EBER in situ hybridization for Epstein-Barr virus.

EBER in situ hybridization for Epstein-Barr virus.
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DOI:
10.1007/978-1-62703-357-2_16
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发表时间:
2013-01-01
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
通讯作者:
Chen, Yuan-Yuan
Chen, Yuan-Yuan
中科院分区:
其他
文献类型:
--
作者:
Weiss, Lawrence M;Chen, Yuan-Yuan

文献摘要

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EB病毒编码区(EBER)原位杂交是检测组织切片中EB病毒(EBV)的首选方法。由于潜伏感染细胞中存在大量EBER拷贝,因此可以使用非同位素方法。阳性研究显示EBV感染细胞的细胞核染色,染色质突出,通常不包括核仁。假阴性结果通常是组织中RNA降解的结果,这一发现可以通过使用聚T探针作为RNA保存的对照来检测。
Epstein-Barr encoding region (EBER) in situ hybridization is the methodology of choice for the detection of the Epstein-Barr virus (EBV) in tissue sections. Because of the large numbers of copies of EBERs present in latently infected cells, non-isotopic methods can be used. Positive studies show staining in the nuclei of the EBV-infected cells, accentuating the chromatin and often excluding the nucleolus. False-negative results are most often the result of RNA degradation in the tissues, a finding that may be detected through the use of a polyT probe as a control for RNA preservation.