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Evaluation of a monoclonal antibody to ras peptide RAP-5 claimed to bind preferentially to cells of infiltrating carcinomas.

机译:对ras肽的单克隆抗体RAP-5的评估声称其优先结合浸润癌的细胞。

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摘要

RAP-5, a monoclonal antibody raised against a p21ras peptide, has been claimed to show immunohistochemical localisation of cells with infiltrative properties in human tumours. We confirmed that this antibody reveals pronounced cellular heterogeneity in human colonic neoplasms but could find no obvious relationship to infiltrative activity. RAP-5 bound to many different cell types, neoplastic and normal. In order to clarify the specificities of RAP-5 we applied it to two cell lines: nontumorigenic hamster fibroblasts in which ras expression is barely detectable, and a vigorously tumorigenic line derived from these fibroblasts by insertion of the human mutated Ha-ras oncogene in a high expression vector. Another antibody to p21ras, Y13-259, clearly distinguished between these cell lines both on immunoblots and immunocytochemically, but RAP-5 did not. Rather, it bound to proteins of a variety of molecular weights in both cell lines. The results show that RAP-5 is unlikely to be a useful reagent for detection of ras associated proteins in human tissues.
机译:RAP-5是一种针对p21ras肽的单克隆抗体,据称可在人体肿瘤中显示具有浸润特性的细胞的免疫组织化学定位。我们证实该抗体在人结肠肿瘤中显示出明显的细胞异质性,但与浸润活性没有明显关系。 RAP-5与许多不同的细胞类型(肿瘤细胞和正常细胞)结合。为了阐明RAP-5的特异性,我们将其应用于两种细胞系:几乎无法检测到ras表达的非致瘤仓鼠成纤维细胞,以及通过将人类突变的Ha-ras致癌基因插入到成纤维细胞中而衍生自这些成纤维细胞的有力致瘤系。高表达载体。 p21ras的另一种抗体Y13-259在免疫印迹和免疫细胞化学上都清楚地区分了这些细胞系,但RAP-5没有。相反,它在两种细胞系中都与多种分子量的蛋白质结合。结果表明,RAP-5不太可能成为检测人体组织中ras相关蛋白的有用试剂。

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