• Journal of Ginseng Research
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• 제19권3호
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• pp.267-274
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• 1995

Vicilin and legumin, the storage Proteins of seed, were Purified from ginseng (Panax ginseng C.A. Meyer) endosperm cells. They were immunized in rabbits, and antibodies were raised respectively. Using these two antibodies, double immunogold labeling of vicilin and legumin was carried out to determine the gap of synthetic time and the transport pattern of vicilin and legumin in the ginseng endosperm cells. Vicilin and legumin were synthesized at the same time at early embryo developmental stage. They were secreted from the Golgi bodies and accumulated into the small vacuoles. As the endosperm cells developed, vicilin and legumin localized in the small vacuoles were gradually transported toward the large central vacuole where they were stored. Protein bodies were derived from the vacuoles filled with proteins and distributed in the endosperm cells of mature red seed. Protein bodies were various in size from 1 to 8 ${\mu}{\textrm}{m}$ in which vicilin and legumin were mixed each other. The number of small particles labeled on the vicilin was greater than that of large particles labeled on the legumin in the protein bodies indicating that the amount of vicilin is higher than that of legumin in the protein bodies.

• Applied Microscopy
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• 제32권3호
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• pp.247-255
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• 2002

두족류 Octopus minor와 Todarodes pacificus의 시엽내 신경전달물질을 분비하는 neuron의 특성 및 기능을 확인하기 위해 serotonin 및 somatostatin의 항체를 사용한 면역염색과 면역금표지법을 시행하였다. 면역염색 결과 항-somatostatin은 살오징어인 경우 항-serotonin 면역반응과 유사하게 나타났지만, 서해낙지에서는 외과립세포층의 큰 세포에서만 반응을 보였다. 항-serotonin을 이용한 면역금표지법은 살오징어인 경우 내과립세포층과 수질부의 신경세포에서는 세포질 $0.5{\mu}m^2$당 30개 정도의 금입자가 관찰되어 강한 반응을 보인 반면, 서해낙지에서는 17개 정도의 비교적 약한 반응을 보였다. 항-somatostatin에서는 살오징어의 외과립 및 내과립세포층 그리고 수질부의 반응된 세포의 세포질 $0.5{\mu}m^2$당 30개 정도의 금입자가 관찰되어 강한 반응을 보인 반면, 서해낙지의 외과립세포층의 세포에서는 3개 정도의 금입자만이 관찰되어 역시 약한 반응을 보였다. 이와 같이 시엽의 각 부위별 면역염색과 면역금표지법을 시행한 결과 2종류의 항체에 각각 양성반응을 보인 신경세포들이 두 종에서 다양하게 분포하고 있음을 확인했는데 특히 면역염색과 면역금표지법에 관한 반응외 정도를 비교하면 서해낙지에 비해 살오징어에서 비교적 강하게 나타났다.

• 한국전자현미경학회:학술대회논문집
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• 한국현미경학회 1997년도 제28차 춘계학술대회
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• pp.14-14
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• 1997

• Molecules and Cells
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• 제20권1호
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• pp.119-126
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• 2005

${\alpha}$-Expansins are bound to the cell wall of plants and can be solubilized with an extraction buffer containing 1 M NaCl. Localization of ${\alpha}$-expansins in the cell wall was confirmed by immunogold labeling and electron microscopy. The subcellular localization of vegetative ${\beta}$-expansins has not yet been studied. Using antibodies specific for OsEXPB3, a vegetative ${\beta}$-expansin of rice (Oryza sativa L.), we found that OsEXPB3 is tightly bound to the cell wall and, unlike ${\alpha}$-expansins, cannot be solubilized with extraction buffer containing 1 M NaCl. OsEXPB3 protein could only be extracted with buffer containing SDS. The subcellular localization of the OsEXPB3 protein was confirmed by immunogold labeling and electron microscopy. Gold particles were mainly distributed over the primary cell walls. Immunohistochemistry showed that OsEXPB3 is present in all regions of the coleoptile and root tissues tested.

• 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.

