• Title/Summary/Keyword: 형광성

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Effect of Incubation Time after Cooling on the Meiotic Spindle and Chromosomes of Mouse Oocytes (냉각 후 배양시간이 생쥐 난자의 방추체와 염색체에 미치는 영향)

  • Yu I.
    • Journal of Embryo Transfer
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    • v.19 no.3
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    • pp.283-289
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    • 2004
  • This study was conducted to determine the effects of incubation time after cooling on mouse meiotic spindle and chromosome alignment and the optimal incubation time for their restoration. Oocytes at the metaphase II were obtained from superovulated mice. Control oocytes were held at 37$^{\circ}C$ during the experiment. Oocytes were rapidly cooled to $0^{\circ}C$, held for 30 minutes, warmed and incubated at 37$^{\circ}C$ for 5, 15, 30, 60 and 120 minutes, respectively. The morphological features of spindle and chromosomes in oocytes were evaluated by immunofluorescent staining. Meiotic spindle of control oocytes exhibited a normal-looking bipolar configuration(barrel-shaped) and highly fluorescent microtubles. The chromosomes were clustered in a discrete bundles at metaphase plate. Disassembly of meiotic spindle and chromosome dispersion were occurred immediately after chilling of oocyte. Fluorescence intensity index(FIS), normal chromosomes aligned and normal spindle configuration were compared according to incubation time at 37$^{\circ}C$. Restoration of a barrel-shaped spindle and normal chromosome alignment was occurring after 5 minutes incubation at 37$^{\circ}C$, improved as a incubation time increased, and decreased gradually after 120 minutes incubation(P<0.05). The optimal incubation time for restoration of meiotic spindle and chromosomes in cooled oocytes was 60 minutes.

An Improved Laser-Induced Fluorimetry for Assay of Uranium in Urine (레이저 유발형광법을 이용한 우라늄 작업자의 뇨 형광 분석)

  • Lee, Sang-Mok;Shin, Jang-Soo;Kim, Cheol-Jung
    • Nuclear Engineering and Technology
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    • v.25 no.2
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    • pp.255-258
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    • 1993
  • A method for analysis of trace uranium in urine sample was studied using a time-resolved $N_2$-laser-induced fluorimetry. The Fluran solution was found to be efficient to mask the chloride ions which are known to quench uranium fluorescence in the fluorimetric assay of uranium in urine. This improved method made the sample preparation much simpler than other conventional ones. The fluorescence intensities at 1% urine mixture with 10% Fluran aqueous solution showed good linearities in the concentration range of 10-500 ppb(before dilution).

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Spectrofluorometric Characteristics of the N-Terminal Domain of Riboflavin Synthase (아미노-말단 리보플라빈 생성효소 단백질의 형광 특성)

  • Kim, Ryu-Ryun;Yi, Jeong-Hwan;Nam, Ki-Seok;Ko, Kyung-Won;Lee, Chan-Yong
    • Korean Journal of Microbiology
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    • v.47 no.1
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    • pp.14-21
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    • 2011
  • Riboflavin synthase catalyzes the formation of one molecule of each riboflavin and 5-amino-6-ribitylamino-2,4-pyrimidinedione by the transfer of a 4-carbon moiety between two molecules of the substrates, 6,7-dimetyl-8-ribityllumazine. The most remarkable feature is the sequence similarity between the N-terminal half (1-97) and the C-terminal half domain (99-213). To investigate the structure and fluorescent characteristics of the N-terminal half of riboflavin synthase (N-RS) in Escherichia coli, more than 10 mutant genes coding for the mutated N-terminal domain of riboflavin synthase were generated by polymerase chain reaction. The genes coding for the proteins were inserted into pQE vector designed for easy purification of protein by 6X-His tagging system, expressed, and the proteins were purified. Almost all mutated N-terminal domain of riboflavin synthases bind to 6,7-dimethyl-8-ribityllumazine and riboflavin as fluorescent ligands. However, N-RS C47D and N-RS ET66,67DQ mutant proteins show colorless, indicating that fluorescent ligands were dissociated during purification. In addition, most mutated proteins show low fluorescent intensity comparing to N-RS wild type, whereas N-RS C48S posses stronger fluorescent intensity than that of wild type protein. Based on this result, N-RS C48S can be used as the tool for high throughput screening system for searching for the compound with inhibitory effect for the riboflavin synthase.

