• Proceedings of the Korean Society of Sericultural Science Conference
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• 2003.10a
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• pp.91-92
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• 2003

For studies of unfolded protein response (UPR), we isolated differentially expressed genes in Bm5 cell line induced with treatment of tunicamycin, the synthesis inhibitor of N-linked oligosaccharides in cells and constructed the subtractive cDNA library enriching UPR-related genes. (omitted)

• Journal of Korea Technical Association of The Pulp and Paper Industry
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• v.41 no.5
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• pp.38-43
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• 2009

A conservation corrugated box for storing document archives was developed. The specifications of the double-walled E-flute corrugated conservation box were modified from those of the Library of Congress, USA. The Photographic activity test (PAT) of ISO 18916 was used to ensure protection of the archival contents from adverse effects of the container itself. Accelerated aging was conducted to evaluate the conservative properties of the box components. Atomic force microscopy was also used to evaluate changes in the cellulose surface due to accelerated aging.

• YAKHAK HOEJI
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• v.38 no.4
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• pp.366-371
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• 1994

To improve the identification power of TLC/HPTLC the in situ reflectance spectra obtained directly from plates with commercial scanner are used. The spectrum normalization should be carried out prior to comparing and searching the spectra from library for the identification of compounds. Because the reflectance does not obey the Lambert-Beer's law, there arise some problems in normalization. These problems could be solved to some extent by normalizing the spectra with regression methods. The spectra are manipulated with the regression function of a curve obtained from the correlation plot. When the parabola was used as the manipulating function, the spectra were identified with the accuracy of 97% and this result was better than that of conventionally used the point and area normalization method.

• Journal of Information Management
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• v.38 no.2
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• pp.59-83
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• 2007

This study develops and presents data modeling and metadata elements in order to build system based on FRBR for music resources. This process intends to build bibliographic system to systematically manage and efficiently retrieve music resources.

• Journal of Information Science Theory and Practice
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• v.1 no.1
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• pp.69-82
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• 2013

Although MAchine Readable Cataloging (MARC) and Functional Requirements for Bibliographic Records (FRBR) are currently the most broadly used bibliographic structures for generating bibliographic data in the library community, each has its own weaknesses in describing information resources in diverse media. If the MARC format could be implemented in a structure that reflects the multi-layered characteristics of FRBR, its use could address current problems and limitations in resource description. The purpose of this research is to propose an alternative approach that can integrate the heterogeneous bibliographic structures of MARC and FRBR through the applications of facet and facet analysis. The proposed faceted data model is expected to function as a conceptual structure that can mediate between MARC data elements and FRBR attributes in order to utilize these structures in a more reliable and comprehensive way.

• Proceedings of the SCSK Conference
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• 2003.09b
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• pp.480-507
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• 2003

A rapid and efficient method for analyzing the nonionic surfactants and silicone polymers, which control the shape and characteristics of cosmetic products and give influence on product quality, has been developed using Matrix-Assisted Laser Desorption Ionization Time of Flight Mass Spectrometry (MALDI- TOF IMS). The MALDI-TOF/MS could easily and effectively determine the molecular weight distribution and monomer units of nonionic surfactants. As a result, creating a library of mass spectrum data of surfactants used in cosmetic products using MALDI-TOF/MS and analyzing surfactants extracted from the products may become a useful method for detailed structural characterization of the surfactants. Furthermore, the MALDI-TOF/MS analysis was effective in obtaining the spectrum of silicone polymers from which the molecular weight distribution could be determined. The repetition units and structural data could also be obtained through molecular mass peaks. Additionally, the monomer ratio and terminal groups as properties of silicone copolymers could be determined

• The KIPS Transactions:PartA
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• v.8A no.4
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• pp.385-390
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• 2001

In this paper, we describe a blocking method of buffer overflow attack for secure operating system. Our team developed secure operating system using MAC and ACL access control added on Linux kernel. We describe secure operating system (SecuROS) and standardized Secure utility and library. A working prototype able to detect and block buffer overflow attack is available.

• Nuclear Engineering and Technology
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• v.38 no.7
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• pp.665-674
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• 2006

Three-dimensional neutron flux and fluence of Kori Unit 3 were evaluated using the synthesis technique described in Regulatory Guide 1.190 for all reactor geometry. For this purpose DORT neutron transport calculations from Cycle 1 to Cycle 15 were performed using BUGLE-96 cross-section library. The calculated flux and fluence were validated by comparing the calculated reaction rates to the measurement data from the dosimetry sensor set of the $5^{th}$ surveillance capsule withdrawn at the end of cycle 15 of Kori Unit 3. And then the best estimation of the neutron exposures for the reactor vessel beltline region was performed using the least square evaluation. These results can be used in the assessment of the state of embrittlement of Kori Unit 3 pressure vessel.

• Genomics & Informatics
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• v.16 no.2
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• pp.22-29
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• 2018

Incorporation of unique barcodes into fission yeast gene deletion collections has enabled the identification of gene functions by growth fitness analysis. For fine tuning, it is important to examine barcode sequences, because mutations arise during strain construction. Out of 8,708 barcodes (4,354 strains) covering 88.5% of all 4,919 open reading frames, 7,734 barcodes (88.8%) were validated as high-fidelity to be inserted at the correct positions by Sanger sequencing. Sequence examination of the 7,734 high-fidelity barcodes revealed that 1,039 barcodes (13.4%) deviated from the original design. In total, 1,284 mutations (mutation rate of 16.6%) exist within the 1,039 mutated barcodes, which is comparable to budding yeast (18%). When the type of mutation was considered, substitutions accounted for 845 mutations (10.9%), deletions accounted for 319 mutations (4.1%), and insertions accounted for 121 mutations (1.6%). Peculiarly, the frequency of substitutions (67.6%) was unexpectedly higher than in budding yeast (~28%) and well above the predicted error of Sanger sequencing (~2%), which might have arisen during the solid-phase oligonucleotide synthesis and PCR amplification of the barcodes during strain construction. When the mutation rate was analyzed by position within 20-mer barcodes using the 1,284 mutations from the 7,734 sequenced barcodes, there was no significant difference between up-tags and down-tags at a given position. The mutation frequency at a given position was similar at most positions, ranging from 0.4% (32/7,734) to 1.1% (82/7,734), except at position 1, which was highest (3.1%), as in budding yeast. Together, well-defined barcode sequences, combined with the next-generation sequencing platform, promise to make the fission yeast gene deletion library a powerful tool for understanding gene function.

• Biomedical Science Letters
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• v.2 no.2
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• pp.231-240
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• 1996

Human blood clotting (coagulation) factor 9 cDNA which codes for 461 amino acid has been cloned by screening human fetal liver cDNA library using PCR. This 1.4 kb cDNA spanning from the ATG initiation codon to the TAA termination codon was cloned into bacterial .expression vector pGEX-2T, generating pGEX-F9 plasmid. The plasmid pGEX-F9 expresses about 73 kDa GST (Glutathione S-transferase)-Factor 9 fusion protein when introduced into E. coli. Western blot analysis using polyclonal antibody raised against human factor 9 confirmed this fusion protein contains factor 9 protein. The level of GST-factor 9 expression was about 20% of total protein and the purification of fusion protein was efficiently achieved by using GST agarose bead based on one step purification protocol.