• 제목/요약/키워드: Surface labelling

검색결과 13건 처리시간 0.028초

K-ToBI (Korean ToBI) Labelling Conventions (Version 3.0)

  • Juo, Suo-Ah
    • 음성과학
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    • 제7권1호
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    • pp.143-169
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    • 2000
  • This chapter presents an overview of Korean intonational structure and proposes a revised version of K -ToBI (Korean TOnes and Break Indices), a prosodic transcription convention for Seoul Korean. In the new version of K-ToBI, a tone tier is separated into two tiers: a phonological tone tier and a phonetic tone tier. A phonological tone tier labels tones marking the prosodic structure of an utterance, and a phonetic tone tier labels individual tones of an AP and an IP conforming to the surface pitch contour. Labelling surface tonal patterns will provide us data to test the underlying tonal patterns and to build phonetic implementation rules.

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Immunocytochemical Study on the Translocation Mechanism of Glucose Transporters by Insulin

  • Hah, Jong-Sik;Kim, Ku-Ja
    • The Korean Journal of Physiology
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    • 제27권2호
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    • pp.123-138
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    • 1993
  • The mechanism of insulin action to increase glucose transport is attributed to glucose transporter translocation from intracellular storage pools to the plasma membrane in insulin-sensitive cells. The present study was designed to visualize the redistribution of the glucose transporter by means of an immunogold labelling method. Our data clearly show that glucose transporter molecules were visible by this method. According to the method this distribution of glucose transporters between cell surface and intracellular pool was different in adipocytes. The glucose transporter molecules were randomly distributed at the cell surface whereas the molecules at LDM were farmed as clusters. By insulin treatment the number of homogeneous random particles increased at the cell surface whereas the cluster forms decreased at the intracellular storage pools. It suggests that the active molecules needed to be evenly distributed far effective function and that the inactive molecules in storage pools gathered and termed clusters until being transferred to the plasma membrane.

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미세부유사의 수력학적 연구 활용을 위한 흡착성 방사성표지물로서의 99mTc 제조기법 연구 (Reserach of a Labelling Technique for Using 99mTc as an Adsorbable Radiotracer for Hydrodynamics Studies of Fine Sediments in Suspension)

  • 정성희;김종범;문진호;홍영돈
    • 방사선산업학회지
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    • 제4권1호
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    • pp.13-17
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    • 2010
  • The radioisotope labelling study was carried out for the sediment transport investigation. The fate of suspended solid materials is deeply related to the harbour siltation and the shoreline deformation that take place as a result of the artificial development of coastal area. In the experiment, $^{99m}TcO_4{^-}$ was chemically reduced and labelled in such a way that the labelled particles have the similar settling characteristics with the natural sediment. The radioisotope labelling techniques can be widely used for the natural resource exploration where the hydraulic dynamics of underground water and surface water are of importance.

Biotin 표지법에 의한 질트리코모나스의 표면 항원 분리 (Identification of surface antigens of Trichomonas vaginalis)

  • 우남식;민득영
    • Parasites, Hosts and Diseases
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    • 제31권1호
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    • pp.37-42
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    • 1993
  • 질트리코모나스(Trichomonasvqqin is)의 항원성 변이를 관찰하기 위해 원충의 표면 항원 (surface antigen)을 N-hydmwsuccinlmide-biotin(N반5-biotin)으로 표지 하고 표지된 표면 단백질과 토끼의 항혈청으로 면역침전(Immunoprecipitation; IP)시켰으며 sodium dodec낀 sulfate-polyacrylamide gel electrophoresis (SDS-PAGE)와 전기영동이적법을 시 행하였다. 살아있는 원충을 NHS-biotin으로 표지하여 표면 단백질을 분리하고 이를 질트리코모나스에 면역된 토끼 항혈청과 면역침전 시켰던 바 46, 60, 68, 90, 130 그리고 220 kDa에서 6개의 단백질이 항원성을 나타내었으며 질토리코모나스의 분리주인 HY-1, HV-15 및 ATCC 50148 주간에 차이는 없어 이들 6개 분획이 표면 항원성 발현에 중요한 역할을 할 것으로 생각된다.