• 한국패류학회지
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• 제13권2호
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• pp.161-173
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• 1997

동양달팽이의 위 상피에서 섬유소 분해효소의 분비여부를 화확인하기 위해 세포화학적 방법과 immunogold labeoling mithod를 수행되었다. Nesiohelix samarangae의 위에선 3가지 종류의 원주상피가 관찰되었다. 이 중 TYpe1세포는 microvilli가 발달하고 매우 많은 분비과립을 함유하고 있었으며, Type2세포는 위로 치우친 핵과 전자밀도가 높은 세포질에 rER이 매우 발달해 있었다. Type3 세포는 섬모와 미세융모를 함께 가지고 있는 세포로서 분비과립을 약간 함유하는 것으로 관찰되었다. 세포화학적 방법으로 위 상피에서의 cellulase의 활성을 시험해본 결과 상피세포들의 대다수를 차지하는 Type 1세포들과 Type3 세포들의 분비과립들의 주변에서 cellulase활성이 높았고, immunogold staining결과는 황금입자가 위 상피의 분비과립 주위의 세포질과 rER의 막과 주변세포질, 그리고 상피세포들의 상단부 세포질 등에서 표지되었다. 이상의 모든 실험 결과는 동양달팽이의 위 상피세포에서 cellulase가 분비된다는 사실을 알았다.

• 한국어업기술학회:학술대회논문집
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• 한국어업기술학회 2000년도 춘계수산관련학회 공동학술대회발표요지집
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• pp.538-538
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• 2000

Histochemical, cytochemical, and immmunocytochemical investigations were conducted to find out the cellulase activities in the accessory glands of the digestive system in the oriental land snail Nesiohelix samarangae under the LM, SEM, and TEM. It was found that the Type 1 and Type 3 cells out of five types of the epithelial cells of the digestive gland were labeled with the immunogold(protein-A gold) particles. Otherwise, none of epithelial cells of the mucus gland and the salivary gland were not labeled with the immunogold particles.

• 한국동물학회지
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• 제34권1호
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• pp.31-43
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• 1991

In the present study, the localization of myosin and the pathway of myofibrilogenesis of skeletal muscle cells in culture were investigated by immunocytochemical methods including immunoelectron microscopy and hybridoma formation. There were manly free ribosomes in the cytosol of the myoblast. At 48 hr of the culture, the myofilaments started to form and at 72 hr began to assemble to form myoabrils. At this time the Z band appeared, but the sarcomeres did not link together. Aker 96 hr of culture, adjacent sarcomeres linked together and shotved the typical striation of the skeletal muscle fiber. Myosin was synthesized in free ribosomes at 24 hr of culture and localized at many myofilaments at 48 hr and assembled mvoabrils at 72 hr and at 120 hr of the culture, myosin was localized at thick filaments of the A band.

• Journal of Microbiology and Biotechnology
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• 제10권5호
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• pp.714-720
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• 2000

Antigens of Herpes simplex virus type 1 (HSV-1) strain F were immunoblotted to identify the most immunodominant one, and the localization of this antigen was then studied using immunoelectron microscopy. The 67.8 kDa antigen appeared to be the most immunodominant one in a mouse model, and it showed randomly scattered and partially clustered distribution on the surface of the virion. The localization study was performed using immunogold with polyclonal anti-HSV-1 sera produced from BALB/c mice, and immunofluorescence demonstrated that the viral products in the HSV-2 infected Vero cells were distributed throughout the infected host cell, however, mainly on the surface of the host membrane.

• 대한수의학회지
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• 제39권5호
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• pp.921-929
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• 1999

There have been a number of studies of gonadotropes secreting LH and FSH in the adenohypophysis, but the pattern of hormone storage and secretion of these cells still remains a controversial matter. In this study, we examined whether gonadotropes contained both of LH and FSH, and if so, how these hormones were distributed within the secretory granules. Hypophyseal sections of Korean native goat were simultaneously immunostained for LH and FSH antisera by protein A-gold technique. It was found that most gonadotropes contained both FSH and LH, but hormone storages in the secretory granules were some different among cells. Three types of gonadotropes were identified by the shape and size of the secretory granules and their hormone storage patterns. One type(I) of gonadotropes contained oval secretory granules, which immunoreactivity for FSH and LH were very weak. The size of secretory granules ranged from 160 to 310nm in diameter. Most granules contained both FSH and LH, but some contained only one of them. In another type(II) of gonadotropes, the immunreactivity and hormone storage patterns of the secretory granules were similar to those of type I cells. However, the secretory granules were round in shape and larger in size than those of type I. The other gonadotropes(type III) were distinctly distinguished by plenty of hormones in their secretory granules which were densely packed with numerous immunolabelled gold particles. These data are some inconsistent with other results that have been obtained in other ruminants like as cattle and sheep.