Abstract:
There is provided a real-time PCR assay capable of measuring the number of lactobacillus present in an oral cavity, in a short time. The object can be solved by a method for measuring the number of oral lactobacillus using a combination of a forward primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 1 to 4 and a reverse primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 5 to 7; and a probe for measuring the number of oral lactobacillus, comprising a oligonucleotide part of at least 10 sequential bases in the base sequence any one of SEQ ID NO: 8 to 15.
Abstract translation:提供了能够在短时间内测量存在于口腔中的乳杆菌数量的实时PCR测定。 该目的可以通过使用包含SEQ ID NO:1至4中任一个的碱基序列中的至少15个连续碱基的寡核苷酸部分的正向引物和反向引物的方法来测量口服乳酸杆菌的数量的方法 包含SEQ ID NO:5至7中任一个的碱基序列中至少15个连续碱基的寡核苷酸部分; 以及用于测量口服乳杆菌数量的探针,其包含SEQ ID NO:8至15中任一个的碱基序列中至少10个连续碱基的寡核苷酸部分。
Abstract:
There is provided a real time PCR assay capable of calculating a ratio of the number of mutans streptococci to the number of oral streptococci present in an oral cavity, in a short time.The object can be solved by a method for measuring the number of oral streptococci using the combination of a forward primer comprising a primer oligonucleotide part of at least 15 sequential bases in the base sequence of SEQ ID NO: 1 and a reverse primer comprising a probe oligonucleotide part of at least 15 sequential bases in the base sequence of SEQ ID NO: 2; and a probe for measuring the number of oral streptococci, comprising a nucleotide part consisting of at least 10 sequential bases in the base sequence of SEQ ID NO: 3 or 4.
Abstract translation:提供了能够在短时间内计算变形链球菌数目与口腔中存在的口服链球菌数目的比率的实时PCR测定法。 该目的可以通过使用包含SEQ ID NO:1的碱基序列中的至少15个连续碱基的引物寡核苷酸部分的正向引物和包含探针的反向引物的组合来测量口服链球菌数的方法来解决 SEQ ID NO:2的碱基序列中至少15个连续碱基的寡核苷酸部分; 以及用于测量口服链球菌数目的探针,其包含由SEQ ID NO:3或4的碱基序列中的至少10个连续碱基组成的核苷酸部分。
Abstract:
According to one aspect of the present invention, it is possible to sufficiently perform the discharging of charge without lowering the light emitting efficiency of an organic EL device and hence, the device can exhibit the light emitting efficiency higher than a conventional organic EL device and, at the same time, can prevent the degradation of the device. As an organic EL device to which the present invention is applied, on a glass transparent substrate, a transparent electrode, a hole injection layer and a hole transport layer which function as a hole transport function layer, a light emitting layer, an electron transport function layer, and a metal electrode are formed sequentially, and a drive power sources are connected to the transparent electrode and the metal electrode. Further, from the drive power source, as an applying voltage, a voltage which is obtained by overlapping any one of a sine wave, a pulse wave, a triangle wave and a sawtooth wave having two cycles or more to a drive signal or a voltage which is obtained by overlapping a sine wave having two cycles or more to the drive signal is supplied.
Abstract:
In the step of curing a resin for bonding a TFT substrate and a counter substrate each having an alignment film that has been optically aligned by using UV-light, damage to the alignment film due to the UV-light can be prevented without using a light shielding mask. A UV-light absorption layer is formed between each black matrix on the counter substrate. The TFT and counter substrates are sealed at their periphery by a resin that is cured by UV-light radiated from the counter substrate side. Since the absorption layer has a high absorbability to UV-light at a wavelength of 300 nm or less that degrades the alignment film, damage to the alignment film due to the UV-light for curing the resin can be prevented. Thus, provision of a light shielding mask for shielding the UV-light for the display region can be saved.
