A spectrophotometric method for the analysis of fenclorac and its metabolite, 3-chloro-4-cyclohexylbenzeneglycolic acid, in human serum was developed. The parent compound represented at least 90% of the total species present in blood; the metabolite was present to the extent of about 10%, primarily
Quantitative determination of titers of anti-zona serum
β Scribed by Tsunoda, Y. ;Sugie, T. ;Mori, J.
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 401 KB
- Volume
- 207
- Category
- Article
- ISSN
- 0022-104X
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β¦ Synopsis
Abstract
The titers of rabbit antiserum against isolated mouse zonae pellucidae were examined by several methods in connection with inhibitory effect on fertilization.
The titers determined by zona precipitate, zona dissolution, indirect immunofluorescence and in vitro fertilization tests were 2^4^, 2^1^ to 2^4^, 2^7^ and 2^4^, respectively. Cytotoxic effect could not be detected from zona antibody. The indirect immunofluorescence was most sensitive for detection of zona antibody but did not represent the extent of inhibitory effect on fertilization. The titer obtained by zona precipitate test was most close to the titer obtained by inhibitory effect on in vitro fertilization.
The present study also demonstrated that at least 0.0375 ml of antiserum per female mouse, equivalent to 0.15β0.25% of body weight, was necessary for inhibition of fertilization in vivo by passive immunization with antiβzona serum.
π SIMILAR VOLUMES
## Abstract Biochemically purified and F(abβ²)~2~ immunoglobulin fractions were prepared from several antisera, including a human serum, which contained antiβzona pellucida activity. Antizona activity was monitored either by the formation of the antibody produced precipitation layer on the zona foll
We have evaluated a new latex nephelometric test for the quantitation of myoglobin in human serum. The assay consists of incubating the diluted serum sample (20-fold) for 12 min at room temperature with latex particles covalently coated with anti-myoglobin antibodies and then quantifying the change