Cj. Munro et al., ELISA FOR THE MEASUREMENT OF SERUM AND URINARY CHORIONIC-GONADOTROPINCONCENTRATIONS IN THE LABORATORY MACAQUE, American journal of primatology, 41(4), 1997, pp. 307-322
A rapid, sensitive, enzyme-linked immunosorbant assay (ELISA) for the
measurement of chorionic gonadotropin (CG) in serum and urine samples
of laboratory macaques is reported. The ligand (CG) is captured by a r
eadily available, widely used, and well-characterized monoclonal antib
ody (Mab, 518B7) generated against the beta subunit of bovine luteiniz
ing hormone (LH). This Mab, while specific for LH, shows very little s
pecies specificity, and has been shown to detect LH and CG by radioimm
unoassay (RIA) in both human and non-human primates. A polyclonal anti
serum raised in rabbits against human chorionic gonadotropin (hCG) is
conjugated to horseradish peroxidase, and is used as the second antibo
dy signal. This anti-hCG antiserum cross reacts with CG secreted by bo
th the human (hCG) and macaque (mCG). The ELISA utilizes hCG as the st
andard, and results are based on the relative concentrations of mCG in
serum and urine. Total assay time is less than 5 hours. Range of the
standard curve is 0.002 to 0.5 ng hCG/well, and the least detectable c
oncentration of hCG is 0.0023 +/- 0.0007 ng/well. Pregnancy was detect
ed in early pregnant macaques (M. fascicularis) on 9 (N = 1/16), 10 (N
= 1/16), 11 (N = 1/16), 12 (N = 6/16), 13 (N = 1/16), 14 (N = 4/16),
and 15 (N = 2/16) days following the pre-ovulatory urinary estrone con
jugate peak. The detection of pregnancy by urinary mCG occurred approx
imately 24 to 72 hours after its detection in serum. (C) 1997 Wiley-Li
ss, Inc.