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변상요,Byoung-Sam Yoo,Mi Ae Yoo,Young Keun Song 한국생물공학회 2007 Biotechnology and Bioprocess Engineering Vol.12 No.6
The ability of heartwood extract of Morus bombycis in controlling the melanogenesis in B16 melanoma was investigated. An inhibitory effect was observed when the dose concentration was less than 10 mg/L. When the dose was 10 mg/L, the extra-cellular melanin accumulated was only 5% of the control. Proteome analysis with 2-D PAGE and MALDI-TOF showed that there were various proteins involved in inhibitory melanogenesis. It seems that down-regulation of TRP2, vacuolar proton-translocating ATPase 100 kDa subunit isoform a1-I and V-ATPase E2 subunit were involved in melanosome development and regulation that could reduce melanin synthesis.
Effect of Foilum mori on Adipocyte Differentiation
변상요,Geun Won Lee 한국생물공학회 2003 Biotechnology and Bioprocess Engineering Vol.8 No.5
Several natural products were tested to control the differentiation of cultured human mesenchymal stem cell into adipocyte. The extent of the inhibitory effect on the conversion of adipose was measured using Oil red O staining, which stains accumulated lipid droplets in the cytoplasm of adipocyte. Of the various natural product extracts, the adipocyte differentiation was inhibited by an extract from Folium mori in the concentration range 1×10-4 ~5×10-2 g/mL. These results suggest that Folium mori has an inhibitory activity toward the adipose conversion, which is a major cause of obesity.
유중수 타입의 외관이 투명한 자외선 차단 화장료에 관한 연구
곽재훈,조용훈,변상요,김태훈 한국유화학회 2015 한국응용과학기술학회지 Vol.32 No.3
This study is related to the developing method of a transparent sunscreen cosmetic which has waterproofing property and no white turbidity when applied to skin. The transparent sunscreen is prepared by exploiting refractive index difference between oil-phase and water-phase of water-in-oil(W/O) emulsion. The sunscreen according to this study is prepared as a W/O type emulsion so that it is water-stable and water resistance. Also, the stability of W/O type emulsion is developed by adjusting the content of oil phase part and water phase part. As a result of this studying, the transparent W/O emulsion is prepared by adjusting the refractive index of oil-phase and water-phase within 0.004 and it is found that the stability of the transparent sunscreen is increasing when the water phase part is over 75% (w/w) of the W/O emulsion.Through clinical test of transparent sunscreen, the value of sun protection Factor(SPF) and Protection Factor of UVA(PFA) were determined. SPF and PFA values of transparent sunscreen were indicated 30.99±1.65 and 3.01±0.30.
이승진,변상요,Lee, Seung-Jin,Byun, Sang-Yo 한국생물공학회 1999 KSBB Journal Vol.14 No.6
본 연구에서는 인뇨에서 분리 정제한 urokinase와 유전자 재조합 CHO(Chinese Hamster Ovary) 세포 배양액으로부터 분리 정제한 pro-urokinase의 물리화학적 특성과 혈액 내에서의 효소활성을 비교 분석하였다. Two chain form인 urokinase와 single chain form인 pro-urokinase를 각각 순수 분리한 후, electrophoresis한 결과 모두 54 kd의 단일밴드를 나타냈다. 그러나 urokinase는 환원시켰을 때 33 kd과 21 kd으로 나누어짐을 확인하였으나 gel filtration결과 분자량이 54 kd 정도임을 확인되어 용액 내에서 단일분자로 존재함을 알 수 있었다. Urokinase와 pro-urokinase가 물리화학적으로 거의 동일한 구조를 가졌다는 사실은 isoelectro focusing에 의한 pI 값이 모두 8.6으로 동일하다는 점과, 아미노산 조성을 분석한 결과 동일하다는 사실로도 알 수 있었다. N-terminal 아미노산 서열을 분석한 결과, urokinase는 이중사슬구조이므로 N-terminal이 두개 존재하여 pro-urokinase의 서열(Ser-Asn-Glu-Leu-His-Gln-Val-Pro-Ser-Asn)이외에도, 159번째의 Ile다음부터 Ile-Gly-Gly-Glu-Phe-Thr-Thr-Ile-Glu가 같은 peak로 나타남을 확인하였다. 효소활성 조사결과 pro-urokinase와 urokinase는 모두 농도 의존적으로 혈전용해 활성을 보였으나, 특이하게도 짧은 반응시간동안에는 urokinase가 동일 농도 하에서 강한 활성을 보인 반면, 2시간이 지난 오랜 반응조건에서는 pro-urokinase가 혈전용해활성을 나타내었다. Fibrinogen에 대한 분해활성을 조사한 결과, urokinase는 혈장 내 fibrinogen을 상당히 손상시키지만, pro-urokinase는 거의 영향을 주지 않아 혈전선택성이 매우 좋음을 알 수 있었다. Characteristics and enzyme activity comparison was made between urokinase isolated from urine and pro-urokinase separated from CHO(Chinese Hamster Ovary) cell culture broth. Both of purified urokinase and pro-urokinase resulted 54Kd single band in electrophoresis. Urokinase which was proved as a single molecule by gel filtration showed two separated 33Kd and 21Kd bands by 2-mercaptoethanol reduction. Isoelectric forcusing resulted same pl value of 8.6 for both of them. N-terminal amino acid sequence of urokinase after 159th Ile was Ile-Gly-Gly-Glu-Phe-Thr-Thr-Ile-Glu which was different from another N-terminal sequence of Ser-Asn-Glu-Leu-His-Gln-Val-Pro-Ser-Asn. Thrombolytic activities of both of them were propotional to the enzyme concentration. Urokinase showed thrombolytic activities in an short period of reaction time. Pro-urokinase, however, showed high thrombolytic activity for 2 hours or longer period of reaction time.