免疫组织化学
表位
抗原回收
多克隆抗体
单克隆抗体
抗原
生物素化
抗体
表位定位
链霉亲和素
亲和素
蛋白水解酶
化学
生物素
分子生物学
生物
计算生物学
酶
生物化学
免疫学
作者
Amanda F. Marsch,Jonathan Truong,Melissa M. McPherson,Jacqueline M. Junkins‐Hopkins,Dirk M. Elston
出处
期刊:American Journal of Dermatopathology
[Ovid Technologies (Wolters Kluwer)]
日期:2015-07-21
卷期号:37 (8): 593-603
被引量:5
标识
DOI:10.1097/dad.0000000000000335
摘要
Immunohistochemistry (IHC) is a method by which specific target antigens can be detected in formalin-fixed paraffin-embedded tissue and involves the use of monoclonal or polyclonal antibodies; visualization of specific tissue antigens is achieved through an enzymatic reaction that transforms a colorless chromogen to a colored one. These enzymes may be attached to the antibody through a protein–ligand method (eg, biotin–avidin or biotin–streptavidin) or through a secondary antibody. Epitopes that are masked by protein linkage during formalin fixation are unmasked using a retrieval system that either uses heat (heat-induced epitope retrieval) or proteolytic enzymes (proteolytic-induced epitope retrieval). Part 1 of this review will focus and elaborate on the available methodologies for IHC testing, common problems inherent to each technique, and how they can be resolved. Part 2 will focus on common problems and artifacts encountered during IHC staining, likely causes, and methods for addressing each problem.
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