Abstract:
Provided is a pain-related compound, a pain-related pharmaceutical composition, and use of the same. Provided in one or more embodiments is a compound represented by Formula (I), a prodrug of the same, or a pharmaceutically permissible salt of any of the same.
Abstract:
The object of the present invention is to provide an antibody capable of immunologically and specifically binding to a folate receptor α and a folate receptor β. Specifically, the present invention relates to an antibody or a fragment thereof, in which the amino acid sequences of CDRH1, CDRH2, and CDRH3 of a heavy chain variable region (VH) are SEQ ID NOs: 2, 4, and 6, respectively, and the amino acid sequences of CDRL1, CDRL2, and CDRL3 of a light chain variable region (VL) are SEQ ID NOs: 10, 12, and 14, respectively.
Abstract translation:本发明的目的是提供能够免疫和特异性结合叶酸受体α和叶酸受体bgr的抗体。 具体地,本发明涉及其中重链可变区(VH)的CDRH1,CDRH2和CDRH3的氨基酸序列分别为SEQ ID NO:2,4和6的抗体或其片段, 轻链可变区(VL)的CDRL1,CDRL2和CDRL3的氨基酸序列分别为SEQ ID NO:10,12和14。
Abstract:
A fastening force auxiliary device (1) includes a seat part (10) in which a hole (11) allowing a screw part (3) of a miniscrew (2) to be inserted through is formed and which receives a head part (5) of the miniscrew (2). Further, the fastening force auxiliary device (1) has three spiked portions (13) extending from a periphery of the seat part (10) in a driving direction of the miniscrew (2). The spiked portions (13) extend so as to spread outward from the periphery of the seat part (10) and so as to gradually taper off. When the miniscrew (2) is implanted and fixed in a jaw bone or the like in an oral cavity, it is screwed into the jaw bone or the like while the screw part (3) is inserted through the hole (11) of the fastening force auxiliary device (1). Consequently, a flange (7) is received by the seat part (10) and tips of the spiked portions (13) come into pressure contact with a surface of the jaw bone or the like by being pressed by the flange portion (7). Consequently, it is possible to greatly reduce the failure of the miniscrew (2).
Abstract:
An image processing apparatus (100) is formed including: color image acquisition means (222) for acquiring a color image of an object, which is expressed by a luminance signal, a first color difference signal that is a color difference signal of a color pair that is easy to be identified by a dichromat and a second difference signal that is a color difference signal of a color pair that is difficult to be identified by the dichromat; color difference signal processing means (223) for performing mixing reprocessing that mixes a component of the second color difference signal with a component of the first color difference signal, for each pixel data of the color image; and display control means (230) for performing control to display the color image processed by the color difference signal processing means (223) on a display unit (109) as a color image subjected to color conversion. By this means, it is possible to provide a mechanism in which a dichromat can understand the hue of an object without learning.
Abstract:
The present invention provides a method for detection of a basic peptide by mixing a sample suspected to contain the basic peptide and a reagent containing denatured albumin and detecting turbidness due to a complex of the basic peptide and denatured albumin.
Abstract:
The present invention provides a recombinant Vaccinia virus as a dengue virus vaccine that can be used as a therapeutic or prophylactic agent in the clinic. This recombinant Vaccinia virus is characterized by including: all or part of a cDNA that encodes a non-structural protein from a dengue virus; and an expression promoter.
Abstract:
A method of producing macrophages includes a culture step of culturing hematopoietic progenitor cells in the presence of a TREM2 signal activator.
Abstract:
The invention relates to an antibody which binds to myelin oligodendrocyte glycoprotein (MOG), an antibody fragment thereof, a hybridoma which produces the antibody or the antibody fragment, a nucleic acid containing a nucleotide sequence which encodes the antibody or the antibody fragment, a transformant cell containing a vector containing the nucleic acid, a method for producing the antibody or the antibody fragment, a composition containing the antibody or the antibody fragment and a method for detecting or measuring an antigen that is present in the brain, a method for diagnosing or treating a brain disease, a method for improving the property of an antibody of accumulating in the brain and a method for increasing the amount of an antibody in the brain which use the antibody or the antibody fragment.
Abstract:
Described is a labeling technique which can facilitate the metabolism in the liver after administration to patients without the reduction in the antibody function, thereby reducing accumulation of radionuclides in an organ such as the liver, and a modified antibody containing an IgG antibody and an IgG-binding peptide bound to the IgG antibody. The IgG-binding peptide has an amino acid sequence consisting of 13 to 17 amino acid residues, such as GPDCAYH(Xaa1)GELVWCTFH (SEQ ID NO: 2) wherein Xaa1 represents a lysine residue, a cysteine residue, an aspartic acid residue, a glutamic acid residue, 2-aminosuberic acid, or diaminopropionic acid, and a compound represented by the following formula (II-1) is linked at a position of the lysine residue via a modification linker to the N terminus of the IgG-binding peptide.
Abstract:
A peptide vaccine complexed so that the peptide vaccine can be delivered specifically to the surface of specific immune cells and a method for delivering a peptide vaccine specifically to the surface of specific immune cells. The peptide vaccine is combined with an IgG binding peptide capable of binding to an IgG that is an agonist against molecules on the surface of specific immune cells such as dendritic cells.