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HVPE 방법에 의해 성장된 graded AlGaN 에피층의 특성
이찬빈,전헌수,이찬미,전인준,양민,이삼녕,안형수,김석환,유영문,Lee, Chanbin,Jeon, Hunsoo,Lee, Chanmi,Jeon, Injun,Yang, Min,Yi, Sam Nyung,Ahn, Hyung Soo,Kim, Suck-Whan,Yu, Young Moon,Sawaki, Nobuhiko 한국결정성장학회 2015 한국결정성장학회지 Vol.25 No.2
Compositionally graded AlGaN epilayer was grown by HVPE (hydride vapor phase epitaxy) on (0001) c-plane sapphire substrate. During the growth of graded AlGaN epilayer, the temperatures of source and the growth zone were set at $950^{\circ}C$ and $1145^{\circ}C$, respectively. The growth rate of graded AlGaN epilayer was about 100 nm/hour. The changing of Al contentes was investigated by field emission scanning electron microscope (FE-SEM) and energy dispersive spectroscopy (EDS). From the result of atomic force microscope (AFM), the average of roughness in 2 inch substrate of graded AlGaN epilayer was a few nanometers scale. X-ray diffraction (XRD) with the result that the AlGaN (002) peak ($Al_{0.74}Ga_{0.26}N$) and AlN (002) peak were appeared. It seems that the graded AlGaN epilayer was successfully grown by the HVPE method. From these results, we expect to use of the graded AlGaN epilayer grown by HVPE for the application of electron and optical devices. 본 논문에서는 Al 조성이 점진적으로 변화된 AlGaN 에피층을 HVPE (hydride vapor phase epitaxy) 방법에 의하여 성장하였다. 소스영역의 온도는 $950^{\circ}C$, 성장 영역의 온도는 $1145^{\circ}C$에서 연속적으로 (0001) 사파이어 기판위에 성장되었고, AlGaN 에피층은 시간당 100 nm의 성장률을 보였다. FE-SEM 측정과 EDS 측정으로부터 성장층의 Al 변화를 확인하였으며, AFM 측정결과 2인치 기판위에 성장된 graded AlGaN 에피층의 거칠기는 수십 nm였다. Al 조성의 변화는 XRD 측정에 의하여 확인하였으며, Al 조성 74 %의 (002) AlGaN의 주피크 관측과 함께 연속적으로 (002) AlN 층의 피크가 확인되었다. 이는 하나의 층에 사파이어 기판으로부터 Al 조성이 점진적으로 변화하는 에피층을 HVPE 방법으로 얻었음을 증명하며, 이 결과로부터 다양한 광소자 및 전자소자의 응용이 기대된다.
영남지방 한우 거세우의 경락 단가 및 경락 가격에 대한 도체형질별 기여도 분석
이찬빈,민경태,이승재,이호성,서자겸,김명후,김병우 한국동물유전육종학회 2023 한국동물유전육종학회지 Vol.7 No.3
In this study, Data were the carcass grade on each 53,829 head of hanwoo steers slaughtered 3 years before (2017, 2018, 2019), 32,910 head of hanwoo steers slaughtered after (2020, 2021, 2022) COVID-19 at Yeongnam region and 54,369 head of hanwoo steers slaughtered same period at except for Yeongnam region. To find out the contribution of carcass traits to auction price and total price were analyzed through regression coefficients by using multiple regression analysis. As environmental factors affecting these carcass traits, slaughter year and slaughter season were set and analyzed through the least square method. The results of slaughter year showed that the grade of carcass traits in Yeongnam region increased over the years. In addition, in the slaughter season, the grade of carcass traits in the fall was found to be excellent. According to the contribution analysis, the results of the contribution ratio to auction price of before and after COVID-19 in Yeongnam region and after COVID-19 in all regions except Yeongnam were the same in order of marbling score, backfat thickness, eye muscle area, carcass weight. Also, the contribution ratio to total price were the same in order of carcass weight, marbling score, backfat thickness, eye muscle area. The general carcass grade is intended to use and analyze data from Yeongnam region, which has excellent backfat thickness and carcass weight, also has the largest number of elite cows selected through the verification work of elite cow by Korea Animal Improvement Association, and use it as a means for strategies to increase farm’s income and advance to high quality about Korean beef.
폴리디메틸실록산 기반 마이크로패턴 채널 시스템을 이용한 단일 세포의 극성 신호에 관한 연구
서정수,이찬빈,판이자,왕잉샤이오,정영미,김태진 한국화학공학회 2020 Korean Chemical Engineering Research(HWAHAK KONGHA Vol.58 No.1
In this study, we produced the micropatterned channel system using polydimethylsiloxane (PDMS) and micromolding in capillaries (MIMIC) technology and evaluated cellular polarity signals through high-resolved imaging at the single-cell level. In cells treated with platelet-derived growth factor (PDGF), three types of key signals in cell migration; phosphoinositide 3-kinase (PI3 K), Rac, and Actin, were strongly activated in the front area compared to the rear region, whereas myosin light chain (MLC) showed no notable activity in the front and rear areas. Our results will, therefore, provide important information and methodology for studying the correlation between cell polarity signals and cell migration under the newly defined microenvironment. 본 연구에서는 폴리디메틸실록산(PDMS)과 모세관-미세몰딩(MIMIC) 기술을 활용하여 마이크로패턴 채널 시스템을제작하고, 단일 세포 수준에서 극성화 패턴으로 형성되는 분자 신호를 고해상도 세포 이미징을 통해 분석하였다. 이 과정에서 혈소판유래성장인자(PDGF)가 처리된 세포에서는 세포 이동에 중요한 세 종류의 신호인 포스포이노시티드 3- 인산화효소(PI3K), Rac 및 액틴(Actin) 신호가 선두(front)영역에서 후미(rear)영역에 비해 강하게 활성화 하는 데 반해, 마이오신 경쇄(MLC) 신호는 비특이적 경향성을 보여주었다. 본 연구 결과는 향후 마이크로패턴의 미세환경에서 세포극성화 신호와 세포 이동과의 상관 관계를 연구하는 데 중요한 도움이 될 것으로 사료된다.
