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对人类结肠组织中全长APC基因产物的存在与否进行免疫检测。

Immunodetection of the presence or absence of full-length APC gene product in human colonic tissues.

作者信息

Chop A M, Abraham C L, Adrian T E, Murphy R, Boman B M

机构信息

Creighton Cancer Center, Creighton University School of Medicine, Omaha, NE 68178, USA.

出版信息

Anticancer Res. 1995 May-Jun;15(3):991-7.

PMID:7645991
Abstract

In order to detect the presence or absence of wild-type adenomatous polyposis coli (APC) gene protein (APC) in human colonic tissues, we immunoaffinity purified two polyclonal rabbit antibodies (APC-1 and APC-2) directed against defined epitopes in the middle and carboxyl regions of APC. Such antibodies proved useful in western blot analysis of matched colonic mucosa and tumor sample pairs. A 300 kDa band corresponding to APC was detected in samples from normal colonic mucosa using both antibodies. No tumor samples (n = 14) showed a detectable 300 kDa band. SW480 colon carcinoma cells, known to express truncated APC lacking the carboxyl half of the protein, were also negative. These results indicate that our antibodies bind to full-length but not truncated APC. Thus, western blot analysis employing APC-1 and APC-2 antibodies may be used to evaluate the absence or presence of wild-type APC. The value of this methodology in detecting APC mutations, which mainly involve protein truncation or allelic loss, is based on its ability to demonstrate negative or reduced level of immunoreactivity toward full-length APC in tissues that contain such mutations.

摘要

为了检测人类结肠组织中野生型腺瘤性息肉病基因蛋白(APC)的有无,我们通过免疫亲和法纯化了两种针对APC中部和羧基区域特定表位的兔多克隆抗体(APC-1和APC-2)。这些抗体在配对的结肠黏膜和肿瘤样本对的蛋白质印迹分析中证明是有用的。使用这两种抗体在正常结肠黏膜样本中均检测到一条对应于APC的300 kDa条带。没有肿瘤样本(n = 14)显示出可检测到的300 kDa条带。已知表达缺少蛋白质羧基末端的截短型APC的SW480结肠癌细胞也呈阴性。这些结果表明,我们的抗体与全长APC结合,但不与截短型APC结合。因此,采用APC-1和APC-2抗体的蛋白质印迹分析可用于评估野生型APC的有无。该方法在检测主要涉及蛋白质截短或等位基因缺失的APC突变中的价值,基于其在含有此类突变的组织中对全长APC的免疫反应性呈阴性或降低水平的证明能力。

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