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用于定量测定马血清淀粉样蛋白A的夹心酶联免疫吸附测定法。

Sandwich enzyme-linked immunosorbent assay for quantitative measurement of serum amyloid A protein in horses.

作者信息

Satoh M, Fujinaga T, Okumura M, Hagio M

机构信息

Department of Veterinary Clinical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.

出版信息

Am J Vet Res. 1995 Oct;56(10):1286-91.

PMID:8928944
Abstract

To measure the concentration of serum amyloid A (sAA) protein in horses, a sensitive and highly reproducible sandwich (ELISA) was established, using affinity purified SAA antibody. Results of the ELISA were found to have a high correlation (r = 0.95) with those of the single radial immunodiffusion test. Equine SAA concentration was measured by use of this ELISA. In clinically normal horses, the concentration of SAA was high immediately after birth to 2 weeks of age. After that, SAA concentration had periodic fluctuations in the range of approximately 1.0 to 30 micrograms/ml. Mean (+/- SD)) concentrations of SAA in foals (< or = 12 months old) and adult horses (> or = 18 months old) were 21.23 +/- 12.20 and 14.93 +/- 9.07 micrograms/ml, respectively. In mares during the perinatal period, SAA concentration remained stable within the reference range before parturition. It increased quickly after delivery, and reached a peak value of 101.29 +/- 98.82 micrograms/ml on postpartum day 3, then began to decrease, at postpartum week 2, to the reference range by the end of postpartum month 1. In horses with experimentally induced inflammation, SAA concentration increased quickly and reached approximately four- to 40-fold increase over the pretreatment value on day 1 and remained high on days 2 to 6 after treatment. It then returned to the baseline value by 2 to 4 weeks in association with disappearance of local signs of inflammation. The SAA concentration was high in most horses with clinical signs of inflammation. It was concluded from these data that this ELISA is sensitive and reliable for measuring SAA in horses.

摘要

为测定马血清淀粉样蛋白A(sAA)的浓度,使用亲和纯化的SAA抗体建立了一种灵敏且高度可重复的夹心酶联免疫吸附测定法(ELISA)。发现ELISA结果与单向放射免疫扩散试验结果具有高度相关性(r = 0.95)。使用该ELISA测定马的SAA浓度。在临床正常的马中,出生后至2周龄时SAA浓度较高。此后,SAA浓度在约1.0至30微克/毫升范围内呈周期性波动。驹(≤12个月龄)和成年马(≥18个月龄)的SAA平均(±标准差)浓度分别为21.23±12.20和14.93±9.07微克/毫升。围产期母马在分娩前SAA浓度在参考范围内保持稳定。分娩后迅速升高,在产后第3天达到峰值101.29±98.82微克/毫升,然后开始下降,在产后第2周降至参考范围内,至产后第1个月末恢复正常。在实验性诱导炎症的马中,SAA浓度迅速升高,在治疗后第1天比治疗前值增加约4至40倍,并在治疗后第2至6天保持高水平。然后在2至4周内恢复到基线值,同时局部炎症体征消失。大多数有炎症临床体征的马SAA浓度较高。从这些数据得出结论,该ELISA对于测定马的SAA灵敏且可靠。

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