E. Reytor et al., A competitive enzyme linked immunosorbent assay for recombinant Bm86 produced in Pichia pastoris, BIOTECH TEC, 12(12), 1998, pp. 919-923
A competitive enzyme linked immonosorbent assay (ELISA) was developed for q
uantification of recombinant Bm86 protein (rBm86), antigen of the vaccine G
avac(TM) against the cattle tick Boophilus microplus. Monoclonal antibody (
Mab) SSBm1 showed identical recognition to folded and denatured antigen and
was used in the competition assay. This ELISA was sensitive enough to dete
ct 60 ng/ml of rBm86. Within-assay coefficient of variation was 5.7 to 6.2
% and between-assay variation was 7.7 to 11.6 %. The level of expression of
recombinant Bm86 in Pichia pastoris reached about 2.7 g per liter of cultu
re after 80 hour of fermentation.