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一种新的免疫组化染色方法可以在保存抗体的同时,实现淋巴结微转移的超快速检测。

A novel immunohistochemical staining method allows ultrarapid detection of lymph node micrometastases while conserving antibody.

机构信息

Department of Thoracic Surgery, Akita University Graduate School of Medicine, 1-1-1 Hondo Akita City 010-8543, Japan.

出版信息

Acta Histochem Cytochem. 2011 Jun 29;44(3):133-9. doi: 10.1267/ahc.11006. Epub 2011 Jun 3.

Abstract

We developed a novel ultrarapid immunohistochemical staining method in which an AC electric field is used to facilitate detection of tumor cells. Frozen sections of non-small cell lung cancer in lymph nodes were fixed in acetone for 2 min, after which they were incubated for 2 min with an anti-pancytokeratin antibody cocktail and then with EnVision(TM) complex under an alternating current (AC) electric field. The sections were then incubated with a chromogen (3,3'diaminobenzidine) for 3 min and counterstained with hematoxylin. This method enabled detection of tumor cells in frozen sections in less than 15 min. In addition, we were able to reduce the amount of antibody used by more than 90% when the sections were incubated under the AC electric field for a longer period. This method could be a useful tool for frozen section diagnosis and research. Furthermore, with this method the cost of immunohistochemical staining can be reduced.

摘要

我们开发了一种新颖的超快免疫组织化学染色方法,该方法利用交流电场促进肿瘤细胞的检测。将非小细胞肺癌的淋巴结冷冻切片用丙酮固定 2 分钟,然后用抗泛细胞角蛋白抗体鸡尾酒孵育 2 分钟,然后在交流电场下孵育 EnVision(TM)复合物。然后将切片用显色剂(3,3'-二氨基联苯胺)孵育 3 分钟,并用苏木精复染。该方法可使冷冻切片中的肿瘤细胞在不到 15 分钟的时间内被检测到。此外,当将切片在交流电场中孵育更长时间时,我们能够将抗体的使用量减少 90%以上。该方法可能是冷冻切片诊断和研究的有用工具。此外,通过这种方法可以降低免疫组织化学染色的成本。

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