Abstract: A vehicle control system includes: an entry/exit management device including a first processor including hardware, the first processor being configured to detect that a user of a vehicle enters or leaves a facility, and output a first signal indicating user's entering the facility and a second signal indicating user's leaving the facility, to a server; and the server comprising a second processor comprising hardware, the second processor being configured to output to the vehicle a third signal for deactivating a smart key function of the vehicle when acquiring the first signal and prohibit unlocking of a door of the vehicle performed by wireless communication, and output to the vehicle a fourth signal for setting the smart key function of the vehicle when acquiring the second signal and permit unlocking of the door of the vehicle performed by wireless communication.

Abstract: A blood purification apparatus that includes a blood circuit including an arterial blood circuit and a venous blood circuit and that allows a patient's blood to extracorporeally circulate, with a blood purifier that is interposed between the arterial blood circuit and the venous blood circuit and purifies; a dialysate temporary chamber that temporarily stores dialysate received from a dialysate storage supported by a supporting unit; a substitution-fluid temporary chamber that temporarily stores substitution fluid received from a substitution-fluid storage supported by the supporting unit; a first dialysate introduction line through which the dialysate in the dialysate storage flows into the dialysate temporary chamber; and a substitution line through which the substitution fluid in the substitution-fluid storage flows into the substitution-fluid temporary chamber.

Abstract: The present invention relates to a binder composition for a non-aqueous electrolyte battery, which is characterized by containing (A) polyvinyl alcohol, (B) at least one selected from a copolymer of vinyl alcohol and ethylenically unsaturated carboxylic acid and a neutralized salt of the copolymer and (C) at least one selected from an amino acid, a carboxylic acid-containing polymer and a polyamine; and a binder aqueous solution for a non-aqueous electrolyte battery, a slurry composition for a non-aqueous electrolyte battery, an electrode for a non-aqueous electrolyte battery, and a non-aqueous electrolyte battery, each containing the binder composition; and others.

Abstract: Disclosed is a novel means for accurate qualitative and quantitative analyses for each N-glycosylation site. The method of analyzing N-linked sugar chain(s) of glycoprotein according to the present invention comprises: treating a part of a glycopeptide-containing sample to be analyzed with endo-?-N-acetylglucosaminidases to cleave off sugar chains while leaving one GlcNAc of the chitobiose core on the Asn at the N-glycosylation site; subjecting the obtained sugar chain-cleaved sample to preliminary liquid chromatography/mass spectrometry; predicting the retention time of the glycopeptide of interest and the mass-to-charge ratio (m/z) of the precursor ion in main analysis based on the results of the preliminary liquid chromatography/mass spectrometry; and carrying out the main analysis. By this method, the binding sites and structures of N-linked sugar chains in a glycoprotein can be analyzed.

Abstract: The invention relates to a pancreatic cancer determination marker, a pancreatic cancer determination method, a method for acquiring data for determining a pancreatic cancer, a pancreatic cancer determination kit, and the like.

Abstract: Disclosed is a novel means for accurate qualitative and quantitative analyses for each N-glycosylation site. The method of analyzing N-linked sugar chain(s) of glycoprotein according to the present invention comprises: treating a part of a glycopeptide-containing sample to be analyzed with endo-?-N-acetylglucosaminidases to cleave off sugar chains while leaving one GlcNAc of the chitobiose core on the Asn at the N-glycosylation site; subjecting the obtained sugar chain-cleaved sample to preliminary liquid chromatography/mass spectrometry; predicting the retention time of the glycopeptide of interest and the mass-to-charge ratio (m/z) of the precursor ion in main analysis based on the results of the preliminary liquid chromatography/mass spectrometry; and carrying out the main analysis. By this method, the binding sites and structures of N-linked sugar chains in a glycoprotein can be analyzed.

Abstract: The present invention pertains to: a non aqueous electrolyte battery binder composition containing a polyamine and a neutralized salt of an ?-olefin-maleic acid copolymer obtained through copolymerization of an ?-olefin and maleic acid; and a non aqueous electrolyte battery slurry composition, a non aqueous electrolyte battery negative electrode, and a non aqueous electrolyte battery, etc., using the non aqueous electrolyte battery binder composition.

Abstract: The present invention pertains to a slurry composition for non aqueous electrolyte battery electrodes that includes a binder composition, an active material, and a solvent, in which the active material is a lithium-containing metal oxide, the binder composition contains a neutralized salt of an ?-olefin-maleic acid copolymer in which an ?-olefin and a maleic acid are copolymerized, and the degree of neutralization for carboxylic acid generated from the maleic acid in the copolymer is from 0.3 to 1.0. The present invention further pertains to a non aqueous electrolyte battery positive electrode and a non aqueous electrolyte battery using the slurry composition for non aqueous electrolyte battery electrodes.

Abstract: The present invention relates to a binder composition for a non-aqueous electrolyte battery, which is characterized by containing (A) polyvinyl alcohol, (B) at least one selected from a copolymer of vinyl alcohol and ethylenically unsaturated carboxylic acid and a neutralized salt of the copolymer and (C) at least one selected from an amino acid, a carboxylic acid-containing polymer and a polyamine; and a binder aqueous solution for a non-aqueous electrolyte battery, a slurry composition for a non-aqueous electrolyte battery, an electrode for a non-aqueous electrolyte battery, and a non-aqueous electrolyte battery, each containing the binder composition; and others.

