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BMC Vet Res. 2012; 8: 91.
Published online 2012 June 26. doi:  10.1186/1746-6148-8-91
PMCID: PMC3413586
The complement system of the goat: Haemolytic assays and isolation of major proteins
Isabel Moreno-Indias,1,2 Alister W Dodds,2 Anastasio Argüello,corresponding author1 Noemi Castro,1 and Robert B Sim2
1Animal Science Department, Universidad de las Palmas de Gran Canaria, Arucas, Las Palmas, 35413, Spain
2MRC Immunochemistry Unit, Department of Biochemistry, University of Oxford, South Parks Road, Oxford, OX1 3QU, UK
corresponding authorCorresponding author.
Isabel Moreno-Indias: imoreno/at/becarios.ulpgc.es; Alister W Dodds: awdodds/at/googlemail.com; Anastasio Argüello: aarguello/at/dpat.ulpgc.es; Noemi Castro: ncastro/at/dpat.ulpgc.es; Robert B Sim: bob.sim/at/bioch.ox.ac.uk
Received August 30, 2011; Accepted June 26, 2012.
Abstract
Background
The aim of the present study was to develop a haemolytic assay for the study of the complement system in dairy goats (Capra aegagrus hircus) and to characterize the major goat complement system proteins.
Results
The commonly used sheep erythrocyte sensitized with rabbit antibodies were not sensitive to lysis by goat serum, but the combination of human red blood cells (RBC) plus rabbit antibodies was the best option found for goat complement assay. A buffer based on HEPES instead of the classical veronal (barbitone) was developed. Three proteins were isolated: factor H, C1q and C3 and these were compared with the corresponding human proteins. A novel affinity chromatography technique was developed for isolation of factor H.
Conclusions
Human RBC plus rabbit antibodies were a suitable option for haemolytic assays. The isolated proteins are similar to the human counterparts.
Keywords: Goat, Complement system, C3, C1q, Factor H
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