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STUDIES ON THE I LABELLING OF CASTOR OIL, AND THE DETERGENCY OF SODIUM DODECYL SULFATE

  • 허용철;문병열;김영국
    • 대한화장품학회지
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    • 제10권1호
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    • pp.42-48
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    • 1984
  • The comparative detergency of Sodium dodecyl sulfate (SDS) solution near the first critical micelle concentration (CMC) was measured by means of a 131 I-labelled castor oil as a soil. More than 95% radiochemical purity of 131 I-labelled castor oil was obtained using potassium lidide as a carrier. Polyester test fabric was soiled with 131 I-labelled castor oil, and washed in a conventional washing apparatus mounted on appropriate devices. Fabric radioactivities were measured before and after washing by a scintilation counter. Near the first CMC, the detergency of SDS was increased with decreasing of surface tension of SDS. It was also shown that 131 I-labelled castor oil was useful for studying the detergency of SDS.

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전자현미경 기법을 이용한 Herpes simplex 2형 바이러스 항원의 면역학적 분석 (Immunoelectron Microscopic Localization and Analysis of Herpes simplex Virus Type 2 Antigens)

  • 김천식;오명환
    • 미생물학회지
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    • 제40권1호
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    • pp.23-28
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    • 2004
  • 단순포진 바이러스 감염을 유발하는Herpes simplex2형 바이러스의 감염에 관여하는 항원들과 중화항체 생산을 유발하는 주요 항원들의 위치를 확인하였다. Vero cell에 감염하였을 때 48시간 동안 31, 43, 59, 69 kDa 바이러스 항원들이 지속적으로 발현되었으며, 감염된 쥐에서 생산한 항체와의 반응에서는 51 kDa 항원이 가장 강한 반응을 보였다. 면역전자현미경으로 위치를 확인한 결과 colloidal gold가 바이러스 표면에 발견되는 것으로 보아 이 항원이 바이러스 표면에 존재하고 있는 것으로 확인되었다. 형광현미경 분석은 이 항원들이 감염된 세포 내에서 전반적으로 발견되었고 특히 세포 표면에서 많이 발현되고 있었다.

방사성오염물질 처분에 대한 고찰 (Consideration of Radioactive Contamination Materials Disposal)

  • 임현진;김태엽;이홍재;김진의;김현주
    • 핵의학기술
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    • 제14권2호
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    • pp.128-132
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    • 2010
  • 핵의학과 종합조작실은 방사선 관리구역으로 이곳에서 발생된 방사성오염물질은 방사성폐기물로 간주하여 일반쓰레기와 별도로 관리를 해야 한다. 본 실험은 우리가 미처 인식하지 못해 일반쓰레기로 처분되었던 방사성오염물질의 오염도를 측정하고 원인을 분석하여 보다 적극적인 방사성폐기물 관리 운영의 필요성을 제시하고자 함이다. 측정대상은 방사성의약품을 표지하기 위해 사용된 생리식염수와 $^{99}Mo$/$^{99m}Tc$ generator(국산 및 외산)에서 발생한 generator cap, saline needle cap, $^{99m}Tc$-needle cap, saline vial로 하였고, gamma survey meter를 이용하여 평균값과 표준 편차(mean${\pm}$SD)로 나타냈다. 측정대상물질의 오염유무를 알기 위해 방사선 관리구역에서 반출될 수 있는 물질의 표면오염도인 최대허용표면오염도의 1/10(43.2 cpm)을 기준값으로 정하였다. 각각의 표면오염도를 측정한 결과 방사성의약품 표지를 위해 사용된 생리식염수에서는 $14,429{\pm}26,378$ cpm으로 최대 허용표면오염도의 1/10을 초과하였다. 그리고 측정된 generator중 외산에서는 generator cap: $17{\pm}28$ cpm, saline needle cap: $35{\pm}66$ cpm, $^{99m}Tc$-needle cap: $9{\pm}21$ cpm, saline vial: $13{\pm}28$ cpm으로 최대허용표면오염도의 1/10를 초과하지 않았지만 국산에서는 generator cap: $22,852{\pm}52,545$ cpm, saline needle cap: $87,367{\pm}109,711$ cpm, $^{99m}Tc$-needle cap: $9,008{\pm}10,459$ cpm, saline vial: $186,416{\pm}158,196$ cpm으로 최대 허용표면오염도의 1/10를 초과하였다. 외산 generator에서 발생한 측정대상물질은 일반폐기물로 처분하고 국산 generator와 방사성의약품을 표지하기 위해 사용된 생리식염수는 반드시 방사성폐기물로 간주하여 처분해야 한다. 따라서 일반쓰레기 뿐만 아니라 종합조작실에서 반출되는 모든 물질에 대한 자체적인 방사선측정, 기록 및 비치와 방사성폐기물에 대한 지속적인 교육을 통해 방사성 폐기물이 일반쓰레기로 처분되어 나가는 것을 예방 할 수 있을 것이다.