Abstract: In a liquid chromatograph mass spectrometer (LC/MS) for performing mass spectrometry of fractionated samples prepared with a multi-dimensional LC or similar LC with high separatory capability, fractionated sample useful information which shows the degree of usefulness of various substances with respect to retention time is prepared from prior information which includes, for example, elution characteristics in the LC depending on the kind of column or other factors or the degree of ease of ionization in the MS. During a measurement, the preparative separation of an eluate and the preparation of fractionated samples are not performed within a period of time which has been judged to be useless based on the fractionated sample useful information. By selecting fractionated samples at each dimension of the multi-dimensional LC, the number of fractionated samples to be eventually subjected to mass spectrometry can be significantly reduced.

Abstract: The present invention pertains to: a non aqueous electrolyte battery binder composition containing a polyamine and a neutralized salt of an ?-olefin-maleic acid copolymer obtained through copolymerization of an ?-olefin and maleic acid; and a non aqueous electrolyte battery slurry composition, a non aqueous electrolyte battery negative electrode, and a non aqueous electrolyte battery, etc., using the non aqueous electrolyte battery binder composition.

Abstract: The present invention pertains to a non aqueous electrolyte battery binder composition containing a polyether and a neutralized salt of an ?-olefin-maleic acid copolymer obtained through copolymerization of an ?-olefin and maleic acid; and a non aqueous electrolyte battery slurry composition, a non aqueous electrolyte battery negative electrode, and a non aqueous electrolyte battery using the non aqueous electrolyte battery binder composition.

Abstract: The present invention pertains to a slurry composition for non aqueous electrolyte battery electrodes that includes a binder composition, an active material, and a solvent, in which the active material is a lithium-containing metal oxide, the binder composition contains a neutralized salt of an ?-olefin-maleic acid copolymer in which an ?-olefin and a maleic acid are copolymerized, and the degree of neutralization for carboxylic acid generated from the maleic acid in the copolymer is from 0.3 to 1.0. The present invention further pertains to a non aqueous electrolyte battery positive electrode and a non aqueous electrolyte battery using the slurry composition for non aqueous electrolyte battery electrodes.

Abstract: A peptide is cleaved at various bonding sites into oligopeptides or similar fragments by digestion using proteinase K (S3). The obtained fragments are separated according to their kinds by reversed-phase chromatography and fractionated (S4), and each fragment is subjected to mass spectrometry to determine its mass (S6). For each peptide fragment, an amino-acid composition is calculated from the measured mass, and amino-acid sequence candidates are deduced from that composition. The amino-acid sequence candidates of the other peptide fragments are searched for a fragment having an overlapping portion available for combining two peptide fragments to obtain amino-acid sequence candidates of the original peptide (S7). The masses of the amino-acid sequence candidates are compared with a measured mass derived from a result of mass spectrometry of the original peptide to select a correct sequence (S6 and S8).

Abstract: In a liquid chromatograph mass spectrometer (LC/MS) for performing mass spectrometry of fractionated samples prepared with a multi-dimensional LC or similar LC with high separatory capability, fractionated sample useful information which shows the degree of usefulness of various substances with respect to retention time is prepared from prior information which includes, for example, elution characteristics in the LC depending on the kind of column or other factors or the degree of ease of ionization in the MS. During a measurement, the preparative separation of an eluate and the preparation of fractionated samples are not performed within a period of time which has been judged to be useless based on the fractionated sample useful information. By selecting fractionated samples at each dimension of the multi-dimensional LC, the number of fractionated samples to be eventually subjected to mass spectrometry can be significantly reduced.

Abstract: An opening/closing body operation device for operating an opening/closing body, which swings up and down, so as to open and close, has a driving unit, a slider which is moved up and down by the driving force from the driving unit and is linked to the opening/closing body and a guide member having the slider slidably disposed in the interior. The slider includes a main slider body, a sliding member that slides on the guide member, and an elastic member between the main slider body and the sliding member to support the load applied to the slider when the opening/closing body is opened or closed. The slider has a deformation allowance space for allowing elastic deformation of the elastic member caused when the slider is pressed into the guide member. Thus, the load applied to the slider to open or close the opening/closing body is reliably supported.

Abstract: A peptide is cleaved at various bonding sites into oligopeptides or similar fragments by digestion using proteinase K (S3). The obtained fragments are separated according to their kinds by reversed-phase chromatography and fractionated (S4), and each fragment is subjected to mass spectrometry to determine its mass (S6). For each peptide fragment, an amino-acid composition is calculated from the measured mass, and amino-acid sequence candidates are deduced from that composition. The amino-acid sequence candidates of the other peptide fragments are searched for a fragment having an overlapping portion available for combining two peptide fragments to obtain amino-acid sequence candidates of the original peptide (S7). The masses of the amino-acid sequence candidates are compared with a measured mass derived from a result of mass spectrometry of the original peptide to select a correct sequence (S6 and S8).