Detection of Serum Immunoglobulins in Wild Birds by Direct ELISA: A Methodological Study to Validate the Technique in Different Species Using Antichicken Antibodies
1. This study presents an easy protocol to measure the amount of immunoglobulins from the blood serum of different bird species in the wild (Ficedula hypoleuca Pallas, Parus caeruleus L., Lanius meridionalis Temminkck, Lanius collurio L., Athene noctua Scopoli and Falco tinnunculus L.) by direct enz...
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Veröffentlicht in: | Functional ecology 2003-10, Vol.17 (5), p.700-706 |
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creator | Martínez, J. Tomás, G. Merino, S. Arriero, E. Moreno, J. |
description | 1. This study presents an easy protocol to measure the amount of immunoglobulins from the blood serum of different bird species in the wild (Ficedula hypoleuca Pallas, Parus caeruleus L., Lanius meridionalis Temminkck, Lanius collurio L., Athene noctua Scopoli and Falco tinnunculus L.) by direct enzyme-linked immunosorbent assay, ELISA using commercial antichicken antibodies. 2. Additionally, the ELISA technique is validated for detecting serum immunoglobulins by means of other electrophoretic (sodium dodecyl sulphate polyacrylamide gel electrophoresis, SDS-PAGE, and native electrophoresis) and immunological (Western blot) methods. 3. The results by Western blot show that the commercial antibody recognized proteins with apparent molecular weight according to heavy and light chains of immunoglobulins. 4. Both ELISA and Western blot data were correlated, implying that the commercial antibody bound to immunoglobulins and not to other proteins or ELISA plates. Densitometric data achieved by SDS-PAGE and native electrophoresis were only correlated in some species indicating a problem in detecting clearly the heavy and light chains, and γ-globulin fraction, respectively. 5. It is concluded that the proposed protocol is easy to carry out and may be used to detect total serum immunoglobulins from most bird species. |
doi_str_mv | 10.1046/j.1365-2435.2003.00771.x |
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This study presents an easy protocol to measure the amount of immunoglobulins from the blood serum of different bird species in the wild (Ficedula hypoleuca Pallas, Parus caeruleus L., Lanius meridionalis Temminkck, Lanius collurio L., Athene noctua Scopoli and Falco tinnunculus L.) by direct enzyme-linked immunosorbent assay, ELISA using commercial antichicken antibodies. 2. Additionally, the ELISA technique is validated for detecting serum immunoglobulins by means of other electrophoretic (sodium dodecyl sulphate polyacrylamide gel electrophoresis, SDS-PAGE, and native electrophoresis) and immunological (Western blot) methods. 3. The results by Western blot show that the commercial antibody recognized proteins with apparent molecular weight according to heavy and light chains of immunoglobulins. 4. Both ELISA and Western blot data were correlated, implying that the commercial antibody bound to immunoglobulins and not to other proteins or ELISA plates. Densitometric data achieved by SDS-PAGE and native electrophoresis were only correlated in some species indicating a problem in detecting clearly the heavy and light chains, and γ-globulin fraction, respectively. 5. It is concluded that the proposed protocol is easy to carry out and may be used to detect total serum immunoglobulins from most bird species.</description><identifier>ISSN: 0269-8463</identifier><identifier>EISSN: 1365-2435</identifier><identifier>DOI: 10.1046/j.1365-2435.2003.00771.x</identifier><language>eng</language><publisher>Oxford, UK: British Ecological Society</publisher><subject>Animal, plant and microbial ecology ; Antibodies ; Biological and medical sciences ; Ecological genetics ; Ecological immunology ; Ecology ; Electrophoresis ; Enzyme linked immunosorbent assay ; Fundamental and applied biological sciences. Psychology ; Gels ; General aspects. 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This study presents an easy protocol to measure the amount of immunoglobulins from the blood serum of different bird species in the wild (Ficedula hypoleuca Pallas, Parus caeruleus L., Lanius meridionalis Temminkck, Lanius collurio L., Athene noctua Scopoli and Falco tinnunculus L.) by direct enzyme-linked immunosorbent assay, ELISA using commercial antichicken antibodies. 2. Additionally, the ELISA technique is validated for detecting serum immunoglobulins by means of other electrophoretic (sodium dodecyl sulphate polyacrylamide gel electrophoresis, SDS-PAGE, and native electrophoresis) and immunological (Western blot) methods. 3. The results by Western blot show that the commercial antibody recognized proteins with apparent molecular weight according to heavy and light chains of immunoglobulins. 4. Both ELISA and Western blot data were correlated, implying that the commercial antibody bound to immunoglobulins and not to other proteins or ELISA plates. Densitometric data achieved by SDS-PAGE and native electrophoresis were only correlated in some species indicating a problem in detecting clearly the heavy and light chains, and γ-globulin fraction, respectively. 5. It is concluded that the proposed protocol is easy to carry out and may be used to detect total serum immunoglobulins from most bird species.