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Desmin expression in rhabdomyosarcoma: influence of the desmin clone and immunohistochemical method.

机译:横纹肌肉瘤中结蛋白的表达:结蛋白克隆和免疫组化方法的影响。

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摘要

AIM--To determine which, if any, of five commercially available desmin clones is most reliable at labelling desmin filaments and whether the enhanced polymer one step (EPOS) method of labelling is of any advantage in the routine diagnostic laboratory. METHODS--Thirty four rhabdomyosarcomas from the files at The Hospital for Sick Children, Great Ormond Street, London, were studied. Four different desmin clones, DE-R-11, D33, DE-U-10, and PDE, were applied to each using the conventional extravidin biotin peroxidase method. The D33 clone was also applied using the EPOS method. RESULTS--The EPOS method incorporating D33 persistently scored more cells as desmin positive and was positive in four cases which were negative on staining with the other clones. CONCLUSIONS--The D33 desmin clone used with the EPOS method is more reliable for identifying desmin filaments in tumours than other desmin antibodies tested. Different desmin clones using a routine technique label different rhabdomyosarcoma cells and therefore it is justifiable to use more than one clone.
机译:目的-确定五个市售desmin克隆中的哪个(如果有的话)在标记desmin细丝上最可靠,以及增强型聚合物一步(EPOS)标记方法在常规诊断实验室中是否有任何优势方法-研究了伦敦大奥蒙德街病童医院档案中的34个横纹肌肉瘤。使用常规的抗生物素蛋白生物素过氧化物酶方法,将四个不同的结蛋白克隆DE-R-11,D33,DE-U-10和PDE应用于每个克隆。还使用EPOS方法应用了D33克隆。结果-结合D33的EPOS方法持续获得更多的细胞结蛋白阳性结果,其中4例阳性,其他克隆染色均阴性。结论-与其他测试的desmin抗体相比,与EPOS方法一起使用的D33 desmin克隆在鉴定肿瘤中的desmin细丝方面更可靠。使用常规技术的不同结蛋白克隆标记不同的横纹肌肉瘤细胞,因此使用多个克隆是合理的。

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