Abstract: This application relates to a radio frequency identification (RFID) tag module. In one aspect, the RFID tag module may have a temperature/humidity logging function that can log temperature and humidity inside a box, based on an RFID tag, to stably manage the quality of a product contained in the box. The RFID tag module may be installed in the box in which the product is packed. The RFID tag module may include a temperature/humidity sensor detecting a temperature/humidity inside the box in which the product is packed. The RFID tag module may also include an RFID tag logging the temperature/humidity detected by the temperature/humidity sensor.

Abstract: A portable RFID reader device includes a cross Yagi antenna having good signal reading characteristics regardless of the position of an RFID tag. In embodiments, a portable RFID reader device may include a reader body implemented as a portable type having a handle, and communicating with an RFID tag in a non-contact manner, and a cross Yagi antenna assembly connected to the reader body, and including a cross Yagi antenna transmitting and receiving an RF signal required for communication to and from the RFID tag in a non-contact manner. The cross Yagi antenna may include a plate-shaped first Yagi antenna disposed at an angle of ?45 degrees with respect to a horizontal plane, and a second Yagi antenna disposed at an angle of 45 degrees with respect to the horizontal plane and arranged orthogonally and cross-coupled to the first Yagi antenna.

Abstract: A probe system for real-time quantitative and qualitative analysis of a biomaterial, and a reaction chamber with the probe system, and an analysis method thereof are provided. The probe system, which is included in the reaction chamber having an optically transmissive flat bottom surface and having a test sample accommodated therein, includes a target probe-reporter probe linker accommodated in the reaction chamber and including a target probe, which includes a sequence complementary to a target nucleic acid sequence to be detected, a first fluorophore and a first quencher, and a reporter probe linked to an end of the target probe and including a sequence non-complementary to the target nucleic acid sequence, and a capture probe included in a biochip formed on a bottom surface of the reaction chamber and including a complementary sequence hybridizable with the non-complementary sequence of the reporter probe, a second fluorophore and a second quencher.

Abstract: A method of quantitatively and qualitatively analyzing a biomaterial in real-time, the method comprising preparing a device for detecting a biomaterial, feeding a complex of first and second probes, a forward primer, a reverse primer, a sample comprising deoxynucleotide triphosphate, a polymerase having exonuclease activity, and a sample comprising target genes, and a reaction solution comprising a buffer into the reaction container, performing polymerase chain reaction comprising denaturation of the target genes in the sample, hybridization of the target genes, the complex, and the forward and reverse primers in the sample, and elongation of the primers through the polymerase having exonuclease activity, allowing for elongation of the second probe on the third probe by the polymerase after hybridizing the released second probe and the third probe fixed to the biochip, detecting a first fluorescence signal by the first phosphor and a second fluorescence signal by the second phosphor.

Abstract: A probe system for real-time quantitative and qualitative analysis of a biomaterial, and a reaction chamber with the probe system, and an analysis method thereof are provided. The probe system, which is included in the reaction chamber having an optically transmissive flat bottom surface and having a test sample accommodated therein, includes a target probe-reporter probe linker accommodated in the reaction chamber and including a target probe, which includes a sequence complementary to a target nucleic acid sequence to be detected, a first fluorophore and a first quencher, and a reporter probe linked to an end of the target probe and including a sequence non-complementary to the target nucleic acid sequence, and a capture probe included in a biochip formed on a bottom surface of the reaction chamber and including a complementary sequence hybridizable with the non-complementary sequence of the reporter probe, a second fluorophore and a second quencher.

Abstract: A method of quantitatively and qualitatively analyzing a biomaterial in real-time, the method comprising preparing a device for detecting a biomaterial, feeding a complex of first and second probes, a forward primer, a reverse primer, a sample comprising deoxynucleotide triphosphate, a polymerase having exonuclease activity, and a sample comprising target genes, and a reaction solution comprising a buffer into the reaction container, performing polymerase chain reaction comprising denaturation of the target genes in the sample, hybridization of the target genes, the complex, and the forward and reverse primers in the sample, and elongation of the primers through the polymerase having exonuclease activity, allowing for elongation of the second probe on the third probe by the polymerase after hybridizing the released second probe and the third probe fixed to the biochip, detecting a first fluorescence signal by the first phosphor and a second fluorescence signal by the second phosphor.

Abstract: An apparatus capable of providing location-based data includes a communication unit to transmit data to a server and to receive base location-based data from the server via a communication network, a display unit to display the base location-based data, and a control unit to control the display unit to further display synthesized data including first user location-based data and the base location-based data. A method for providing location-based data includes acquiring user location-based data including location information, acquiring base location-based data including location information, and synthesizing the user location-based data into corresponding region of the base location-based data.

Abstract: The present invention relates to an improved somatotropin composition consisting of somatotropin having in vivo, at least one of lipid-soluble vitamins and at least one of pharmaceutically acceptable lubricants, which improves poor syringeability under cold temperature which has been a defect of the conventional somatotropin formulation using vitamins, and which shows at least the equivalent effect to that of the conventional formulation.

Abstract: An integrated goods and online services vending machine includes an indication module for displaying items and services list and receiving a request by a customer's selection, an advertisement module for displaying various advertisements, a card settlement unit for identifying customer's card and charging the card on requesting, and an electronic control unit (ECU) for integrally controlling the indication module, the advertisement module, and the card settlement unit 130, wherein the ECU requests settlement permission from an authentication organization via public network on the basis of information from the card settlement unit and executes the service request inputted through the indication module if the authentication organization permits a present settlement.

Abstract: The present invention relates to a pharmaceutical compositions which comprises bioactive somatotropin and at least two kinds of lipid-soluble vitamins, and more particularly to a parenterally administered pharmaceutical composition which can solve inconvenience of administering somatotropin and lipid-soluble vitamins respectively and which shows the sustained effect of somatotropin and the synergic effect of somatotropin and lipid-soluble vitamins.

Abstract: The present invention relates to a sustained-release formulation of an animal growth hormone and a process for preparation thereof, comprising a step to produce solid pellets by mixing an animal growth hormone and an excipient in accordance with a direct tabletting method and a step to coat the pellets with a film comprising a biodegradable polymer and a poloxamer. The thus obtained formulation has small initial drug release, and shows a continuous and uniform effect when administered. Further, the formulation of the present invention may be produced economically in a large scale.

Abstract: The present invention relates to a release-controlled implantable composition comprising somatotropin, a bio-compatible wax and a water-soluble polymer. The present composition exhibits superior sustained effect with little side effects, which renders it suitable for long-term administration.