• Korean Journal of Veterinary Service
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• v.34 no.1
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• pp.1-4
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• 2011

A surface plasmon resonance imaging (SPRI) assay was developed for measuring porcine circovirus type 2 (PCV2) antibody using a recombinant capsid protein as an antigen. The diagnostic potential of SPRI for detecting antibodies to the PCV2 capsid protein was compared with that of a conventional enzyme-linked immunosorbent assay (ELISA) using 70 pig serum samples taken from 6 pig farms. There was a strong positive correlation between the SPRI and ELISA (n = 70, r = 0.911, P<0.01). Therefore, this recombinant capsid protein can be used as an antigen for serological studies, and the SPRI, a label-free and high-throughput method, is expected to be a valuable tool in the serodiagnosis of PCV2 infection.

• 한국생물공학회:학술대회논문집
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• 2005.04a
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• pp.473-473
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• 2005

• 한국생물공학회:학술대회논문집
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• 2005.04a
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• pp.467-467
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• 2005

• Proceedings of the Korean Society of Toxicology Conference
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• 2005.05a
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• pp.196-196
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• 2005

• Proceedings of the Korean Society for Applied Microbiology Conference
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• 2004.06a
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• pp.196-200
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• 2004

• Proceedings of the Korean Society of Life Science Conference
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• 2007.10a
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• pp.118.1-118.1
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• 2007

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• Proceedings of the KIEE Conference
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• 2003.07c
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• pp.1944-1946
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• 2003

질병의 발현과 직접적인 관련이 있는 단백질의 검출, 정량화하는 분석 장비를 소형화 할 수 있는 방법을 소개하고 그 가능성을 실험적으로 확인하였다. 단백질 검출을 위한 형광측정방법에서 가장 큰 문제인 여기광과의 혼재로 인한 신호 대 잡음 비를 해결하기 위해 마이크로 프리즘을 이용한 여기 방식을 고안하고 설계, 시뮬레이션 하였으며, 선행 실험을 통해 프리즘의 이용한 형광검출방법이 신호 대 잡음 비의 향상과 분석 시스템의 소형화에 효과적임을 확인하였다.

• Proceedings of the PSK Conference
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• 2002.04a
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• pp.156.1-156.1
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• 2002

• Journal of Life Science
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• v.17 no.2 s.82
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• pp.235-240
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• 2007

AvrRpt2 protein triggers hypersensitive response (HR) and strong disease resistance when it is translocated from a bacterial pathogen Pseudomonas sp. to host plant cells containing a cognate RPS2 resistance protein through Type III Secretion System (TTSS). However, AvrRpt2 protein can function as the effector that suppresses a basal defense and enhances the disease symptom when functional RPS2 resistance protein is absent in the infected plant cells. Using Affymetrix Arabidopsis DNA chip, we found that many genes were specifically regulated by AvrRpt2 protein in the rps2 Arabidopsis mutant. Here, we showed that expression of AtERF11 that is known as a member of B1a subcluster of AP2/ERF transcription factor family was down regulated specifically by AvrRpt2. To determine its function in plant resistance, we also generated the Arabidopsis thaliana transgenic plants constitutively overexpressing AtERF11 under CaMV 355 promoter, which conferred an enhanced resistance against a bacterial pathogen, Pseudomonas syringae pv. tomato DC3000. Thus, these results collectively suggest that AtERF11 plays a role as a positive regulator for disease resistance against biotrophic bacterial pathogen in plant.

• BMB Reports
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• v.44 no.11
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• pp.705-712
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• 2011

Advances in the fields of proteomics and genomics have necessitated the development of high-throughput screening methods (HTS) for the systematic transformation of large amounts of biological/chemical data into an organized database of knowledge. Microfluidic systems are ideally suited for high-throughput biochemical experimentation since they offer high analytical throughput, consume minute quantities of expensive biological reagents, exhibit superior sensitivity and functionality compared to traditional micro-array techniques and can be integrated within complex experimental work flows. A range of basic biochemical and molecular biological operations have been transferred to chip-based microfluidic formats over the last decade, including gene sequencing, emulsion PCR, immunoassays, electrophoresis, cell-based assays, expression cloning and macromolecule blotting. In this review, we highlight some of the recent advances in the application of microfluidics to biochemistry and molecular biology.