• Proceedings of the Korean Information Science Society Conference
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• 1998.10a
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• pp.311-313
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• 1998

이동에이전트는 독립된 객체로서 자율성을 가지고 컴퓨터를 이동하며 부연된 임무를 수행하는 프로그램이다. 이동에이전트는 코드와 데이터로 구성된 프로그램이므로 쉽게 복제될 수 있다. 이렇게 복제된 이동에이전트를 이동에이전트 클론이라 한다. 복제된 클론은 원본과 구별이 불가능하다. 이것은 에이전트의 인증을 불가능하게 만들고 예상되지 않은 에이전트의 중복 수행을 야기하며 에이전트의 내부정보 유출 공격을 위한 수단으로 사용된다. 본 논문에서는 이동에이전트 클론에 의한 이러한 문제점을 고찰하고 온라인 상에서 클론의 존재를 탐지하고 실행을 방지하며 클론을 생성한 서버를 확인하는 프로토콜을 설계한다.

• Journal of Software Assessment and Valuation
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• v.8 no.2
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• pp.13-27
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• 2012

This paper presents a tree-pattern based code-clone detector as CCR(Code Clone Ransacker) that finds all clusterd dulpicate pattern by comparing all pair of subtrees in the programs. The pattern included in its entirely in another pattern is ignored since only the largest duplicate patterns are interesed. Evaluation of CCR is high precision and recall. The previous tree-pattern based code-clone detectors are known to have good precision and recall because of comparing program structure. CCR is still high precision and the maximum 5 times higher recall than Asta and about 1.9 times than CloneDigger. The tool also include the majority of Bellon's reference corpus.

• The Korean Journal of Zoology
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• v.31 no.4
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• pp.300-308
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• 1988

Human placental alkaline phosphatase (PLAP), one of the oncofetal antigen was purified from placentas through the procedures including butanol extraction, concanavalin A-Sephar-ose, DEAE-cellulose and Sephadex G-200 gel chromatography. Monoclonal antibodies (fibs) against human PMP were produced by hybridizing SP 210-Ag 14 mouse myeloma cells with spleen ceils of Balblc mice immunized with PLAP. Six stable monoclones uvere obtained by cloning tuvice in serial dilutions, and the monoclonal speclfidty of these MAbs was confirmed by biochemical and immunonogical criteria. Tumor marker의 하나인 태반형 alkaline phosphatase(PLAP)에 대한 단일 클론항체의 생산과 분석을 위하여, 태반조직을 재료로 butanol 추출법 및 concanavaline A-Sepharose, DEAE-cellulose, Sephadex G-200 gel 크로마토그라피법에 의하여 PLAP를 순수 분리하였다. 이를 항원으로 하여 하이브리도마 방법에 의해 항-PLAP 단일 클론항체를 생산 분비하는 안정된 6클론세포를 얻었으며 생화학적 및 면역학적 분석방법으로 이들의 단일 클론성을 확인하였다.

• Tuberculosis and Respiratory Diseases
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• v.47 no.2
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• pp.150-160
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• 1999

Background: The CREST syndrome is an indolent form of progressive systemic sclerosis. Although its clinical progress is indolent, pulmonary hypertension(PH) associated with CREST syndrome have grave prognosis with over 40 percent mortality rate at 2 year follow-up. But the pathogenesis of pulmonary hypertension in this disease is not known, and classified as either primary or secondary PH. Clonality of endothelial cell proliferation in plexiform lesion is a molecular marker which allows distinction between primary and secondary PH. We performed this study to know whether the PH associated with CREST syndrome is a variant of primary PH or is a secondary PH. Methods: We assessed the X-chromosome inactivation based on the methylation pattern of the human androgen-receptor gene by PCR(HUMARA). Endothelial cells in plexiform lesions from female patients(n=3) with PH associated with CREST syndrome were microdissected from paraffin blocks. Vascular smooth muscle cells and lung parenchyma were also microdissected for clonality studies. Results: The proliferating endothelial cells in 14 plexiform lesions were all polyclonal. Similarly proliferated smooth muscle cells from 5 vessels with medial hypertrophy were also polyclonal. Conclusion: These results suggest that the pulmonary hypertension associated with CREST syndrome has different pathogenesis from primary PH and to be classified as secondary PH.

• Korean Journal of Microbiology
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• v.37 no.2
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• pp.137-144
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• 2001

In order to investigate the diversity of bacterial community in the mud flat of Sunchon Bay, Chunnam province, diversity of amplified 16S rDNA was examined. Total DNA was extracted from sediment soils and 16S rDNAs were amplified using PCR primers based on the universally conserved sequences in bacteria. Clonal libraries were constructed and 111 clones were examined by amplified rDNA restriction analysis (ARDRA) using HaeIII. Clones were clustered based on restriction patterns using computer program, GelCompar II. One hundred different RFLP types were detected from 111 clones. The 20 clones were selected and sequenced according to dendrograms derived from ARDRA, to cover most of the bacterial diversity in the clone libraries. None of the clones were identical to any representatives in the Ribosomal Database Project small subunit RNA databases and GenBank. All sequences showed between 77 and 96.8% similarity to the known 16s rRNA sequence from cultured organisms. The 20 clones sequenced fell into seven major lineages of the domain Bacteria: alpha-, delta-, gamma-Proteobacteria, low G+C Gram positive bacteria, high G+C Gram positive bacteria, Sphingobacteria (Cytophaga) and Cyanobacteria (chloroplast). Among the clones, the Proteobacteria were dominant.

