Identification of caprine arthritis-encephalitis retrovirus proteins in immunodiffusion precipitin lines

1 Animal Disease Research Unit, Agricultural Research Service, U.S. Department of Agriculture and the Department of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, Pullman, Washington 99164, U.S.A. Precipitin lines formed between serum from a goat...

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Veröffentlicht in:Journal of general virology 1985-05, Vol.66 (5), p.1139-1143
Hauptverfasser: Adams, D.S, Gogolewski, R.P, Barbet, A.F, Cheevers, W.P
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container_end_page 1143
container_issue 5
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container_title Journal of general virology
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creator Adams, D.S
Gogolewski, R.P
Barbet, A.F
Cheevers, W.P
description 1 Animal Disease Research Unit, Agricultural Research Service, U.S. Department of Agriculture and the Department of Veterinary Microbiology and Pathology, College of Veterinary Medicine, Washington State University, Pullman, Washington 99164, U.S.A. Precipitin lines formed between serum from a goat infected with caprine arthritis-encephalitis virus (CAEV) and radiolabelled viral proteins in polyethylene glycolconcentrated culture medium were excised from immunodiffusion (ID) plates and analysed by polyacrylamide gel electrophoresis. The two major precipitin lines contained the 135000 mol. wt. glycoprotein (gp135) and the internal 28000 mol. wt. structural protein (p28). This method obviates the use of purified proteins or monospecific antisera to positively determine viral constituents in ID precipitin lines formed between a crude antigen preparation and antiserum against whole virus. Keywords: CAEV, serum, proteins Received 12 September 1984; accepted 14 January 1985.
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Precipitin lines formed between serum from a goat infected with caprine arthritis-encephalitis virus (CAEV) and radiolabelled viral proteins in polyethylene glycolconcentrated culture medium were excised from immunodiffusion (ID) plates and analysed by polyacrylamide gel electrophoresis. The two major precipitin lines contained the 135000 mol. wt. glycoprotein (gp135) and the internal 28000 mol. wt. structural protein (p28). This method obviates the use of purified proteins or monospecific antisera to positively determine viral constituents in ID precipitin lines formed between a crude antigen preparation and antiserum against whole virus. 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Precipitin lines formed between serum from a goat infected with caprine arthritis-encephalitis virus (CAEV) and radiolabelled viral proteins in polyethylene glycolconcentrated culture medium were excised from immunodiffusion (ID) plates and analysed by polyacrylamide gel electrophoresis. The two major precipitin lines contained the 135000 mol. wt. glycoprotein (gp135) and the internal 28000 mol. wt. structural protein (p28). This method obviates the use of purified proteins or monospecific antisera to positively determine viral constituents in ID precipitin lines formed between a crude antigen preparation and antiserum against whole virus. 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Psychology</subject><subject>Glycoproteins - analysis</subject><subject>Glycoproteins - immunology</subject><subject>goats</subject><subject>Goats - microbiology</subject><subject>Immunodiffusion</subject><subject>immunodiffusion tests</subject><subject>Microbiology</subject><subject>Molecular Weight</subject><subject>Retroviridae</subject><subject>Retroviridae - analysis</subject><subject>Retroviridae - immunology</subject><subject>Techniques used in virology</subject><subject>Viral Proteins - analysis</subject><subject>Viral Proteins - immunology</subject><subject>Viral Structural Proteins</subject><subject>Virology</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1985</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS1EVYbCL0CILBBiY_A7k2VV8ahUqYvSteXY1xOjxA52AuLf19GMRuxYWdb5zvH1uQi9oeQTJV33mRDGMOW0xUphiSnl3TO0o0JJzKr-HO3OxAv0spSfhFAhZHuJLnnHOJVyh4ZbB3EJPlizhBSb5Btr5hwiNCYvQw5LKBiihXkw43ZpMiw5_Q55Lc2c0wIhlibEJkzTGpML3q9lC5oz2DBXR2zGmlZeoQtvxgKvT-cVevz65cfNd3x3_-325voOW6HYglvjBJfOKNN6cAKk8_2e-M7Y1lFqO8Fb7oh0RBjphAJwnTQ9k31PhHOW8Cv04Zhbh_u1Qln0FIqFcTQR0lp0qyhvBaH_Balgcs8lryA_gjanUjJ4XfuZTP6rKdHbIvRWs95q1kppqbdFVNfbU_zaT-DOnlPzVX9_0k2xZvTZRBvKGdsLRjslKvbxiA3hMPwJGfQB4hTqKH1Iuq7h3xffHVFvkjaHXNMeH1j9KWFKUtYK_gQnBqsM</recordid><startdate>198505</startdate><enddate>198505</enddate><creator>Adams, D.S</creator><creator>Gogolewski, R.P</creator><creator>Barbet, A.F</creator><creator>Cheevers, W.P</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7T7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>198505</creationdate><title>Identification of caprine arthritis-encephalitis retrovirus proteins in immunodiffusion precipitin lines</title><author>Adams, D.S ; Gogolewski, R.P ; Barbet, A.F ; Cheevers, W.P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-7ad435da6a7fed4e5dfb80f9ac7d11c94373d05d04a5d46eed95ab25bb04ddc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1985</creationdate><topic>Animals</topic><topic>Antigens, Viral</topic><topic>arthritis</topic><topic>Arthritis, Infectious - microbiology</topic><topic>Arthritis, Infectious - veterinary</topic><topic>Biological and medical sciences</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>encephalitis</topic><topic>Encephalitis - microbiology</topic><topic>Encephalitis - veterinary</topic><topic>Fundamental and applied biological sciences. 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Precipitin lines formed between serum from a goat infected with caprine arthritis-encephalitis virus (CAEV) and radiolabelled viral proteins in polyethylene glycolconcentrated culture medium were excised from immunodiffusion (ID) plates and analysed by polyacrylamide gel electrophoresis. The two major precipitin lines contained the 135000 mol. wt. glycoprotein (gp135) and the internal 28000 mol. wt. structural protein (p28). This method obviates the use of purified proteins or monospecific antisera to positively determine viral constituents in ID precipitin lines formed between a crude antigen preparation and antiserum against whole virus. Keywords: CAEV, serum, proteins Received 12 September 1984; accepted 14 January 1985.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>3923155</pmid><doi>10.1099/0022-1317-66-5-1139</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Microbiology Society; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Animals
Antigens, Viral
arthritis
Arthritis, Infectious - microbiology
Arthritis, Infectious - veterinary
Biological and medical sciences
Electrophoresis, Polyacrylamide Gel
encephalitis
Encephalitis - microbiology
Encephalitis - veterinary
Fundamental and applied biological sciences. Psychology
Glycoproteins - analysis
Glycoproteins - immunology
goats
Goats - microbiology
Immunodiffusion
immunodiffusion tests
Microbiology
Molecular Weight
Retroviridae
Retroviridae - analysis
Retroviridae - immunology
Techniques used in virology
Viral Proteins - analysis
Viral Proteins - immunology
Viral Structural Proteins
Virology
title Identification of caprine arthritis-encephalitis retrovirus proteins in immunodiffusion precipitin lines
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