형광 발광층과 인광 발광층으로 구성된 하이브리드 발광층을 가진 청색 유기발광소자의 색 순도와 색안정성 증진

  • Bang, Hyeon-Seong;Chu, Dong-Cheol;Kim, Tae-Hwan;Seo, Ji-Hyeon;Kim, Yeong-Gwan
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.02a
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    • pp.272-273
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    • 2011
  • 유기발광소자는 차세대 디스플레이 소자로서 빠른 응답 속도, 높은 색 재현성 및 매우 얇은 두께로 제작이 가능한 장점을 가지고 있어서 차세대 디스플레이 소자로서 많은 응용 가능성을 가지고 있다. 청색 유기발광소자는 적색 및 녹색의 유기발광소자의 발광 효율 특성보다 상대적으로 효율이 떨어지고, 색 순도가 낮으며 수명이 짧은 단점을 가지고 있어 소자 특성을 개선해야 한다. 본 논문에서는 청색 유기발광소자의 색 순도와 색 안정성 증진을 위하여 발광층을 2개의 층으로 나누어 15 nm 두께의 4,4'-Bis(2,2-diphenyl-ethen-1-yl)diphenyl (DPVBi) 형광 청색 호스트 물질에 4,4 '-Bis[4-(diphenylamino)stylyl]biphenyl (BDAVBi) 형광 청색 게스트 물질을 첨가하여 제 1 형광 발광층을 형성하고 15 nm 두께의 4,4'-Bis(carbazol-9-yl)biphenyl (CBP) 인광 호스트 물질에 bis(3,5-difluoro-2-(2-pyridyl)phenyl-(2-carboxypyridyl)iridium III (FIrpic) 인광 게스트 물질을 첨가한 제 2 인광 발광층으로 구성된 30 nm 두께의 하이브리드 발광층을 사용하여 청색 유기 발광소자를 제작하고 전기적 특성과 광학적 성질을 조사하였다. 하이브리드 발광층을 사용하여 제작된 유기발광소자는 20 mA/cm2의 전류 밀도에서 6.2 cd/A의 발광 효율을 나타내었고, 최대 밝기는 약 16,200 cd/m2로 측정 되었다. 하이브리드 발광층을 사용한 청색 유기발광소자는 전류의 흐름이 단일 발광층 유기발광소자에 비교하여 상대적으로 안정적인 전류 흐름을 가지며 발광층 내부에 더 많은 정공과 전자를 포획하여 엑시톤 형성 확률이 증가하여 발광효율과 밝기가 향상되었다. 하이브리드 발광층을 적용한 유기발광소자는 469 nm파장에서 형광 발광층의 주 전계발광 피크가 나타났고 그와 함께 인광 발광층의 부 전계발광 피크가 491 nm의 파장에서 관측되었다. 또한 전계발광 스펙트럼의 반치폭이 10 nm 감소하여 청색의 색 순도 증가에도 기여하였다. 하이브리드 발광층을 가진 청색 유기발광소자의 색 좌표는 전압 변화에 관계없이 일정한 값을 나타내었다. 이러한 결과는 형광과 인광 발광층으로 구성된 하이브리드 발광층 유기발광소자가 전기적으로 안정성을 가지며 발광 특성을 개선하고 안정적인 청색 유기 발광 디스플레이 소자로 사용 가능함을 나타내고 있다.

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Preparation of Eu-doped $YVO_4$ Red Phosphors by Solid-State Reaction Technique

  • Jang, Jae-Yeong;Bang, Jun-Hyeok;An, Se-Hyeok;Ma, Gwon-Do;Kim, Chun-Su;Jo, Sin-Ho
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.08a
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    • pp.330-331
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    • 2011
  • 희토류 이온이 첨가된 형광체는 조명, 정보 디스플레이, 태양 에너지 변환 소자에 응용 가능하기 때문에 상당한 주목을 받고 있다. 특히, 결정 입자의 형상과 크기는 산업체 응용에 있어서 중요한 변수 중의 하나이다. 구형의 형광체 입자는 형광층의 광학 및 기하학적 구조를 최적화 시킬 수 있고, 결정 입자의 크기는 양질의 코팅을 위해 필요한 결정 입자의 양에 영향을 미친다. 본 연구에서는, $YVO_4$ 모체 결정에 Eu 이온의 농도를 선택적으로 주입하여 발광 효율이 높은 적색 형광체를 합성하고자 한다. 형광체 분말 시료는 활성체인 Eu의 함량을 0.00, 0.05, 0.10, 0.15, 0.20 mol로 변화시키면서 고상 반응법을 사용하여 합성하였다. 볼밀링 작업을 수행한 후에, 60$^{\circ}C$에서 20시간 건조하였고, 잘게 갈아서 체로 걸러낸 다음에 세라믹 도가니에 넣고 전기로에서 서서히 온도를 승온시켜 500$^{\circ}C$에서 10시간 동안 하소를 실시한 후에 1,100$^{\circ}C$에서 5시간 동안 소결하였다. Eu 이온의 함량비를 변화시켜 합성한 $YVO_4$ : Eu 형광체 분말 시료의 발광 세기의 변화, 결정 구조와 표면 형상을 각각 PL과 PLE, XRD, FE-SEM 장치를 사용하여 측정한 결과들을 종합해 볼 때, Eu 이온의 비가 0.15 mol일때 발광 세기가 최대값을 나타냄을 알 수 있었으며, 더욱 Eu의 함량을 증가시키자 농도 억제 현상에 의하여 발광 세기는 급격히 감소함을 보였다. SEM으로 촬영한 결정 입자의 형상의 경우에, Eu 이온의 함량비가 증가함에 따라 결정 입자들이 더욱 조밀하게 구형에 가까운 형상을 나타냄을 관측할 수 있었다(Fig. 1). 형광체 분말의 형광 스펙트럼의 경우에, 619 nm에 주 피크를 갖는 적색 형광 스펙트럼들이 관측되었으며, Eu 이온의 함량비에 따라 형광 세기는 상당한 의존성을 나타내었다(Fig. 2). Eu 함량에 따른 결정입자의 크기, 형광 세기와 회절 피크의 반치폭 사이의 상관 관계를 제시하고자 한다.

