Abstract: A medical image display apparatus includes the following. A touch operating unit receives a touch input on a display screen of a display which displays a medical image. A display controller moves a movement operation element in response to the touch input to a region including the medical image except for the movement operation element displayed on the display screen.

Abstract: A medical image display apparatus includes the following. A touch operating unit receives a touch input on a display screen of a display which displays a medical image. A display controller moves a movement operation element in response to the touch input to a region including the medical image except for the movement operation element displayed on the display screen.

Abstract: A frequency modulation circuit includes a calibration-operating part which calculates primary calibration values of modulation index at central frequencies of respective ones of n pieces of TF bands which constitute the entire TF range. Interpolation-calculation part performs an interpolation-calculation with respect to the n pieces of primary calibration values and calculates calibration values at intermediate frequencies of central frequencies of neighboring ones of TF bands while calculating calibration values at frequencies at both ends of entire TF range to obtain (n+1) pieces of interpolated calibration values as secondary calibration values. Calibration value supply part supplies one calibration value corresponding to the TF bands set in the TF band setting part from among the primary calibration values or secondary calibration values to a modulation part performing frequency modulation together with calculation based on the supplied calibration value.

Abstract: A frequency modulation circuit includes a calibration-operating part which calculates primary calibration values of modulation index at central frequencies of respective ones of n pieces of TF bands which constitute the entire TF range. Interpolation-calculation part performs an interpolation-calculation with respect to the n pieces of primary calibration values and calculates calibration values at intermediate frequencies of central frequencies of neighboring ones of TF bands while calculating calibration values at frequencies at both ends of entire TF range to obtain (n+1) pieces of interpolated calibration values as secondary calibration values. Calibration value supply part supplies one calibration value corresponding to the TF bands set in the TF band setting part from among the primary calibration values or secondary calibration values to a modulation part performing frequency modulation together with calculation based on the supplied calibration value.

Abstract: An ultrasound diagnostic imaging apparatus includes an ultrasound probe, a display unit, a touch panel and a control unit. The touch panel is disposed in such a way as to be superposed on a display screen of the display unit. The control unit (i) displays a body mark representing a body part of a subject on the display screen, (ii) sets an operation receivable region on the touch panel in such a way as to be suitable for the displayed body mark, (iii) detects a touched point in the operation receivable region and (iv) performs display position setting to control the display unit to display a probe mark representing the ultrasound probe in form according to the detected touched point.

Abstract: A medical image generation apparatus is communicably connected to an information processing apparatus which receives inputting and performs displaying of information regarding a test object. The medical image generation apparatus includes: an image data generation section to generate image data of the examination region of the test object; and a control section to request the information processing apparatus to transmit test-object specifying information for specifying the test object, to receive the test-object specifying information transmitted from the information processing apparatus, to obtain test-object information corresponding to the received test-object specifying information from a predetermined test-object information storage section, and to correlate the obtained test-object information to the image data created by the image data generation section.

Abstract: A DNA synthesis reaction-enhancer comprising at least one kind selected from the group consisting of acidic substances and cationic complexes; a DNA synthesis method in which during a DNA synthesis reaction a reaction is carried out in the presence of the above enhancer by using DNA polymerase; a DNA synthesis reaction composition comprising the above enhancer; a DNA synthesis reaction composition comprising two or more kinds of DNA polymerases each having 3??5? exonuclease activity; a DNA synthesis method in which during a DNA synthesis reaction two or more kinds of DNA polymerases each having 3??5? exonuclease activity are used; a kit for use in in vitro DNA synthesis, comprising two or more kinds of DNA polymerases each having 3??5? exonuclease activity; and a kit for use in in vitro DNA synthesis, wherein the kit comprises the DNA synthesis reaction-enhancer and DNA polymerase.

Abstract: A thermal cycler for incubating reaction mixture, the thermal cycler including:(1) a heat block for holding and heating reaction containers which contain the reaction mixture, the heat block being a double-layered structure of a lower layer heat block and an upper layer heat block; and (2) a thermal control means for controlling a temperature of the lower layer heat block and a temperature of the upper layer heat block independently and respectively and keeping the temperature of the upper layer heat block higher than the temperature of the lower layer heat block while incubating the reaction mixture. Since the thermal cycler prevents the occurrence of the condensation of water or other components of the reaction mixture in the reaction container and the thermal differences based on the installation positions of the reaction containers, the PCR method and the other enzyme reaction can be performed in a good repeatability.

Abstract: There are provided a radiation-proof resin composition that is excellent in mechanical characteristics even after exposure to harsh radiation (with 2.5 MGy), that exhibits a suitable radiation-resistant properties by a small amount of mixed additives, and that can suppress the blooming of the additives, and a radiation-resistant wire/cable. The radiation-resistant resin composition is obtained by adding 0.3 to 1.0 parts by mass of a salicylate-based UV absorber, 0.3 to 5 parts by mass of a benzotriazole-based UV absorber, and 0.3 to 5 parts by mass of a triazine-based UV absorber to 100 parts by mass of a polyolefin-based resin.

Abstract: There are provided a radiation-proof resin composition that is excellent in mechanical characteristics even after exposure to harsh radiation (with 2.5 MGy), that exhibits a suitable radiation-resistant properties by a small amount of mixed additives, and that can suppress the blooming of the additives, and a radiation-resistant wire/cable. The radiation-resistant resin composition is obtained by adding 0.3 to 1.0 parts by mass of a salicylate-based UV absorber, 0.3 to 5 parts by mass of a benzotriazole-based UV absorber, and 0.3 to 5 parts by mass of a triazine-based UV absorber to 100 parts by mass of a polyolefin-based resin.

