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从传染性支气管炎病毒分离株制备血凝抗原。

Preparing hemagglutinating antigen from isolates of infectious bronchitis virus.

作者信息

Lashgari M S, Newman J A

出版信息

Avian Dis. 1982 Jul-Sep;26(3):508-19.

PMID:6293442
Abstract

The hemagglutinating (HA) activity of 14 strains of infectious bronchitis virus (IBV) was investigated. The optimal conditions for IBV antigen preparation include inoculation of 10- or 11-day-old specific pathogen-free embryonated eggs and incubation for 30 hours at 37 C. Embryos were inoculated via the allantoic cavity with 0.1 ml of a low embryonic passage of the virus (10(7) to 10(8) EID50/ml). Allantoic fluid was harvested and pooled, and a 100-fold concentration of virus particles was achieved by centrifugation for 3 hours at 30,000 x g. Virus pellets were resuspended in Tris-hydrochloride buffer containing 3 units of phospholipase-C (type-1) enzyme/ml and incubated for 2 hours at 37 C. All IBV strains tested demonstrated positive HA activity with chicken red blood cells. The antigen was stored in liquid state or lyophilized at 4 C.

摘要

对14株传染性支气管炎病毒(IBV)的血凝(HA)活性进行了研究。制备IBV抗原的最佳条件包括接种10或11日龄无特定病原体的鸡胚,并在37℃孵育30小时。通过尿囊腔向胚胎接种0.1 ml低代次病毒(10⁷至10⁸ EID₅₀/ml)。收集并合并尿囊液,通过在30000×g下离心3小时使病毒颗粒浓度提高100倍。将病毒沉淀重悬于含有3单位磷脂酶C(1型)酶/ml的 Tris-盐酸缓冲液中,并在37℃孵育2小时。所有测试的IBV毒株对鸡红细胞均表现出阳性HA活性。抗原以液态储存或在4℃冻干。

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