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인슐린의 포도당 이동 촉진 기전에 관한 연구 -세포내부 미세구조와 Cytochalasin B 결합단백질의 분포- (A Study on the Mechanism of Insulin Sensitivity to Glucose Transport System: Distribution of Subcellular Fractions and Cytochalasin B Binding Proteins)

  • 하종식
    • The Korean Journal of Physiology
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    • 제24권2호
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    • pp.331-344
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    • 1990
  • What makes glucose transport function sensitive to insulin in one cell type such as adipocyte, and insensitive in another such as liver cells is unresolved question at this time. Recently it is known that insulin stimulates glucose transport in adipocytes largely by redistributing transporter from the storage pool that is included in a low density microsomal fraction to plasma membrane. Therefore, insulin sensitivity may depend upon the relative distribution of gluscose transporters between the plasma membrane and in an intracellular storage compartment. In hepatocytes, the subcellular distribution of glucose transporter is less well documented. It is thus possible that the apparent insensitivity of the hepatocyte system could be either due to lack of the constitutively maintained, intracellular storage pool of glucose transporter or lack of insulin-mediated transporter translocation mechanism in this cell. In this study, I examined if any intracellular glucose transporter pool exists in hepatocytes and this pool is affected by insulin. The results obtained summarized as followings: 1) Distribution of subcellular fractions of hepatocyte showed that there are $24.9{\pm}1.3%$ of plasma membrane, $36.9{\pm}1.7%$ of nucleus-mitochondria enriched fraction, $23.5{\pm}1.2%$ of lysosomal fraction, $9.6{\pm}1.0%$ of high density microsomal fraction and $4.9{\pm}0.5%$ of low density microsomal fraction. 2) In adipocyte, there were $29.9{\pm}2.6%$ of plasma membrane, $19.4{\pm}1.9%$ of nucleus-mitochondria enriched fraction, $26.7{\pm}1.8%$ of high density microsomal fraction and $23.9{\pm}2.1%$ of low density microsomal fraction. 3) Surface labelling of sodium borohydride revealed that plasma membrane contaminated to lysosomal fraction by $26.8{\pm}2.8%$, high density microsomal fraction by $8.3{\pm}1.3%$ and low density microsomal fraction by $1.7{\pm}0.4%$ respectively. 4) Cytochalasin B bound to all of subcellular fractions with a Kd of $1.0{\times}10^{-6}M$. 5) Photolabelling of cytochalasin B to subcellular fractions occurred on 45 K dalton protein band, a putative glucose transporter and D-glucose inhibited the photolabelling. 6) Insulin didn't affect on the distribution of subcellular fractions and translocation of intracellular glucose transporters of hepatocytes. 7) HEGT reconstituted into hepatocytes was largely associated with plasma membrane and very little was found in low density microsomal fraction which equals to the native glucose transporter distribution. Insulin didn't affect on the distribution of exogeneous glucose transporter in hepatocytes. From the above results it is concluded that insulin insensitivity of hepatocyte may due to lack of intracellular storage pool of glucose transporter and thus intracellular storage pool of glucose transporter is an essential feature of the insulin action.

