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冷冻切片超快速免疫染色方案。

Protocol for ultrarapid immunostaining of frozen sections.

作者信息

Richter T, Nährig J, Komminoth P, Kowolik J, Werner M

机构信息

Institute of Pathology, Technical University Munich, Germany.

出版信息

J Clin Pathol. 1999 Jun;52(6):461-3. doi: 10.1136/jcp.52.6.461.

Abstract

Rapid immunostaining of frozen sections within a tolerable time span would be very helpful for intraoperative diagnosis. A protocol was therefore established using the enhanced polymer one-step staining (EPOS) system (Dako) with antibodies against leucocyte common antigen (LCA), cytokeratin (CK), and anti-melanoma (MEL). Best results with reliable and specific immunostaining and a labelling intensity comparable to standard immunostaining protocols were achieved with fixation of samples in 100% acetone for 20 seconds (CK, LCA) or two minutes (MEL), followed by incubation of the primary antibody and development of the chromogen reaction with 3,3'diaminobenzidine (DAB) for three and five minutes at 37 degrees C, respectively. The total procedure takes only 12 minutes, thus enabling rapid immunostaining on intraoperative frozen sections. Apart from its use in tumour classification, this method is especially useful in detecting tumour cells in sentinel lymph nodes.

摘要

在可耐受的时间范围内对冰冻切片进行快速免疫染色,对术中诊断非常有帮助。因此,建立了一种方案,使用增强聚合物一步染色(EPOS)系统(达科公司),以及针对白细胞共同抗原(LCA)、细胞角蛋白(CK)和抗黑色素瘤(MEL)的抗体。通过将样本在100%丙酮中固定20秒(CK、LCA)或两分钟(MEL),然后分别在37摄氏度下孵育一抗并用3,3'-二氨基联苯胺(DAB)进行显色反应3分钟和5分钟,获得了可靠且特异的免疫染色以及与标准免疫染色方案相当的标记强度的最佳结果。整个过程仅需12分钟,从而能够在术中冰冻切片上进行快速免疫染色。除了用于肿瘤分类外,该方法在检测前哨淋巴结中的肿瘤细胞方面特别有用。

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