이규영,이찬빈,김수인,이창우,Lee, Kyu-Young,Lee, Chan-Bin,Kim, Soo-In,Lee, Chang-Woo 한국진공학회 2010 Applied Science and Convergence Technology Vol.19 No.5
나노 소재의 물성을 측정하기 위하여 대부분의 연구 그룹에서는 크게 두 가지 분석 기법인 분광학을 이용한 분석과 나노트라이볼로지를 이용한 분석을 사용하고 있다. 분광학을 이용한 분석에는 NMR (Nuclear Magnetic Resonance), IR (Infrared Spectroscopy), Raman 등이 대표적이라 할 수 있고, 나노트라이볼로지를 이용한 분석에는 AFM (Atomic Force Micro-Scope), EFM (Electrostatic Force Microscope), KFM (Kelvin Force Microscope), Nanoindenter 등의 탐침을 이용한 측정 기법이 대표적이다. Nanoindenter는 물질의 탄성 및 경도를 측정 할 수 있으며 이를 통해 물질의 특성을 연구 하는 데에 사용된다. 그러나 이런 Nanoindenter의 압입 실험에서 압입 조건 등의 통제 변수가 다르면 그 결과 값도 바뀌는 것을 볼 수 있는데 본 실험에서는 이런 압입 조건 중 Load - Hold - Unload force의 속도 및 시간을 변화시켜 물질의 탄성계수와 경도가 어떠한 차이를 가지는지 연구하였다. Most research groups used two analysis methods (spectroscopy and nanotribology) to measure the mechanical properties of nano-materials: NMR (Nuclear Magnetic Resonance), IR (Infrared Spectroscopy), Raman Spectroscopy as the spectroscopy method and AFM (Atomic Force MicroScope), EFM (Electrostatic Force Microscope), KFM (Kelvin Force Microscope), Nanoindenter as the nanotribological one. Among these, the nano-indentation technique particularly has been recognized as a powerful method to measure the elastic modulus and the hardness. However, this technique are prone to considerable measurement errors with pressure conditions during measurement. In this paper, we measured the change of elastic modulus and hardness of an Al single crystal with the change of load, hold, and unload time, respectively. We found that elastic modulus and hardness significantly depend on load, hold, and unload time, etc. As the indent time was shortened, the elastic modulus value decreased while the hardness value increased. In addition, we found that elastic modulus value was more sensitive to indent load, hold, and unload time than the hardness value. We speculate that measurement errors of the elastic modulus and the hardness originate from the residual stress during indenting test. From our results, the elastic modulus was more susceptible to the residual stress than the hardness. Thus, we find that the residual stress should be controlled for the minimum measurement errors during the indenting test.
왕시형,이찬빈,김지은,현정은,임민소,차혁진,오세훈,최영현,정영미 생화학분자생물학회 2017 Experimental and molecular medicine Vol.49 No.-
Tumor necrosis factor-inducible gene 6 protein (TSG-6) has recently been shown to protect the liver from acute damage. However, the mechanism underlying the effect of TSG-6 on the liver remains unclear. Autophagy is a catabolic process that targets cell components to lysosomes for degradation, and its functions are reported to be dysregulated in liver diseases. Here we investigate whether TSG-6 promotes liver regeneration by inducing autophagic clearance in damaged livers. Mice fed a methionine choline-deficient diet supplemented with 0.1% ethionine (MCDE) for 2 weeks were injected with TSG-6 (the M+TSG-6 group) or saline (the M+V group) and fed with MCDE for 2 additional weeks. Histomorphological evidence of injury and increased levels of liver enzymes were evident in MCDE-treated mice, whereas these symptoms were ameliorated in the M+TSG-6 group. Livers from this group contained less active caspase-3 and more Ki67-positive hepatocytic cells than the M+V group. The autophagy markers ATG3, ATG7, LC3-II, LAMP2A and RAB7 were elevated in the M+TSG-6 group compared with those in the M+V group. Immunostaining for LC3 and RAB7 and electron microscopy analysis showed the accumulation of autophagy structures in the M+TSG-6 group. TSG-6 also blocked both tunicamycin- and palmitate-induced apoptosis of hepatocytes and increased their viability by inducing autophagy formation in these cells. An autophagy inhibitor suppressed TSG-6-mediated autophagy in the injured hepatocytes and livers of MCDE-treated mice. These results therefore demonstrate that TSG-6 protects hepatocytes from damage by enhancing autophagy influx and contributes to liver regeneration, suggesting that TSG-6 has therapeutic potential for the treatment of liver diseases.