Abstract: A DNA synthesis reaction-enhancer comprising at least one kind selected from the group consisting of acidic substances and cationic complexes; a DNA synthesis method in which during a DNA synthesis reaction a reaction is carried out in the presence of the above enhancer by using DNA polymerase; a DNA synthesis reaction composition comprising the above enhancer; a DNA synthesis reaction composition comprising two or more kinds of DNA polymerases each having 3??5? exonuclease activity; a DNA synthesis method in which during a DNA synthesis reaction two or more kinds of DNA polymerases each having 3??5? exonuclease activity are used; a kit for use in in vitro DNA synthesis, comprising two or more kinds of DNA polymerases each having 3??5? exonuclease activity; and a kit for use in in vitro DNA synthesis, wherein the kit comprises the DNA synthesis reaction-enhancer and DNA polymerase.

Abstract: A DNA synthesis reaction-enhancer comprising at least one kind selected from the group consisting of acidic substances and cationic complexes; a DNA synthesis method in which during a DNA synthesis reaction a reaction is carried out in the presence of the above enhancer by using DNA polymerase; a DNA synthesis reaction composition comprising the above enhancer; a DNA synthesis reaction composition comprising two or more kinds of DNA polymerases each having 3??5? exonuclease activity; a DNA synthesis method in which during a DNA synthesis reaction two or more kinds of DNA polymerases each having 3??5? exonuclease activity are used; a kit for use in in vitro DNA synthesis, comprising two or more kinds of DNA polymerases each having 3??5? exonuclease activity; and a kit for use in in vitro DNA synthesis, wherein the kit comprises the DNA synthesis reaction-enhancer and DNA polymerase.

Abstract: In the case where a template nucleic acid has sequences substantially the same as each other, a primer is designed in a region between these sequences so as to give a product in a ladder structure in which a target region is polymerized in a single sequence via the same sequences in the ICAN reaction. By using a chimeric oligonucleotide primer and a ladder-forming oligonucleotide primer containing a specific base sequence, an amplification product having a ladder structure can be positively formed and thus the sensitivity, amplification efficiency and reaction speed in the ICAN reaction can be elevated.

Abstract: A method of analyzing, in chromosomal DNA having a retroviral vector incorporated therein, DNA region derived from chromosome which is adjacent to the vector, characterized in that a primer extension reaction and a nucleic acid amplification reaction are carried out in the presence of a compound capable of lowering the Tm value of double stranded nucleic acid. There are further provided a kit and buffer for use in this method.

Abstract: The present invention provides an electric resistance welded steel pipe for a hollow stabilizer excellent in workability, which steel pipe contains, in mass, 0.20 to 0.35% of C, 0.10 to 0.50% of Si, 0.30 to 1.00% of Mn, 0.01 to 0.10% of Al, 0.10 to 1.00% of Cr, 0.005 to 1.00% of Mo, 0.001 to 0.02% of Ti, 0.0005 to 0.0050% of B and 0.0010 to 0.0100% of N, satisfying the expression N/14<Ti/47.9, the balance consisting of Fe and unavoidable impurities and further has an ideal critical diameter (Di) being 1.0 (in) or more, an n-value in the axial direction of the steel pipe being 0.12 or more, a difference in hardness between the electric resistance welded seam portion and the base steel being Hv 30 or less, an average grain size of ferrite being 3 to 40 ?m, an area percentage of the ferritic crystal grains having the aspect ratios of 0.5 to 3.0 being 90% or more in the entire ferrite phase, and having an average grain size of 20 ?m or less in the second phase.

Abstract: A convenient and effective method for amplifying a nucleic acid sequence characterized by effecting a DNA synthesis reaction in the presence of chimeric oligonucleotide primers; a method for supplying a large amount of DNA amplification fragments; an effective method for amplifying a nucleic acid sequence by combining the above method with another nucleic acid sequence amplification method; a method for detecting a nucleic acid sequence for detecting or quantitating a microorganism such as a virus, a bacterium, a fungus or a yeast; and a method for detecting a DNA amplification fragment obtained by the above method in situ.

Abstract: A support for ligand immobilization coated with a polyanion which has been activated beforehand.

Abstract: A convenient and effective method for amplifying a nucleic acid sequence characterized by effecting a DNA synthesis reaction in the presence of chimeric oligonucleotide primers; a method for supplying a large amount of DNA amplification fragments; an effective method for amplifying a nucleic acid sequence by combining the above method with another nucleic acid sequence amplification method; a method for detecting a nucleic acid sequence for detecting or quantitating a microorganism such as a virus, a bacterium, a fungus or a yeast; and a method for detecting a DNA amplification fragment obtained by the above method in situ.

Abstract: A convenient and effective method for amplifying a nucleic acid sequence characterized by effecting a DNA synthesis reaction in the presence of chimeric oligonucleotide primers; a method for supplying a large amount of DNA amplification fragments; an effective method for amplifying a nucleic acid sequence by combining the above method with another nucleic acid sequence amplification method; a method for detecting a nucleic acid sequence for detecting or quantitating a microorganism such as a virus, a bacterium, a fungus or a yeast; and a method for detecting a DNA amplification fragment obtained by the above method in situ.

Abstract: A nucleic acid, which is provided in a large amount through a nucleic acid amplification reaction with the use of chimeric oligonucleotide primers, is constructed in a state of containing a modified deoxyribonucleotide for immobilizing the nucleic acid to a solid phase and then immobilized to a solid phase at a high efficiency, thereby giving an immobilized nucleic acid product with excellent qualities.