Practical procedure for enzyme immunoassay of progesterone in bovine serum [cattle, rabbit, goat, radioimmunoassay]
1980
Nakaeo, T. (Rakuno Gakuen Univ., Ebetsu-shi, Hokkaido (Japan). Coll. of Dairying)
An enzyme immunoassay of progesterone was established by using beta-galactosidase from E. coli as a label. The enzyme was conjugated with 11alpha-hydroxyprogesterone-hemisuccinate using water-soluble carbodimide. Rabbit antiserum to 11alpha-hydroxyprogesterone-hemisuccinate-bovine serum albumin was previously obtained and anti-rabbit gamma globulin goat serum was used as second antibody. The enzyme activity was measured by utilizing hydrolysis of O-nitrophenyl-beta-D-galactopyranoside. The least detectable concentration of progesterone was 12 pg per tube. The measurable range of progesterone in 0.1 ml of bovine serum was between 1.25 ng/ml and 10 ng/ml. This method satisfied the general criteria regarding specifity, precision and recovery rate. Correlation between the progesterone levels determined by enzyme immunoassay and radioimmunoassay was quite high (r = 0.99, P or
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