• Design & Manufacturing
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• v.2 no.2
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• pp.25-28
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• 2008

Micro fabrication of biochip such like lab-on-a-chip becomes increasingly important. In this study, we designed and manufactured of new molds which were main factors for forming process in order to mass produce of biochip using forming process. Forming analysis of biochip was performed by Moldflow software. Results of this study are able to design and manufacture the mold which can be easy to eject the workpiece by using the slide mechanism for biochip.

• KIPS Transactions on Computer and Communication Systems
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• v.9 no.5
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• pp.101-106
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• 2020

Since computer became available, much effort has been made to achieve information security. Even though memory protection defense mechanisms were studied the most among of them, the problems of existing memory protection defense mechanisms were found due to improved performance of computer and new defense mechanisms were needed due to the advent of the side-channel attacks. In this paper, we propose JMP+RAND that embedding random values of 5 to 8 bytes per page to defend against memory sharing based side-channel attacks and bridging the gap of existing memory protection defense mechanism. Unlike the defense mechanism of the existing side-channel attacks, JMP+RAND uses static binary rewriting and continuous jmp instruction and random values to defend against the side-channel attacks in advance. We numerically calculated the time it takes for a memory sharing-based side-channel attack to binary adopted JMP+RAND technique and verified that the attacks are impossible in a realistic time. Modern architectures have very low overhead for JMP+RAND because of the very fast and accurate branching of jmp instruction using branch prediction. Since random value can be embedded only in specific programs using JMP+RAND, it is expected to be highly efficient when used with memory deduplication technique, especially in a cloud computing environment.

• Journal of Korean Society for Quality Management
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• v.26 no.3
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• pp.130-140
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• 1998

Studies present a guide to parameter estimation of software reliability models using SAS JMP. In this paper, we consider only software reliability growth model(SRGM), where mean value function has a S-shaped growth curve, such as Yamada et al. model, and ohba inflection model. Besides these stochastic SRGM, deterministic SRGM's, by fitting Logistic and Gompertz growth curve, have been widely used to estimate the error content of software systems. Introductions or guide lines of JMP are concerned. Estimation of parameters of Yamada et al. model and Logistic model is accomplished by using JMP. The differences between Yamada et al. model and Logistic model is accomplished by using JMP. The differences between Yamada et al. model and Logistic model is discussed, along with the variability in the estimates or error sum of squares. This paper have shown that JMP can be an effective tool I these research.

• Design & Manufacturing
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• v.2 no.3
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• pp.28-31
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• 2008

In recent, the demand of high-productivity injection mold is increased because of the growth of international packaging market which is induced by an increase of population. The increase of productivity leads to the large-capacity injection molding machine and peripheral devices. For solving this problem, the stack mold which is based on the exsiting machine and device has researched in advanced countries actively. In this paper, as the preliminary research of stack mold development, the stack mold which has 2 level ${\times}4$ cavity was designed and fabricated. Besides, the motion and structural analysis were performed to verify the stability of developed stack mold.

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2006.05a
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• pp.575-576
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• 2006

Recently, the demand of high-productivity injection mold increases since the consumption of packaging grows in the world. Stack mold is composed of more than two molds and it has very high productivity and economic efficiency. In advanced country, stack mold which has $4Level{\times}96cavity$ was developed already but, in occasion of domestic mold industry, there is no study of stack mold. In this study, stack mold which has $2Level{\times}4cavity$ is developed for securing the technique of manufacturing high-productivity mold.

• Proceedings of the Korea Information Processing Society Conference
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• 2019.10a
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• pp.456-458
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• 2019

정보보안을 달성하기 위해서 컴퓨터가 보급된 이래로 많은 노력이 이루어졌다. 그중 메모리 보호 기법에 대한 연구가 가장 많이 이루어졌지만, 컴퓨터의 성능 향상으로 이전의 메모리 보호 기법들의 문제들이 발견되고, 부채널 공격의 등장으로 새로운 방어책이 필요 되었다. 본 논문에서는 프로그램에 정적 바이너리 재작성(Static Binary Rewriting) 기법을 통해 페이지(Page)마다 4~8byte 의 난수를 삽입하여 메모리 공유 기반 부채널 공격을 방어할 수 있는 2 가지 방법을 제시한다. 최근 아키텍처는 분기 예측(Branch Prediction)을 통해 jmp 명령어에 대한 분기처리가 매우 빠르고 정확하게 처리되기 때문에 난수를 삽입할 때 사용하는 jmp+rand 방식은 오버헤드가 매우 낮다. 또한 특정 프로그램에만 난수 삽입이 가능하므로 특히 클라우드 환경에서 중복제거 기능과 함께 사용하면 높은 효율성을 보일 수 있다고 예상한다.