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A Transient Model Analysis of a Fluorescent Lamp at Startup Time (형광램프의 기동시 과도특성 모델 해석)

  • 함중걸;백수현
    • The Proceedings of the Korean Institute of Illuminating and Electrical Installation Engineers
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    • v.10 no.5
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    • pp.52-56
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    • 1996
  • Fluorescent lamps are widely accepted to energy efficient commercial lighting applications. In designing a fluorescent lamp system, a ballast design heavily relies on the characteristic of a fluorescent lamp under consideration. Especially, at startup time, the transient characteristic of a fluorescent lamp puts much tighter specification of a design. In this paper, based on the transient characteristic at the startup time, a transient behavioral model of a fluorescent lamp is presented with an equivalent circuit. The model is applicable to the wide range of fluorescent lamps provided by different manufacturers. The experimental results are compared with the results provided by PSPICE simulation. The result shows the model is effective In practice. As a result, we could identify more accurate startup constraints to decide the design of either an electro mechanical or an electronic ballast.

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Studies on Membrane Fouling Monitoring by Fluorescence Nano Particle and Fluorescent Spectrometry (형광 나노 입자 및 형광 분광 분석을 이용한 막오염 측정법 연구)

  • Seo, Mi-Rae;Nam, Mi-Yeon;Kim, Beom-Sik;Nam, Seung-Eun;Kim, In-Chul;Park, You-In
    • Membrane Journal
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    • v.21 no.2
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    • pp.163-170
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    • 2011
  • Membrane fouling control in water treatment may be the main obstacle for wider implementation and lower cost. A novel fluorescent spectroscope sensor device for membrane fouling integrity monitoring has been developed and evaluated in this study. PSf membranes for water treatment has been fabricated with three types of organic fluorescent materials, OB, FP, KCB. The fluorescent signal from membrane surface was analyzed throughout the filtration process. It was found that the fluorescent signal due to the membrane fouling decreased and the developed device is reliable for membrane fouling monitoring.

Laboratory-scale fluorescence spectroscopic method using UV for monitoring soils contaminated with petroleum produce (자외선 형광 분석법을 이용한 유류 토양오염 모니터링 시스템의 현장 적용을 위한 기초 연구)

  • 김우진;박재우;이주인
    • Journal of Soil and Groundwater Environment
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    • v.7 no.4
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    • pp.48-58
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    • 2002
  • As a pilot experiment for developing the monitoring system for oil spill from storage tank, previous approach of monitoring contaminated oil from mixed soil sample had the limitation that it cannot reflect the real situations of the contamination. In this study, more realistic contamination condition and water contents were considered. Fluorescence intensity was not affected by water contents. To acquire the stability of media, sand, Ca-bentonite, alumina, Fe-oxide, bead and silica were tested. Only sand was suitable to our system. These results should provide basic information for constructing reliable monitoring system.

Determination of $Ca^{2+}$ by Fiber Optic Fluorosensor Based on the Conformational Change of the Protein Calmodulin (Calmodulin 단백질의 형태변화를 이용한 광섬유 형광센서에 의한 $Ca^{2+}$의 정량)

  • Ri, Chang-Seop;Yang, Seung Tae
    • Analytical Science and Technology
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    • v.8 no.3
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    • pp.221-227
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    • 1995
  • The fiber optic fluorosensor that shows a specific selectivity for calcium ion is studied. This sensor employs protein Calmodulin(CaM) which forms a fluorescent chelate with $Ca^{2+}$. A dialysis membrane is used to entrap a fluorescein isothiocyanate-labeled CaM solution at the common end of a bifurcated fiber optic bundle. The sensing mechanism of this sensor is based on the shifts in the fluorescence spectrum of metal-calmodulin complexes which FCaM forms a chelate with $Ca^{2+}$. Upon binding with $Ca^{2+}$, CaM undergoes a conformational change which induces a change in the fluorescence of FCaM. This change in fluorescence signal which is measured by photomultiflier tube is related to the concentration of $Ca^{2+}$ for calibration curve. Detection limit for $Ca^{2+}$ and the interference effects by $Mg^{2+}$, $Eu^{3+}$ and $La^{3+}$ for this sensor are studied. Response time and life time for this fluorosensor are also investigated.

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