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使用非放射性探针进行组织印迹杂交以检测传染性法氏囊病病毒。

Tissue-print hybridization using a non-radioactive probe for the detection of infectious bursal disease virus.

作者信息

Hathcock T L, Giambrone J J

机构信息

Department of Pathobiology, College of Veterinary Medicine, Auburn University, Alabama 36849-5519.

出版信息

Avian Dis. 1992 Apr-Jun;36(2):202-5.

PMID:1320859
Abstract

Tissue-print hybridization was evaluated as a simplified means for detection of infectious bursal disease virus (IBDV) in the bursa of Fabricius from infected chickens. The assay employed a biotin-labeled synthetic oligonucleotide as a probe. The bound probe was detected using a color assay consisting of streptavidin conjugated to alkaline phosphatase. Bursae were imprinted onto nitrocellulose and then hybridized with the biotinylated probe. Bursal prints from IBDV-infected chickens were readily distinguished from control prints by color development and differences in signal intensity.

摘要

组织印迹杂交被评估为一种用于检测感染鸡法氏囊中传染性法氏囊病病毒(IBDV)的简化方法。该检测采用生物素标记的合成寡核苷酸作为探针。使用由与碱性磷酸酶偶联的链霉亲和素组成的显色测定法检测结合的探针。将法氏囊印在硝酸纤维素上,然后与生物素化探针杂交。通过显色和信号强度差异,很容易将感染IBDV的鸡的法氏囊印迹与对照印迹区分开来。

相似文献

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Double-antibody sandwich ELISA for detection of infectious bursal disease virus.
Br Vet J. 1991 May-Jun;147(3):251-5. doi: 10.1016/0007-1935(91)90049-S.

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