (18).
Abstract:
A novel micro optical system as a platform technology for electrical and optical interconnections, thermal and mechanical assembly and integration of electronic, optoelectronic, passive and active components. This platform provides optical coupling and chip-to-chip interconnection by microwave electrical, optical guided and unguided waves, and power or bias electrical contacts or interfaces by a novel chip in flexible circuit, rigid or inflexible embodiments.
Abstract:
A novel micro optical system as a platform technology for electrical and optical interconnections, thermal and mechanical assembly and integration of electronic, optoelectronic, passive and active components. This platform provides optical coupling and chip-to-chip interconnection by microwave electrical, optical guided and unguided waves, and power or bias electrical contacts or interfaces by a novel chip in flexible circuit, rigid or inflexible embodiments.