• Proceedings of the Microbiological Society of Korea Conference
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• 2002.10a
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• pp.27-30
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• 2002

Ralstonia eutrupha JMP134 is a well-known soil bacterium which can metabolite diverse aromatic compounds and xenobiotics, such as phenol, 2,4-dichlorophenoxy acetic acid (2, 4-D), and trichloroethylene (TCE), etc. Phenol is degraded through chromosomally encoded phenol degradation pathway. Phenol is first metabolized into catechol by a multicomponent phenol hydroxylase, which is further metabolized to TCA cycle intermediates via a meta-cleavage pathway. The nucleotide sequences of the genes for the phenol hydroxylase have previously been determined, and found to composed of eight genes phlKLMNOPRX in an operon structure. The phlR, whose gene product is a NtrC-like transcriptional activator, was found to be located at the internal region of the structural genes, which is not the case in most bacteria where the regulatory genes lie near the structural genes. In addition to this regulatory gene, we found other regulatory genes, the phlA and phlR2, downstream of the phlX. These genes were found to be overlapped and hence likely to be co-transcribed. The protein similarity analysis has revealed that the PhlA belongs to the GntR family, which are known to be negative regulators, whereas the PhlR2 shares high homology with the NtrC-type family of transcriptional activators like the PhlR. Disruption of the phlA by insertional mutation has led to the constitutive expression of the activity of phenol hydroxylase in JMP134, indicating that PhlA is a negative regulator. Possible regulatory mechanisms of phenol metabolism in R. eutropha JMP134 has been discussed.

• Journal of the Korea Organic Resources Recycling Association
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• v.11 no.4
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• pp.49-56
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• 2003

The strain Ralstonia eutopha JMP134 (formerly Alcaligenes eutrophus JMP134) can degrade trichloroethylene(TCE) through a chromosomal phenol-dependent pathway. The phenol hydroxylase was previously found to be a single responsible enzyme for TEC degradation. Here, we demonstrate that a recombinant bacterium, R. eutopha AEK301, one of Tn5-induced mutants of JMP134 containing a recombinant plasmid pYK3011, degrades TCE in the absence of inducer, phenol and in the presence of various carbon sources. Complete removal of TCE ($50{\mu}M$) was observed in minimal medium containing only 0.05% ethanol as a carbon source within 24 hours. The bacterium removed $200{\mu}M$ of TCE to below detectable level within two days under non-selective pressure. When TCE concentration was increased up to $400{\mu}M$, the degradation had been continued until two days, then ceased with removal of 70% of detectable TCE.

• Korean Journal of Microbiology
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• v.38 no.4
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• pp.260-266
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• 2002

In this study, chromosomal DNA fragment related to the regulation of phenol metabolism in Ralstonia eutropha JMP 134 was cloned and sequenced. The result has shown that two open reading frames (ORF1 and ORF2) exist on this regulatory region. ORF1, which initiates from 454 bp downstream of the stop codon of the phenol hydroxylase genes, was found to be composed of 501 amino acids. ORF2, whose start codon is overlapped with the stop codon of ORFl, was found to contain 232 amino acids. The comparison of amino acid sequences with other proteins has revealed that ORF1 belongs to the family of NtrC transcriptional activator, whereas ORF2 shares high homology with the family of GntR protein, which is known to be a negative regulator. ORF1 and ORF2 were designated as a putative positive regulator, phlR2 and a negative regulator phlA, respectively. Possible regulatory mechanisms of phenol metabolism in this strain was discussed.

• Journal of Microbiology
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• v.34 no.4
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• pp.320-326
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• 1996

To analyze the effects of host versus plasmid on survival of 2, 4-degrading bacteria in environmental samples, strains Pseudomonas cepacia/pJP4, Alcaligenes JMP228/pJP4, P. cepacia/p712, and Alcaligenes JMP228/p712 were separately inoculated into samples of field soil, paddy soil, lake water, and river water, and then the changes of their populations were measured. The strains used contained a 2, 4-D degradative plasmid, either pJP4 conferring fast-growing property to the host or p712 conferring slow-growing property, and were resistant to antibiotics such that the inoculated strains could be enumerated against the indigenous microbial populations. In sterile environmental samples, these strains were stably maintained at the levels used for inoculation, except in sterile paddy soil where Alcaligenes JMP228 strains died drapidly. In natural soil samples for four strains declined steadily with time, but in naturla water samples their polulations fell rapidly at the early phase and then remained almost constant. When the environmentla samples were treated with 2, 4-D, P. cepacia/pJP4 and P. cepacia/p712 maintained significant numbers, while Alcaligenes JMP228/pJP4 and Alcaligenes JMP228/p712 declined significantly in most of the samples. The results indicated that the survivability of genetically modified microorganisms could vary depending on the environments and that their abundance in the environments under s2, 4-D selection was markedly influenced by the nature of the 2, 4-D degradative plasmid as well as type of the host strain.