Abstract: A DNA chip favorably employable for detecting a DNA fragment complementary to the oligo- or polynucleotide fixed to the chip is composed of a solid carrier and oligonucleotide or polynucleotide which is fixed to the carrier in the presence of a hydrophilic polymer.

Abstract: A biochemical analysis unit is obtained, which comprises a base plate having spot-shaped regions and has identification information, specific binding substances having been fixed respectively to the spot-shaped regions. A labeled organism-originating substance having identification information is subjected to specific binding to the specific binding substances. A label signal corresponding to a position of the spot-shaped region having thus been labeled selectively is read out to form data for a biochemical analysis. The identification information of the biochemical analysis unit and the identification information of the organism-originating substance are acquired and fed into an analysis apparatus, such that the correspondence relationship between the two pieces of the identification information is clear.

Abstract: A biochemical analysis unit includes a plurality of absorptive regions formed spaced apart from each other by covering a surface of an absorptive substrate made of an absorptive material with a material capable of attenuating radiation energy and/or light energy.

Abstract: A DNA chip favorably employable for detecting a DNA fragment complementary to the oligo- or polynucleotide fixed to the chip is composed of a solid carrier and oligonucleotide or polynucleotide which is fixed to the carrier in the presence of a hydrophilic polymer.

Abstract: A simple and efficient method is proposed for the preparation of a &bgr;-lactam compound such as 1-phenyl-4-ethoxy-2-azetidinone which can be produced by mixing an isocyanate compound such as phenyl isocyanate and a vinyl ether compound such as ethyl vinyl ether and heating the mixture at a moderate temperature under a superatmospheric pressure of up to 12000 atmospheres.

Abstract: A protein dyeing and detecting method includes steps of fixing a protein electrophoresed on a gel on the gel using a fixing solution, dyeing the fixed protein with fluorescent dye for dyeing a protein which has a property of mainly acting on sodium dodecyl sulfide (SDS)-protein complex to dye a protein, irradiating the dyed protein with a stimulating ray and detecting fluorescent light emitted from the protein upon being irradiated to produce a fluorescent image of a protein, the fluorescent dye for dyeing a protein being most effectively stimulated with a stimulating ray having a wavelength between 440 nm to 500 nm or a wavelength between 510 nm to 580 nm and emitting fluorescent light whose peak wavelength ranges from 560 nm to 620 nm or from 600 nm to 660 nm. According to the thus constituted protein dyeing and detecting method, it is possible to produce a fluorescent image of a protein having high sharpness and low background noise.

Abstract: An image reading apparatus includes a first laser stimulating ray source for emitting a laser beam having a wavelength of 633 nm or 635 nm, a second laser stimulating ray source for emitting a laser beam having a wavelength of 470 to 480 nm, a laser beam scanning device for scanning the laser beam, at least one light detector for photoelectrically detecting light released from an image carrier carrying an image, and at least one filter member disposed in front of the light detector and having a plurality of filters for transmitting light of different wavelengths. The thus constituted image reading apparatus can be used for a radiation diagnosis system, an autoradiographic system, an electron microscope detecting system and a radiation diffraction image detecting system using a stimulable phosphor and a fluorescence detecting system and an image can be read with high sensitivity.

Abstract: Disclosed is a novel .beta.-lactam compound, a 7-substituted-2-oxa-7-azabicyclo?3.2.0!heptan-6-one represented by the general formula ##STR1## in which R is an alkyl, cycloalkyl, aryl, halogen-substituted aryl or alkaryl group, having usefulness as an intermediate for the synthesis of various biologically active compounds. The compound can be prepared by the reaction of an isocyanate compound RNCO, R being the same as above, and 2,3-dihydrofuran, preferably, under pressurization up to 2000 atmospheres or higher.

Abstract: A novel and simple method is proposed for the synthetic preparation of an N,N-disubstituted .beta.-ketothioamide compound represented by the general formulaR.sup.1 R.sup.2 N--CS--CH.sub.2 --CO--R.sup.3,in which R.sup.1 and R.sup.2 are each a monovalent hydrocarbon group or each a divalent hydrocarbon group jointly forming a cyclic structure together with the nitrogen atom and R.sup.3 is a hydrogen atom, a monovalent hydrocarbon group or a divalent hydrocarbon group forming a cyclic structure jointly with R.sup.1, R.sup.1 being a divalent hydrocarbon group and R.sup.2 being a monovalent hydrocarbon group. The method comprises:(a) mixing an N,N-disubstituted amide compound represented by the general formulaR.sup.1 R.sup.2 N--CO--R.sup.3,and a bis(trialkylsilyl)thioketene compound represented by the general formula(R.sub.3 Si).sub.2 C.dbd.C.dbd.

Abstract: A chemiluminescent detecting method includes the steps of uniformly irradiating with radiation a stimulable phosphor sheet formed with a stimulable phosphor layer containing a stimulable phosphor which can store an energy of radiation and be stimulated by visible light to emit the energy of radiation in a form of light, thereby storing energy of radiation uniformly therein, selectively labeling a biopolymer with a labeling substance which can produce chemiluminescent light by contact of itself and a chemiluminescent substance, causing the biopolymer labeled with the labeling substance and the chemiluminescent substance to come into contact with each other, and exposing the stimulable phosphor sheet to chemiluminescent light produced by the contact of the biopolymer labeled with the labeling substance and the chemiluminescent substance.

Abstract: Disclosed is a method for the preparation of a .beta.-thiolactam compound, i.e. a 7-substituted-2-oxa-7-azabicyclo [3.2.0]-heptan-6-thione, represented by the general formula ##STR1## in which R is an alkyl or aryl group, having usefulness as an intermediate for the synthesis of various biologically active compounds. The compound can be prepared by the reaction of an isothiocyanate compound R--NCS, R being the same as above, and 2,3-dihydrofuran, preferably, under pressurization up to 2000 atmospheres or higher at an elevated temperature.

Abstract: Disclosed is a novel .beta.-lactam compound, a 7-substituted-2-oxa-7-azabicyclo[3.2.0]heptan-6-one represented by the general formula ##STR1## in which R is an alkyl, cycloalkyl, aryl, halogen-substituted aryl or alkaryl group, having usefulness as an intermediate for the synthesis of various biologically active compounds. The compound can be prepared by the reaction of an isocyanate compound RNCO, R being the same as above, and 2,3-dihydrofuran, preferably, under pressurization up to 2000 atmospheres or higher.

Abstract: There is disclosed a novel thiadiazine, 2,6-bis(disubstituted amino)-4-dialkylthiocarbamoylimino-1,3,5-thiadiazine, and method for preparing same. According to the disclosure a compound useful for a medicine and agricultural chemical can be obtained efficiently by a one-step reaction using inexpensive raw materials.