Abstract:
A method of neural stimulation is described for maintaining the responsiveness of electrically excitable cells to repeated electrical stimulation. A stimulating signal (23) is applied to the electrically excitable cells. The stimulating signal is repeatedly applied (26, 29, 32, 35) with a progressively increasing signal strength. A quiescent period (44) may be interleaved between bursts (43, 45) of stimulation. The electrically excitable cells may be retinal cells.
Abstract:
A pico projector includes a light-emitting diode module, collimators, a lens array, magnification lenses, a reflection mirror, a polarizing beam splitter, an LCoS (light crystal on silicon) panel, and an image lens module, wherein the light-emitting diode module emits red, green, and blue lights. The collimators convert light from the light-emitting diode module into collimated light. The lens array homogenizes the collimated light. The magnification lenses magnify the homogenized light from the lens array with a predetermined ratio to be projected onto the LCoS panel. The reflection mirror changes direction of the light path. The polarizing beam splitter allows for transmission of a horizontal polarization light component and reflects a vertical polarization light component. The LCoS panel reflects and modulates the light to form an optic signal. The image lens module includes, in sequence, positive, positive, negative, positive, and positive lenses to project the optical signal to a screen.
Abstract:
A detachable top tube apparatus includes two tubes, two spring-biased detents, two hooks, two latches and an elastic element. The tubes are telescopically connected to each other. Each of the spring-biased detents is connected to a related one of the tubes. Each of the hooks includes a portion inserted in a related one of the tubes. Each of the latches each including two wings pivotally connected to a related one of the tubes between a releasing position and a locking position. In the releasing position, each of the latches allows a portion of a bicycle to be hooked by and unhooked from the related hook. In the locking position, each of the latches retains the portion of the bicycle hooked by the related hook. The elastic element interconnects the tubes.
Abstract:
A dual-panel micro reflective liquid crystal projection device is provided for improving brightness of projected image, including a set of two reflective liquid crystal panels respectively arranged at top side and right side of a polarizing beam splitter so that a light beam emitting from a light source located at bottom side of the beam splitter is received and split by the beam splitter into a horizontal polarization component and a vertical polarization component, which are then respectively reflected and modulated by the two reflective panels into vertically polarized light and horizontal polarized light for simultaneously transmitting identical image signals to a projection system arranged at left side of the beam splitter to thereby double the brightness of the image projected onto a screen.
Abstract:
A pico projector includes a light-emitting diode module, collimators, a lens array, magnification lenses, a reflection mirror, a polarizing beam splitter, an LCoS (light crystal on silicon) panel, and an image lens module, wherein the light-emitting diode module emits red, green, and blue lights. The collimators convert light from the light-emitting diode module into collimated light. The lens array homogenizes the collimated light. The magnification lenses magnify the homogenized light from the lens array with a predetermined ratio to be projected onto the LCoS panel. The reflection mirror changes direction of the light path. The polarizing beam splitter allows for transmission of a horizontal polarization light component and reflects a vertical polarization light component. The LCoS panel reflects and modulates the light to form an optic signal. The image lens module includes, in sequence, positive, positive, negative, positive, and positive lenses to project the optical signal to a screen.
Abstract:
A bicycle parking rack comprises a base member provided on the ground and including a first flat portion and a second flat portion respectively defined at first and second ends thereof and attach the ground, and with a wheel of a bicycle disposed between the first and second flat portions; and a support member including a coupled portion formed on a first end thereof and detachably coupling to the base member and a holding portion formed on a second end thereof and extending from the coupled portion, and with the coupled portion provided between the first and second flat portions.
Abstract:
This invention is about the capacitor assembly improvement of electrical circuit system, including a central partitioning board, its surface has connecting hole installed through conductive component, both sides are distributed with insertion slots; first base board installed with sleeve hole connecting to one end of conductive component and an insertion hole corresponding to the insertion slot, its one side is soldered with multiple capacitors; and second base board, having a sleeve hole connecting to the other end of the conductive component and the insertion hole corresponding to the insertion slot, one side is soldered with multiple capacitors; thus the conductive component is inserted through central partitioning board and assemble the first and second base boards to both ends of the conductive component, to replace cable layout to form electrical connectivity, so that the problem of electrical circuit system of prior art having noise and high assembly cost can be overcome.
Abstract:
A rack is disclosed for regulating the parking of bicycles. The rack includes a base that provides flexibility in length and at least one pair of restraints installed on the base. The base includes a first lateral tube, a second lateral tube and at least one pair of transverse tubes. The first lateral tube includes a central portion and two ends extending from the central portion. The second lateral tube includes a central portion and two ends extending from the central portion. Each transverse tube includes a first end connected to one of the ends of the first lateral tube and a second end connected to one of the ends of the second lateral tube. The pair of restraints is installed on the pair of transverse tubes.
Abstract:
This invention characterizes the specific peptide fragment derived from specially prepared zinc charged fetuin and a method of preparation thereof, wherein the fragment was found to contain an apoptosis-inducing activity. Specifically, the amino acid sequence of this peptide is H-T-F-S-G-V-A-S-V-E and correlates to amino acid no. 300-309 of fetuin, referred to herein as Fetuin Peptide Fragment (FPF 300-09). FPF 300-09 strongly induced apoptosis in LNCaP (prostate cancer) and HT-29 (colon cancer) cells without affecting CCD 18 Co (normal colon) cells. The in vitro tissue culture study demonstrated that the FPF 300-09 is more potent than the parent molecule (full-length zinc charged fetuin) in inducing apoptosis. FPF 300-09 has a LD50 of 0.3-0.4 &mgr;M, while the LD50 for zinc-charged fetuin is 3-10 &mgr;M.
Abstract:
The present invention provides the methods to isolate the proteins specifically induced apoptosis (programmed cell death) in prostate cancer cells (LNCAP), leukemia cells (HL-60), and breast cancer cells (MCF-70), but without effect in normal human lung fibroblast cells (CCD 39 Lu). P-1 has no effect on breast cancer cells. Five proteins have been isolated from the conditioned media of culture cells: (1) Apogen P-1: the proteins (Apogen P-1a, Apogen P-1b and Apogen P-1c) isolated from the conditioned medium of XC cells are able to induce apoptosis in prostate cancer cells (LNCAP) without effect in normal human lung fibroblast (CCD 39 Lu), colon cancer (T84), breast cancer (MCF-7) and leukemia (HL-60) cells. (2) Apogen P-2: the protein isolated from the conditioned medium of C3H1OT1/2 cells is able to induce apoptosis in prostate cancer cells (LNCAP) and breast cancer (MCF-7) without effect in normal human lung fibroblast (CCD 39 Lu) and colon cancer (T84) cells. (3) Apogen L: the protein isolated from the conditioned medium of XC cells is able to induce apoptosis in leukemia cells (HL-60), and breast cancer (MCF-7) without effect in normal human lung fibroblast (CCD 39 Lu), colon cancer (T84) and prostate cancer (LNCAP) cells. The isolated protein Apogen P-2 is at least in part comprised of bovine fetuin. When properly prepared, fetuin is able to induce apoptosis in leukemia cells (HL-60), prostate cancer (LNCaP and PC-3) cells, colon cancer (Colo 205) cells, breast cancer (MCF-7) cells, and lung cancer (Calu-1) cells. The in vivo tests done with fetuin have shown an increased life span for mice bearing leukemia. The invention may lead to the discovery of a novel class of anticancer drug that aims at prostate cancer, breast cancer, leukemia and other cancers by inducing apoptosis in cancer cells without affecting normal cells.