Abstract:
The present invention provides a mutant antibody comprising a reactive site not present in the wild-type of the antibody and a antigen recognition domain that specifically binds to a metal chelate, wherein the reactive site is in a position proximate to or within the antigen recognition domain.
Abstract:
An apparatus for power generation. The apparatus has a first substrate comprising a conductive surface region and a second substrate coupled to the first substrate. Preferably, the second substrate comprises an electret material region, which is characterized by a substantially uniform electric field associated with the electret material region. The conductive substrate and the electret substrate are aligned in a significantly parallel fashion with a common area of each region directly facing the other region (A). A distance (d) characterizing a spatial separation is formed between the conductive surface region and the electret material region. A relative voltage potential (V) between the conductive substrate and the electret substrate is associated with the distance (d). In between the conductive substrate and the electret substrate is a material, liquid, gas, or combination with an associated permittivity (null0). The relative voltage potential changes based upon a change in the spatial separation between (d), a change in the overlapping area (A), or a change in the permittivity (null0) between the conductive surface region and the electret material region.
Abstract:
This invention provides approaches to improve the signal to noise ratio (S/N) in electrochemical measurements (e.g. amperometry, voltammetry, etc.). In particular, a method is described wherein the faradaic current is temporally dissociated from the charging current associated with reading the charge of a redox-active species (e.g. a self-assembled monolayer (SAM)). This method, designated herein as open circuit potential amperometry (OCPA), quantitatively reads the charge of the redox species bound to (electrically coupled to) an electrode surface, while discriminating against both charging current(s) and amperometric signal(s) that arise, e.g. from diffusion-based species in solution.
Abstract:
The invention provides methods and compositions for replicating a polynucleotide sequence independent of replication of chromosomal DNA in a cell.
Abstract:
Methods for treating one or more diseases associated with neutral sphingomyelinase 2 (nSMase2) in a subject in need of treatment thereof, the method comprising administering to the subject a therapeutically effective amount of 2,6-dimethoxy-4-(5-phenyl-4-thiophen-2-yl-1H-imidazol-2-yl)-phenol (DPTIP) or a pharmaceutically acceptable salt thereof, are disclosed.
Abstract:
An intracellular monitoring device (IMD) that fits completely inside a living cell, and causes no significant impairment, to a cell's normal biological processes. The IMD monitors a cell for its level of a biological substance (e.g., calcium ion concentration) of interest. If the biological substance reaches or exceeds a threshold, the IMD transmits an electromagnetic signal, received by an antenna outside the cell. Each IMD has its electromagnetic signal encoded with a unique frequency. Detection of the frequency components, in the signals received by an antenna, permits identification of the source IMD's. A high calcium ion concentration is indicative of a strongly-activated cerebral cortex neuron. Brain tissue is relatively transparent to near infrared, making it a good frequency band, for the electromagnetic signals from neuron-monitoring IMD's. The near infrared of each IMD can be produced by quantum dots, powered by bioelectric catalysis triggered by high calcium ion concentration.
Abstract:
Systems and methods are disclosed for human balance training. The systems and methods involve intermittently occluding the vision of a subject while the subject is engaged in a balance activity, such as walking on a balance beam, for example. Creating a brief period of continuous visual occlusion results in posterior parietal cortex activation, leading to enhanced balance training. The end result is much greater improvement in balance compared to physical training alone.
Abstract:
Provided herein are methods of determining a subject's metastatic potential, comprising measuring a level of expression of a gene, an RNA, or a protein, or a combination thereof, in a sample obtained from a synthetically-engineered pMN implanted in the subject, wherein the measured expression level of the gene, RNA, or protein in the sample is compared to a control level. Related methods are also provided herein.
Abstract:
A device configured for wireless power transfer includes a digital controller configured to generate a plurality of switch control signals, and a transceiver configured to generate a wireless signal for the wireless power transfer. The transceiver includes a plurality of switches, each switch of the plurality of switches being responsive to a respective switch control signal of the plurality of switch control signals such that the wireless signal has a waveform shaped in accordance with a code sequence for the wireless power transfer. The code sequence is one of a set of predetermined code sequences, each predetermined code sequence being orthogonal to each other predetermined code sequence of the set of predetermined code sequences.
Abstract:
Novel human interleukin-2 (IL-2) muteins or variants thereof are provided. In particular, provided are IL-2 muteins that have an increased binding capacity for IL-2RP receptor and a decreased binding capacity for IL-2RΥc receptor, as compared to wild-type IL-2. Such IL-2 muteins are useful, for example, as IL-2 partial agonist and antagonists in applications where reduction or inhibition of one or more IL-2 and/or IL-15 functions is useful (e.g., in the treatment of graft versus host disease (GVHD) and adult T cell leukemia). Also provided are nucleic acids encoding such IL-2 muteins, methods of making such IL-2 muteins, pharmaceutical compositions that include such IL-2 muteins and methods of treatment using such pharmaceutical compositions.