• Korean Journal of Agricultural Science
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• v.14 no.2
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• pp.401-408
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• 1987

Nine monoclonal antibodies directed against infectious bovine rhinotracheitis virus (IBRV) were prepared by using cell hybridization technique, and the biological properties of the antibodies were investigated by means of immunofluorescence, serum neutralization, and electrophoretic analysis. Eight of 9 monoclonal antibodies reacted specifically with the antigenic constituents of IBRV, infectious laryngotracheitis virus, Marek's disease virus, turkey herpesvirus, hog cholera virus, porcine parvovirus and transmissible gastroenteritis virus. However, the remaining one, 26-2 clone, was found to be cross-reactive with pseudorabies virus. Two monoclonal antibodies, 7-C-2 and 12-A-2, which had neutralizing activity, were reactive with the molecular weights of 72 kilo daltons (72K) and 125K of IBRV proteins electrophoretically separated, respectively. The monoclonal antibody, 3-H-3, which is corresponding to 94K of IBRV proteins, revealed no neutralizing activity. The cross-reactive monoclonal antibody, 26-2, was proved by electrophoretical analysis to be reactive with 100K of IBRV proteins and 40K of pseudorabies virus.

• Journal of Plant Biology
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• v.36 no.4
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• pp.415-423
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• 1993

대두의 uricase II cDNA를 탐침으로 plaque 혼성화 방법에 의해 해녀콩의 뿌리를 cDNA library로부터의 두 개의 phage 클론(λCINUO-01, λCINUO-02)을 선별하였다. 두 phage 클론은 약 1.6 kb와 1.0 kb의 insert를 갖고 있었으며 이들의 염기서열을 결정하기 위하여 pUC19과 pBSKS vector에 subcloing(pcCLNUO-01, pcCLNUO-02)하였다. Sanger법에 의해 염기서열을 결정한 결과, 두 클론은 각각 1,611 bp와 1,024 bp로 이루어져 있었으며 pcCINUO-01은 308개의 아미노산, pcCINUO-02는 301개의 아미노산을 암호화하는 open reading frame(ORF)을 갖고 있었다. 두 클론의 ORF의 염기서열은 대두의 uricase II와 각각 88.9%, 89.3%의 상동성을 보여주었으며, 아미노산 서열은 84.1%, 85.4%의 상동성을 보여주었다. pcCINUO-01의 경우, 종결코돈으로부터 313 NT 하류쪽에 진핵생물의 poly(A) 첨가신호인 AATAAA 서열이 존재하였으며 이로부터 21 NT 하류쪽에 17 잔기의 poly(A)가 존재하였다. 두 클론의 염기서열에서 추정된 아미노산 서열의 카르복시 말단에는 세포질에서 합성된 몇몇 단백질들이 peroxisome으로 수송되는데 필요한 신호서열인 Ser-Lys-Leu-COOH 서열이 존재하고 있었다. 두 클론의 염기서열을 토대로 아미노산 조성을 살펴본 결과, 염기성 아미노산(Arg, His, Lys)과 산성 아미노산(Asp, Glu)이 각각 46 대 35, 47 대 35의 비를 보여주었는데 이는 uricase II 단백질의 염기성 성질을 보여주는 결과로 추정된다. Northern 혼성화 결과 해녀콩에서 uricase II는 뿌리혹에서만 특이적으로 발현됨을 알 수 있었고 게놈 혼성화 반응 결과는 uricase II 유전자가 해녀콩 게놈상에 유전자 가족으로는 존재할 수 있음을 보여주었다.

• Korean Journal of Agricultural and Forest Meteorology
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• v.13 no.4
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• pp.171-175
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• 2011

This study was conducted to determine the susceptibility of 15 clones of native and foreign poplar species and their hybrids to Melampsora leaf rust and to select resistant clones at a nursery stool bed. Rust severities of individual trees were determined by estimating the percentage of infected leaves on the trees in addition to comparing the infected leaves with the infection diagrams. Three hybrids out of 15 clones were selected as resistant clones to the Melampsora leaf rust in Korea. Bong-wha 1 and Hyunsasi 3 belong to section Leuce, and Dorskamp belongs to section Aigeiros. Based on our results, we recommend Dorskamp as the best resistant clone to poplar leaf rust.

• Journal of Software Assessment and Valuation
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• v.7 no.1
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• pp.29-39
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• 2011

To evaluate the quality of clone detection tools, we should know how many clones the tool misses. Hence we need to have the standard code-clone reference corpus for a carefully chosen set of sample source codes. The reference corpus available so far has been built by manually collecting clones from the results of various existing tools. This paper presents a tree-pattern-based clone detection tool that can be used for automatic generation of reference corpus. Our tool is compared with CloneDR for precision and Bellon's reference corpus for recall. Our tool finds no false positives and 2 to 3 times more clones than CloneDR. Compared to Bellon's reference corpus, our tools shows the 93%-to-100% recall rate and detects far more clones.

• 프린팅코리아
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• v.8 no.9
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• pp.90-91
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• 2009

아이피에이 클론은 지난해 하반기부터 CRON의 CTP를 국내 시장에 본격적으로 공급하고 있다. 올해 상반기에만 16대를 공급했으며 연말까지 40대 판매를 자신하고 있는 아이피에이 클론의 UV CTP는 경제성과 생산성에서 높은 수준을 인정받고 있다. 또한 정밀도와 품질면에서도 고객들에게 호평을 받고 있다. 사용해본 고객들에게서 더욱 높은 평가를 받는다는 아이피에이 클론의 마케팅 전략과 제품군, 앞으로의 계획을 소개한다.