• 산업경영시스템학회지
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• 제19권39호
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• pp.27-36
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• 1996

The objective of this paper is to outline an integrated cellular manufacturing system (ICMS) which integrates process planning and scheduling in the cellular manufacturing environment. It combines design systems with manufacturing systems in batch production. Furthermore, it is developed to overcome the difficulties that exist in the current manufacturing practices.

• 한국전자파학회논문지
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• 제12권7호
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• pp.1037-1047
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• 2001

본 논문에서는 역방향 링크상의 전파 음영 채널에서 불완전 전력제어 및 불완전 섹터화를 고려하여 DS/CDMA 계층 셀룰라 시스템의 용량을 분석한다. 실제 시스템에서는 이론과는 달리 완전한 전력제어가 되지 않기 때문에 불완전 전력제어, 불완전 섹터화 및 처리이득, 매크로셀의 사용자 수와 같은 파라미터를 고려하여 시스템의 용량 변화를 유도하였다. 해석한 결과, 전력제어 및 섹터화가 불완전 할수록, 매크로셀과 마이크로셀의 전력비가 커질수록, 처리이득이 작을수록, 마이크로셀의 사용자 수가 감소할수록 DS/CDMA 계층 셀룰라 시스템의 용량은 감소하였다. 또한, 계층셀 구조가 단일 매크로셀 구조에 비해 1.54 배에서 3.89 배로 사용자 용량을 증가시킬 수 있음을 보였다.

• 한국미생물·생명공학회지
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• 제49권4호
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• pp.478-484
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• 2021

Cellular resources including transcriptional and translational machineries in bacteria are limited, yet microorganisms depend upon them to maximize cellular fitness. Bacteria have evolved strategies for using resources economically. Regulatory networks for the gene expression system enable the cell to synthesize proteins only when necessary. At the same time, regulatory interactions enable the cell to limit losses when the system cannot make a cellular profit due to fake substrates. Also, the architecture of the gene expression flow can be advantageous for clustering functionally related products, thus resulting in effective interactions among molecules. In addition, cellular systems modulate the investment of proteomes, depending upon nutrient qualities, and fast-growing cells spend more resources on the synthesis of ribosomes, whereas nonribosomal proteins are synthesized in nutrient-limited conditions. A deeper understanding of cellular mechanisms underlying the optimal allocation of cellular resources can be used for biotechnological purposes, such as designing complex genetic circuits and constructing microbial cell factories.

• 한국콘크리트학회:학술대회논문집
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• 한국콘크리트학회 1999년도 봄 학술발표회 논문집(I)
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• pp.825-830
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• 1999

The purpose of this study is to improve overall performance of prefoamed lightweight cellular concrete for On-Dol system floor. This study includes 4 sections as follows. \circled1 Analysis of the structural characteristics of On-Dol System focusing on the lightweight cellular concrete insulation layer. \circled2 Establishment of the mixing design equations. \circled3 Development of some admixtures used with foaming agent. \circled4 Improvement of the equipment for onsite production. This study has proven that, compared with the current existing one, the newly developed lightweight cellular concrete has been reduced the usage of cement by 20% and the cracks caused by cement drying shrinkage up to 80% but has shown the increased compression strength by 20% at 7 days curing period. The volume contraction of freshly prepared cellular concrete by the loss of foam was hardly found in newly developed lightweight cellular concrete.

• Molecules and Cells
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• 제27권3호
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• pp.337-343
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• 2009

We developed a novel on-chip activity assay using protein arrays for quantitative and rapid analysis of transglutaminase activity in mammalian cells. Transglutaminases are a family of $Ca^{2+}$-dependent enzymes involved in cell regulation as well as human diseases such as neurodegenerative disorders, inflammatory diseases and tumor progression. We fabricated the protein arrays by immobilizing N,N'-dimethylcasein (a substrate) on the amine surface of the arrays. We initiated transamidating reaction on the protein arrays and determined the transglutaminase activity by analyzing the fluorescence intensity of biotinylated casein. The on-chip transglutaminase activity assay was proved to be much more sensitive than the $[^3H]putrescine$-incorporation assay. We successfully applied the on-chip assay to a rapid and quantitative analysis of the transglutaminase activity in all-trans retinoic acid-treated NIH 3T3 and SH-SY5Y cells. In addition, the on-chip transglutaminase activity assay was sufficiently sensitive to determine the transglutaminase activity in eleven mammalian cell lines. Thus, this novel on-chip transglutaminase activity assay was confirmed to be a sensitive and high-throughput approach to investigating the roles of transglutaminase in cellular signaling, and, moreover, it is likely to have a strong potential for monitoring human diseases.

• 한국통신학회논문지
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• 제25권4A호
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• pp.481-488
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• 2000

The demands for mobile communication service are growing rapidly. In heavily populated areas, cell split is unavoidable to increase the capacity of the cellular system. Cell splitting makes a cellular system to have mixed cell sizes. For cell planning, it is necessary to analyze the reverse link capacity of a CDMA cellular system with mixed cell sizes. In this paper, we propose a method to calculate the reverse link capacity of a CDMA cellular system with mixed cell sizes. When a macro cell is split into three micro cells, as an example, we calculate the reverse link capacities for the three micro cells and the neighboring macro cells. The results show that as the radius of a micro cell decreases, the reverse link capacity of the micro cell increases, while those of the neighboring macro cells decrease.