Abstract:
Provided is a slush molding material which exhibits excellent low-temperature meltability and heat resistance and which can yield a molded product having excellent tensile strength and elongation. The present invention is urethane resin particles (D1) comprising a urethane or urethane-urea resin (U1) that has residues (j) bonded thereto covalently, said residues (j) being residues derived from an at least trivalent aromatic polycarboxylic acid by removing hydroxyl groups, or urethane resin particles (D2) comprising a urethane resin composition (S2) which comprises both a urethane or urethane-urea resin (U2) and a compound (E) that has a residue (j) derived from an at least trivalent aromatic polycarboxylic acid by removing hydroxyl groups, said compound (E) being represented by general formula (1), wherein the residues (j) are linked respectively to urethane or urea groups (u) of the resin (U1) or (U2) by hydrogen bonds.
Abstract:
A liquid crystal display device includes: a pair of substrates at least one of which is transparent; a liquid crystal layer disposed between the pair of substrates; an electrode group formed on at least one substrate of the pair of substrates, for applying an electric field to the liquid crystal layer; a plurality of active elements connected to the electrode group; and a liquid crystal alignment film disposed on at least one substrate of the pair of substrates, in which the liquid crystal alignment film, which is formed by a photo-alignment process, contains polyimide formed using tetracarboxylic acid dianhydride and/or diamine each having a specific chemical structure.
Abstract:
Disclosed is a manufacturing method of a liquid crystal display device which is a manufacturing method of a liquid crystal display device including a liquid crystal alignment film to which an alignment regulating force is imparted by a photo-alignment treatment, including: a film forming step of forming a film containing a polymer whose main chain is cleaved by irradiation with light; a photo-alignment step of imparting an alignment regulating force to the film formed in the film forming step by irradiation of the film with light in an atmosphere of a temperature lower than 100° C.; and a removing step of removing a low-molecular weight component generated by cleaving the main chain of the polymer through the light irradiation after the light irradiation. Also disclosed is a liquid crystal display device manufactured by the manufacturing method.
Abstract:
In the step of curing a resin for bonding a TFT substrate and a counter substrate each having an alignment film that has been optically aligned by using UV-light, damage to the alignment film due to the UV-light can be prevented without using a light shielding mask. A UV-light absorption layer is formed between each black matrix on the counter substrate. The TFT and the counter substrates are sealed at their periphery by a resin that is cured by UV-light radiated from the counter substrate side. Since the absorption layer has a high absorbability to UV-light at a wavelength of 300 nm or less that degrades the alignment film, damage to the alignment film due to the UV-light for curing the resin can be prevented. Thus, provision of a light shielding mask for shielding the UV-light for the display region can be saved.
Abstract:
A method of manufacturing an organic EL display device that includes an element substrate on which a first organic luminescent material and a second organic luminescent material are formed, includes forming the first organic luminescent material by dripping the first organic luminescent material from an inkjet nozzle on the element substrate while relatively moving the inkjet nozzle and the element substrate in a first direction, and forming the second organic luminescent material by dripping the second organic luminescent material from an inkjet nozzle on the element substrate while relatively moving the inkjet nozzle and the element substrate in a direction perpendicular to the first direction.
Abstract:
There is provided a real-time PCR assay capable of measuring the number of lactobacillus present in an oral cavity, in a short time. The object can be solved by a method for measuring the number of oral lactobacillus using a combination of a forward primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 1 to 4 and a reverse primer comprising a oligonucleotide part of at least 15 sequential bases in the base sequence any one of SEQ ID NO: 5 to 7; and a probe for measuring the number of oral lactobacillus, comprising a oligonucleotide part of at least 10 sequential bases in the base sequence any one of SEQ ID NO: 8 to 15.
Abstract translation:提供了能够在短时间内测量存在于口腔中的乳杆菌数量的实时PCR测定。 该目的可以通过使用包含SEQ ID NO:1至4中任一个的碱基序列中的至少15个连续碱基的寡核苷酸部分的正向引物和反向引物的方法来测量口服乳酸杆菌的数量的方法 包含SEQ ID NO:5至7中任一个的碱基序列中至少15个连续碱基的寡核苷酸部分; 以及用于测量口服乳杆菌数量的探针,其包含SEQ ID NO:8至15中任一个的碱基序列中至少10个连续碱基的寡核苷酸部分。