</description><subject>Animal, plant and microbial ecology</subject><subject>Antibodies</subject><subject>Biological and medical sciences</subject><subject>Ecological genetics</subject><subject>Ecological immunology</subject><subject>Ecology</subject><subject>Electrophoresis</subject><subject>Enzyme linked immunosorbent assay</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gels</subject><subject>General aspects. Techniques</subject><subject>Human ecology</subject><subject>humoral immunity</subject><subject>Immunoglobulins</subject><subject>Methods and techniques (sampling, tagging, trapping, modelling...)</subject><subject>Molecular weight</subject><subject>Western blot</subject><subject>Wild birds</subject><issn>0269-8463</issn><issn>1365-2435</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNkc2O0zAUhSMEEmXgDVjcDewa_Jc_xKa0HahUxKIzsLQS56Z1ceyO7Yjp-_CgJNPRsGXlK93zHV-dkyRASUqJyD8cU8rzbM4Ez1JGCE8JKQqa3j9LZk-L58mMsLyalyLnL5NXIRwJIVXG2Cz5s8KIKmpnwXWwQz_0sOn7wbq9cc1gtA2gLfzUpoXP2rcBmjOstB8ZWG83u8VHWMA3jAfXOuP2WtUGdnFozxAd_KiNbuuIEA8IN6gOVt8NOPmtdNehRxthd0KlMcBt0HYPCxu1Omj1C-3D3Lh2XL5OXnS1Cfjm8b1Kbq_XN8uv8-33L5vlYjtXQjA678qyYbwpClEo1mSiQcE6JkhTcEEFYlUoUmasozkiyVlJOIoaG9aotlRZK_hV8v7ie_JuPDRE2eug0JjaohuCpGVZZIxXo7C8CJV3IXjs5MnrvvZnSYmcapFHOaUvp_TlVIt8qEXej-i7xz_qMIbV-doqHf7xGS1YRemo-3TR_dYGz__tL6_Xy3EY8bcX_Bii8084z6qK5jn_C0k3qy4</recordid><startdate>200310</startdate><enddate>200310</enddate><creator>Martínez, J.</creator><creator>Tomás, G.</creator><creator>Merino, S.</creator><creator>Arriero, E.</creator><creator>Moreno, J.</creator><general>British Ecological Society</general><general>Blackwell Science Ltd</general><general>Blackwell Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SN</scope><scope>C1K</scope></search><sort><creationdate>200310</creationdate><title>Detection of Serum Immunoglobulins in Wild Birds by Direct ELISA: A Methodological Study to Validate the Technique in Different Species Using Antichicken Antibodies</title><author>Martínez, J. ; Tomás, G. ; Merino, S. ; Arriero, E. ; Moreno, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4421-f88b23b7747c2b54be42f240b73414ee97c0852f16ee062803e4aeb2bcd8c5d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animal, plant and microbial ecology</topic><topic>Antibodies</topic><topic>Biological and medical sciences</topic><topic>Ecological genetics</topic><topic>Ecological immunology</topic><topic>Ecology</topic><topic>Electrophoresis</topic><topic>Enzyme linked immunosorbent assay</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gels</topic><topic>General aspects. Techniques</topic><topic>Human ecology</topic><topic>humoral immunity</topic><topic>Immunoglobulins</topic><topic>Methods and techniques (sampling, tagging, trapping, modelling...)</topic><topic>Molecular weight</topic><topic>Western blot</topic><topic>Wild birds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martínez, J.</creatorcontrib><creatorcontrib>Tomás, G.</creatorcontrib><creatorcontrib>Merino, S.</creatorcontrib><creatorcontrib>Arriero, E.</creatorcontrib><creatorcontrib>Moreno, J.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Ecology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Functional ecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martínez, J.</au><au>Tomás, G.</au><au>Merino, S.</au><au>Arriero, E.</au><au>Moreno, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Serum Immunoglobulins in Wild Birds by Direct ELISA: A Methodological Study to Validate the Technique in Different Species Using Antichicken Antibodies</atitle><jtitle>Functional ecology</jtitle><date>2003-10</date><risdate>2003</risdate><volume>17</volume><issue>5</issue><spage>700</spage><epage>706</epage><pages>700-706</pages><issn>0269-8463</issn><eissn>1365-2435</eissn><abstract>1. This study presents an easy protocol to measure the amount of immunoglobulins from the blood serum of different bird species in the wild (Ficedula hypoleuca Pallas, Parus caeruleus L., Lanius meridionalis Temminkck, Lanius collurio L., Athene noctua Scopoli and Falco tinnunculus L.) by direct enzyme-linked immunosorbent assay, ELISA using commercial antichicken antibodies. 2. Additionally, the ELISA technique is validated for detecting serum immunoglobulins by means of other electrophoretic (sodium dodecyl sulphate polyacrylamide gel electrophoresis, SDS-PAGE, and native electrophoresis) and immunological (Western blot) methods. 3. The results by Western blot show that the commercial antibody recognized proteins with apparent molecular weight according to heavy and light chains of immunoglobulins. 4. Both ELISA and Western blot data were correlated, implying that the commercial antibody bound to immunoglobulins and not to other proteins or ELISA plates. Densitometric data achieved by SDS-PAGE and native electrophoresis were only correlated in some species indicating a problem in detecting clearly the heavy and light chains, and γ-globulin fraction, respectively. 5. It is concluded that the proposed protocol is easy to carry out and may be used to detect total serum immunoglobulins from most bird species.</abstract><cop>Oxford, UK</cop><pub>British Ecological Society</pub><doi>10.1046/j.1365-2435.2003.00771.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animal, plant and microbial ecology Antibodies Biological and medical sciences Ecological genetics Ecological immunology Ecology Electrophoresis Enzyme linked immunosorbent assay Fundamental and applied biological sciences. Psychology Gels General aspects. Techniques Human ecology humoral immunity Immunoglobulins Methods and techniques (sampling, tagging, trapping, modelling...) Molecular weight Western blot Wild birds |
title | Detection of Serum Immunoglobulins in Wild Birds by Direct ELISA: A Methodological Study to Validate the Technique in Different Species Using Antichicken Antibodies |
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