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Toxoplasma gondii: Ultrastructural localization of specific antigens and inhibition of intracellular multiplication by monoclonal antibodies

  • Lee, Boo-Young;Ahn, Myoung-Hee;Kim, Hyun-Chul;Min, Duk-Young
    • Parasites, Hosts and Diseases
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    • 제39권1호
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    • pp.67-76
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    • 2001
  • This experiment was focused on the characterization of anti- Toxoplasma monoclonal antibodies (mAbs) and the effect of mAbs on the parasite invasion of mouse peritoneal macrophages. Twenty eight mAbs including M110, M556, R7A6 and M62l were characterized by Ab titer, immunoglobulin isotyping and western blot pattern. Antibody titer (optical density) of 4 mAbs. Ml 10. M556. R7A6 and M62l. were 0.53,0.67, 0.45 and 0.39 (normal mouse serum; 0.19) with the same IgGl isotypes shown by Enzyme-linked immunosorbent assay (ELISA). Western blot analysis showed that Ml 10. M556. R7A6 and M62l reacted with the 33 kDa (p30),31 kDa (p28),43 kDa and 36 kDa protein. Immuno-gold labelling of mAbs M110, M556, R7A6 and M621 reacted with the surface membrane, dense granules and parasitophorous vacuolar membrane (PVM) , rhoptries and cytoplasm of tachyzoite, respectively. For in vitro assay, preincubation of tachyzoties with four mAbs, Ml 10, M556, R7A6 and M62l resulted in the decrease of the number of infected macrophages (p < 0.05) and the suppression of parasite multiplication at 18 h post-infection. Four monoclonal antibodies including Ml 10 (SAGI) were found to have an important role in the inhibition of macrophage invasion and T. gondii multiplication in vitro, and these mAbs may be suitable for vaccine candidates, diagnostic kit and for chemotherapy.

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Spirometra erinacei에서 IgE와 IgG 항체를 유도하는 항원성분의 면역조직화학적 위치와 특성 (Immunohistochemical Localization and the Characteristics of Antigenic Compnent Inducing IgE and IgG Antibodies in Spirometra erinacei)

  • Chang-Hwan Kim;Sook-Jae Seo;Hong-Ja Kim;Kee-Hoon Kwak
    • 대한의생명과학회지
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    • 제2권1호
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    • pp.1-12
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    • 1996
  • Spirometra erinacei의 유충인 sparganum(metacercoid)에 감염되었을 때 호산성백혈구의 증가와 IgE 항체역가가 증가된다는 보고가 있다. 이 기생충에 감염되었을 때 IgG 항체와 IgE 항체를 유도하는 충체의 항원성분의 소재를 면역세포조직화학적 방법으로 충체의 성체와 유충에서 비교하였고, 또한 충체의 추출물을 SDS-PSGE와 EITB를 이용하여 IgG와 IgE 항체 유도 항원성분의 면역적 특성도 추구하였다. IgG와 IgE 항체 유도성분은 성체와 유충의 근층에서 공통적으로 분포되어 있었고, IgG 항원성분은 근층 뿐만 아니라 외피층과 유조직층에서도 반응이 나타났으며, 성체의 수태편절에서는 자궁 내에 있는 충난의 표면에서도 반응이 나타났다. 충체의 외피층에서 항원성분을 면역황금 표지법으로 관찰한 결과, 충체의 외피층(tegument)에서 IgG 항원성분의 분포밀도가 IgE 항원성분의 밀도보다 컸다. 충체의 추출물 중 IgG, IgE 유도 항원성 단백질의 면역학적 특성을 비교하였다. 성체의 추출물의 43개 분회 중 21개 분획이 IgG 항원성분으로서 반응하였고, IgE 항원성분으로는 21개 분획에서 반응하였다. 이들 중 11개 분획 (410, 304, 268, 174, 162, 116, 92, 86, 72, 60, and 59 kDa)에서 IgG와 IgE가 교차반응하였으며, 유충의 추출물의 36개 분획 중 IgG 항원성분으로 22개의 분획에서 반응이 나타났고, IgE 항원성분으로는 13개의 분획에서 반응하였으며, 이들 중 5개 분획(204, 116, 92, 79, and 59 kDa)에서 IgG와 IgE가 서로 교차반응하였다.

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