톡소포자충의 lactate dehydrogenase를 이용한 단클론 항체의 생산

Alternative Title
Minh Anh Dang Trinh
Author(s)
Trinh, Min Anh Dang
Alternative Author(s)
Minh Anh Dang Trinh
Advisor
신호준
Department
일반대학원 의학과
Publisher
The Graduate School, Ajou University
Publication Year
2009-02
Language
eng
Keyword
Toxoplasma gondiilactate dehydrogenasecell fusion techniquemonoclonal antibodies
Alternative Abstract
Background/Purpose: Toxoplasma gondii is one of the most common parasitic infections of human and other warm blooded animals. Because of the geographical distribution of toxoplasmosis, there is a need to develop a sensitive, rapid, simple and an inexpensive test for the early screening of patiens. In this study, to create the dipstick kit that has high sensitivity against LDH (lactate dehydrogenase) of T. gondii, at the first of all, hybridoma cell lines producing monoclonal antibodies with high affinity and specificity against T. gondii LDH (TgLDH) were established. Methods: After 6-8 week old BALB/c mice were immunized with synthetic peptides of TgLDH, splenocytes were harvested. To get the monoclonal antibodies (McAbs), splenocytes were fused with myeloma cells using PEG by a cell fusion technique. Hybridoma cells were selected by ELISA and subcloned through a limiting dilution method. McAbs were characterized by isotyping. Results: Eight McAb-producing hybridoma cells were selected. After three times of limiting dilution, eight clones, 1A10, 1B12, 3B2, 3B6, 1C12, 3C8, 3G6 and 3H1, were selected. OD values of eight monoclonal antibodies were ranged from 0.938 to 1.269 by ELISA. All eight McAbs isotypes were IgM class. Conclusion: These results indicated that eight hybridoma clones had strong reactivity to TgLDH and may be useful for diagnosis to T. gondii infection.
URI
https://dspace.ajou.ac.kr/handle/2018.oak/17067
Fulltext

Appears in Collections:
Graduate School of Ajou University > Department of Medicine > 3. Theses(Master)
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse