A SENSITIVE AND SPECIFIC 2-SITE, SANDWICH-AMPLIFIED ENZYME-IMMUNOASSAY FOR NEUROPEPTIDE-Y

被引:44
作者
GROUZMANN, E
AUBERT, JF
WAEBER, B
BRUNNER, HR
机构
[1] UNIV HOSP LAUSANNE, DIV HYPERTENS, LAUSANNE, SWITZERLAND
[2] UNIV HOSP LAUSANNE, CARDIOVASC RES GRP, LAUSANNE, SWITZERLAND
关键词
AMPLIFIED ENZYME IMMUNOASSAY; NEUROPEPTIDE-Y; MONOCLONAL ANTIBODY;
D O I
10.1016/0196-9781(92)90004-M
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of a new enzyme immunoassay for neuropeptide Y (NPY) is reported. Two monoclonal antibodies directed against distinct epitopes of NPY are used, one as a capture antibody (NPY02) and the other one as an indicator antibody (NPY05), this latter antibody being labeled with alkaline phosphatase. The assay calibration curve was performed over concentrations of 1 to 250 pM in a NPY-free plasma. The intra-assay coefficient of variation (CV) ranged from 0.025 to 11.9%, whereas the interassay CV was comprised between 5 and 12%. The limit of detection of this assay was 1 pM (100 amol/well). Neuropeptide Y levels are related to sampling conditions; basal concentrations of NPY with low SEM are found when less than 1.2 ml of blood is taken in EDTA tubes. the sample is centrifuged at 4-degrees-C, and immediately frozen. Unanesthetized spontaneously hypertensive rats exhibited higher NPY plasma concentrations than normotensive Wistar-Kyoto controls (53 +/- 7 pM and 25 +/- 2 pM, respectively. mean +/- SEM. p < 0.01). Plasma NPY levels are similar in 16- and 36-week-old animals. In conclusion, this technique makes it possible to assay a large number of samples within 24 h without requiring radioactivity.
引用
收藏
页码:1049 / 1054
页数:6
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