• 한국미생물·생명공학회지
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• 제23권5호
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• pp.513-518
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• 1995

To evaluate bile salt-tolerance of lactic acid bacteria (LAB, Lactobacillus acidophilus ATCC 4356, Lactobacillus casei IFO 3533, Streptococcus thermnophilus KCTC 2185, Lactobacillus lactis ATCC 4797, and Lactobacillus bulgaricus ATCC 11842), We investigated the survivals, acid production and $\beta $-galactosidase activity of LAB under anaerobic broth system. Cellular permeability of LAB and their cellular retention of $\beta $-galactosidase were also examined in the same system. Although the growth of LAB was slightly suppressed by 0.3% bile salt, they showed normal growth curve. Streptococcus thermophilus KCTC 2185 was significantly more resistant to bile salt than the others. The $\beta $-galactosidase activity from Streptococcus thermophilus KCTC 2185 and Lactobacillus bulgaricus ATCC 11842 and their cellular retention of $\beta $-galactosidase decreased by 0.3% bile salt. The cellular permeability of LAB in the presence of bile salt increased significantly.

• 전자공학회논문지S
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• 제35S권3호
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• pp.39-46
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• 1998

In the FDMA and TDMA Cellular Systems, call blocking rise when frewquence slots andtime slots are used to ther users. Otherwise, in the CDMA cellular systems, call locking arises when interference level is above 10dB according to call of other users. System capacity is defined to be Erlang capacity that is the number of users when CDMA blocking probability is 1% or 2%. Users number corresponded channel number of AMPS and TDMA cellular systems. In this paper, we proposed new reuse-fraction using square of interference poser and obtained Erlang capacity for reverse link of CDMA cellular system with bit rate $R_{b}$, 9.6kbps and 14.4kbps. As a results, Erlange capacity of CDMA system have more 20.7 and 5.5 times than AMPS and TDMA system and have more form 1 to 4 Erlang thatn Viterbi and Padovani obtaned.d.

• 제어로봇시스템학회:학술대회논문집
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• 제어로봇시스템학회 2003년도 ICCAS
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• pp.2451-2456
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• 2003

In biological cell manipulation, manual thrust or penetration of an injection pipette into an egg is currently performed by a skilled operator, relying only on visual feedback information. Massive load of various micro injection of either genes, fluid or cells in the postgenomic era calls a more reliable and automatic micro injection system that can test hundreds of genes or cell types at a single experiment. We initiated to study cellular force sensing in zebrafish eggs as the first step for the development of a more controllable micro injection system by any inexperienced operator. Zebrafish eggs at different developmental stages were collected and an integrated biomanipulation system was employed to measure cellular force during penetrating the egg envelope, the chorion. First of all, the biomanipulation system integrated with cellular force sensing instrument is implemented to measure the penetration force of cell membranes and characterize mechanical properties of zebrafish embryo cells. Furthermore, implementation of cellular force sensing system and calibration are presented. Finally, the cellular force sensing of penetrating cell membranes at each developmental stages was experimentally performed. The results demonstrated that the biomanipulation system with force sensing capability can measure cellular force at real-time while the injection operation is undergoing. The magnitude of the measured force was in the range of several hundreds of uN. The precise real-time measurement should provide the first step forwards for the development of an automatic and reliable injection system of various materials into biological cells.

• 한국통신학회논문지
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• 제33권8A호
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• pp.829-837
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• 2008

멀티미디어 데이터의 전송영역 확장을 위한 기술로 고정 릴레이 기반 셀룰러 시스템에 대한 관심이 지속적으로 증가하고 있다. 고정 릴레이 기반 셀룰러 시스템에서 릴레이를 추가함으로 생기는 셀 간 또는 섹터 간 간섭은 기지국과 단말기 또는 릴레이와 단말이 사이의 높은 링크성능을 보장하지 못하여 성능저하를 가져올 수 있기 때문에 간섭을 회피하기 위한 자원할당은 매우 중요하다. 본 논문에서는 리피터 중계기를 이용한 셀룰러 시스템과 릴레이를 이용한 셀룰러 시스템의 성능을 비교하여 릴레이 중계기를 이용할 때 셀 커버리지 확장을 비교하고자 한다. 비교를 위해 셀룰러 시스템에 고정 릴레이를 설치할 때 셀 간과 섹터 간 간섭을 피하기 위하여 리피터 중계기를 사용하는 경우의 자원할당과는 다른 자원 할당 방법을 제안한다. 제안된 기법은 인접한 기지국들과 릴레이들에게 서로 다른 주파수 자원을 할당하여 간섭을 줄임으로서 높은 데이터 전송영역의 확장이 가능하며, 기지국들과 릴레이들이 동시에 동작할 때 각 섹터에서 전체 주파수 대역을 사용함으로서 주파수 효율성을 높일 수 있다.