Abstract:
Embodiments include transmitters, wireless devices, and methods for performing loop delay and gain control. In a transmitter, a gain application element receives and combines digital input samples and a digital gain signal to generate gain-compensated digital samples. A power amplifier receives and amplifies an analog version of the gain-compensated digital samples to generate an antenna output signal. A feedback path generates an analog feedback signal from the antenna output signal, to produce a sequence of digital feedback samples from the analog feedback signal, and generates the digital gain signal from the sequence of digital feedback samples and a loop gain estimate. A loop delay and gain calculator calculates a loop delay estimate from the gain-compensated digital samples and the sequence of digital feedback samples, and calculates the loop gain estimate using the loop delay estimate, the gain-compensated digital samples, and the sequence of digital feedback samples.
Abstract:
The present disclosure provides a white blood cell differentiation reagent comprising a fluorescent dye compound of Formula I, wherein R1, R2, R3, R4, Y− and n are as defined in the specification. The present disclosure also provides a white blood cell detection kit comprising the white blood cell differentiation reagent, and a method of differentiating white blood cells using the white blood cell differentiation reagent.
Abstract:
An adhesion bond between a metallic surface layer and a second surface is formed by treating the layers with a material comprising sulphur-containing molecules. The sulphur-containing molecules are applied as a surface treatment of the surfaces, so that the sulphur-containing molecules act as a coupling agent to bond chemically to both substrates form nanometer-sized structures on the surfaces. The nanometer-sized structures are incorporated into a self-assembly interlayer in between the surfaces, with the interlayer forming a bond to both surfaces.
Abstract:
The present disclosure provides a reagent for blood analysis which may include: (1) a compound having the general formula I as a fluorescent dye, wherein n, X, R1, R2, R3, R4, R5 and Y− are as defined in the specification; (2) a surfactant selected from cationic surfactants, zwitterionic surfactants and anionic surfactants. The present disclosure also provides a method to perform blood analysis including the following steps of: (a) mixing the blood sample with the reagent for blood analysis disclosed to form a cell suspension; (b) detecting the scattered light signals and fluorescence signals from the cells; and (c) differentiating and counting the cells in the blood in terms of the scattered light signals and fluorescence signals.
Abstract:
Cyanine compounds having the general formula I for staining biological samples, wherein R1, R2, X, Y, A1 and A2 are as defined in the specification. These kinds of compounds may show good light illumination stability, have a maximum absorption peak around 640 nm that may not change as a function of ambient temperature, have rapidly increased fluorescence intensity upon binding to nucleic acids to form compound/nucleic acid complexes, and have a light spectrum in the near-infrared region, thereby effectively reducing interference from background fluorescence and increasing the accuracy of the detection when used as a staining agent for nucleic acids in a flow cytometer. The compounds provided can be used as a staining agent for erythroblasts in the blood.
Abstract:
A method of creating intracellular artificial nanostructures in situ, which employees a chemical precursor. The precursor does not self-assemble due to the presence of a cleavable motif linked to it. When the precursor comes inside live cells by an uptaking mechanism on the cell membrane, the cleavable motif is then to be removed by an enzymatic action of a first enzyme. Without the cleavable motif, the precursor now engages in a self-assembling process to form nanostructures within the live cells, which may cause formation of a hydrogel. Furthermore, the self-assembling process can be made reversible by employing a second enzyme which puts the cleavable motif back to the precursor, whereby dissolving the nanostructures into solution.
Abstract:
Techniques and technologies are provided for compressing differential samples of bandwidth-limited data and coding the compressed differential samples to reduce bandwidth and power consumption when communicating bandwidth-limited data over a serial interface which couples one integrated circuit to another integrated circuit.
Abstract:
The present disclosure provides a white blood cell differentiation reagent comprising a fluorescent dye compound of Formula I, wherein R1, R2, R3, R4, Y− and n are as defined in the specification. The present disclosure also provides a white blood cell detection kit comprising the white blood cell differentiation reagent, and a method of differentiating white blood cells using the white blood cell differentiation reagent.
Abstract:
A network processor system includes a network processor 1, which is provided with a number of interfaces 9, 11, 13, 15, 19, including one or more Ethernet interfaces 9, 11 and a UART interface 19, which can be used to load a software package into the network processor 1. The software package can thus be modified when required, or when the software package previously stored in the network processor system is corrupted. The Ethernet data packets received on the Ethernet interfaces 9, 11 are in a special format, which the network processor 1 can recognize, to distinguish them from conventional Ethernet packets. Thus, the network processor 1 does not have to be programmed to handle the full range conventional Ethernet data packets. The network processor 1 is provided with a second external non-volatile data storage device 7 in the form of a EEPROM memory 7. The EEPROM memory 7 provides a writable extension of the internal ROM memory of the network processor. It can, for example, be used to store the parameters of other components of a network processor system (e.g. a flash memory 5) so that the network processor 1 can be used in conjunction with components of a wide range of types.
Abstract:
The synthesis of thiophene based conducting polymer molecular actuators, exhibiting electrically triggered molecular conformational transitions is reported. Actuation is believed to be the result of conformational rearrangement of the polymer backbone at the molecular level, not simply ion intercalation in the bulk polymer chain upon electrochemical activation. Molecular actuation results from π—π stacking of thiophene oligomers upon oxidation, producing a reversible molecular displacement that leads to surprising material properties, such as electrically controllable porosity and large strains. The existence of active molecular conformational changes is supported by in situ electrochemical data. Single molecule techniques have been used to characterize the molecular actuators.