• Journal of the Korea Institute of Information and Communication Engineering
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• v.15 no.4
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• pp.930-934
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• 2011

Variety of logics are used in communication system processor. SSTL2-II 2.5V logic was attempted to analyze data transmission characteristics by varying transmission line length and data speed. Stable characteristics were obtained in case when data speed was 400Mbps and transmission line length was 30cm

• Proceedings of the Korean Institute of Information and Commucation Sciences Conference
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• 2009.10a
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• pp.433-435
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• 2009

어떤 데이터를 전송할 경우 시스템의 설계에 좌우 되는 경우가 많다. 상호간에 정보를 전달 할 경우 오류 없이 정확히 전송하기 위한 여러 가지 요소 중에서 기본적인 베이스 설계 시 고려 사항, 전송속도, 프로세서의 Logic 선정에 관한 내용을 본 연구를 통해서 제안 하고자 한다. 본 연구는 FPGA의 구현 가능 Logic 중 SSTL2-II 2.5V Logic을 가지고 실험을 하였으며, 전송 선로의 길이 변화와 데이터 속도의 변화 시 얻어지는 데이터 특성을 살펴보았다. 제작된 PCB상에 30cm의 패턴과 케이블을 이용 하였고 전송속도변화에 따른 특성을 측정 하였다. 전송 선로의 길이가 30cm로 하고 데이터 속도가 100Mbps일 경우 비교적 안정한 특성을 얻었다.

• JSTS:Journal of Semiconductor Technology and Science
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• v.1 no.1
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• pp.50-69
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• 2001

Three kinds of high-speed signaling methods for synchronous DRAM (SDRAM) bus interface channels (PC-133, Direct-Rambus, and SSTL-2) were analyzed in terms of the timing budget and the physical transmission characteristics. To analyze the SDRAM bus interface channels, loss mechanisms and the effective characteristic impedance method were reviewed and the ABCD matrix method was proposed as an analytic and yet accurate method. SPICE simulations were done to get the AC responses and the eye patterns of the three SDRAM bus interface channels for performance comparisons. Recent progress and future trend for SDRAM bus interface standards were reviewed.

• Bulletin of the Korean Space Science Society
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• 1995.10a
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• pp.26-26
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• 1995

No Abstract, See Full Text

• Journal of Microbiology and Biotechnology
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• v.5 no.5
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• pp.305-308
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• 1995

From the plasmid library made from Sstl and San-digested genomic DNA of Streptomyces fradiae NRRL 2702, four positive clones were selected using an oligodeoxynucleotide probe from the N-terminal amino acid sequence of purified threonine dehydratase. The cloned gene for threonine dehydratase was a 2.0 kilo-base pair DNA fragment. The deduced amino acid sequence of PCR product (PCR245) was matched to that of the N-terminal part of threonine dehydratase from S. fradiae and this showed a high similarity to the threonine dehydratases of other organisms. This indicated that amino acid sequences of threonine dehydratases were highly conserved and the polypeptide product of the PCR245 was likely to be involved in the deamination of threonine.