Abstract: A multicolor fluorescence detection type electrophoresis apparatus comprises an electrophoretic device having migration lanes in which fragment groups specifically labeled by fluorophores of different light emission peak wavelengths are mixed, added, and migrated. It identifies and detects the fragment groups. It uses laser beams of different wavelengths for exciting the fluorophores in the migration lanes. The laser beams are irradiated to separate positions on the migration lanes for detection of a few kinds of fluorophores at irradiation positions. For the purpose, multicolor optical filters are arranged near the irradiation positions to identify and detect lights emitted from the fluorophores excited by wavelength at every irradiation position.

Abstract: In a fluorescence detection type electrophoresis apparatus, comprising an electrophoresis separation gel plate (2, 102, 205), an excitation laser beam source (3, 201, 201) for emitting fluorescent light, and a fluorescent light detector (9, 109, 212) for detecting the emitted fluorescent light, a fluorescent light images are divided into a plurality of virtual images by an image divider (5, 7.sub.2, 104, 105, 209) and at the same time, the lights corresponding to the individual divided images are wavelength-selected by bandpass filters (8, 8.sub.3, 107, 108, 120, 227-230), thereby providing highly accurate, sensitive separation and detection of DNA fragments and the like and determination of base sequence of DNA and the like.

Abstract: In the instrument for determination of the base sequence of the present invention, the ionic strength of a buffer solution in a gel is made lower at a detection part than in a region from the detection part towards a negative electrode. Therefore, at the detection part, the electric field intensity can be increased, resulting in a higher migration speed, and hence the electrophoretic pattern can be extended, so that the distance between two adjacent electrophoretic bands can be elongated.Consequently, according to the present invention, the slit width can be narrowed relatively to the electrophoretic pattern without actually narrowing the slit width, and the resolving power can be enhanced without lowering the detection sensitivity.

Abstract: An instrument for determination of the base sequence of deoxyribonucleic acid (DNA) which is designed to dectect DNA fragments in course of gel electrophoresis in real time to determine the base sequence of DNA, and comprises a gel electrophoretic panel part wherein DNA fragments labeled with a radioisotope are supplied to four places in a gel for four kinds of complementary strand synthesis reaction systems, respectively, and subjected to electrophoresis to form an electrophoretic pattern of the DNA fragments, and a detection part for detecting the electrophoretic pattern of the DNA fragments provided at a predetermined position in said gel electrophoretic panel part so as to have a position resolving power in a direction perpendicular to the direction of electrophoretic migration of the DNA fragments, and which instrument has a means for making the temperature of the gel in the vicinity of the detection part for detecting the electrophoretic pattern of the DNA fragments higher than that on the DNA fragment

Abstract: A method of controlling culture wherein cells are aerobically cultured to produce metabolite is characterized by adding substrate and/or inducer to the culture broth, judging the endpoint of the growth of the cells and/or the production of the metabolite or terminating the culture under the guidance of a change in the ratio of the first parameter based on the amount of carbon dioxide evolved by the cell culture to the second parameter based on the amount of oxygen consumed by the cell culture. The ratio is a respiratory quotient, for instance.

Abstract: A method for detecting a polymerization rate, wherein a polymer composition in a polymerization reaction process is sampled out and can be measured, and is separated into a volatile component and a non-volatile component, and the polymerization rate of the polymer composition is determined using the measured amount of the volatile component and/or non-volatile component, and also possibly the measured amount of the sample. Such method is best suited for detecting the rate of polymerization of polymer compositions. This enables proper quality control of the polymer composition in the polymerization reaction process.

Abstract: Continuous bulk polymerization of thermoplastic resins is carried out by using a horizontal continuous polymerizer comprising a cylindrical body, one or more shafts having the stirring elements and disposed in said body, a material inlet provided at an end of said body in its longitudinal direction, and a material drawing means and an outlet provided at the other end of said body. A monomer is evaporated from a polymerization solution while controlling the pressure in said polymerizer at a predetermined level and, concurrently with this, a monomer is directly sprayed to the free surface of the polymerization solution in the polymerizer from several locations of said polymerizer in its longitudinal direction, whereby to eliminate the heat of polymerization reaction and the heat of stirring to allow progress of the polymerization reaction under a predetermined temperature condition.