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抗hARD1抗血清制备及其初步肿瘤免疫组化分析
引用本文:余敏,黄超,向明钧,赖建华,杨慧,马明星,谭德勇.抗hARD1抗血清制备及其初步肿瘤免疫组化分析[J].生物工程学报,2008,24(7):1155-1161.
作者姓名:余敏  黄超  向明钧  赖建华  杨慧  马明星  谭德勇
作者单位:云南大学生命科学学院生物化学与分子生物学实验室,昆明,650091
基金项目:国家自然科学基金(Nos. 30360040, 30760057), 云南省科技厅攻关项目(No. 2006SG09)资助。
摘    要:人ARD1(human arrest defective 1, hARD1)基因被确定具有N-乙酰基转移酶活性, 但其生理学功能并不清楚。为了探讨hARD1基因与肿瘤的关系, 检测hARD1蛋白在不同肿瘤中的表达, 克隆了hARD1基因并进行原核表达, 利用镍离子螯合(His-bind)柱层析纯化, 得到纯度达95%以上的hARD1蛋白。以纯化的重组蛋白免疫小鼠, 制备了抗hARD1蛋白的抗血清。利用抗hARD1多抗血清检测常见的临床肿瘤病理组织, 发现hARD1蛋白在乳腺肿瘤、前列腺癌, 以及肺癌中有较高频率的表达, 其中乳腺肿瘤中的表达频率最高, 达到70%, 远高于其他肿瘤组织。表明hARD1蛋白的高表达可能是乳腺肿瘤组织的一个标志, 为进一步揭示hARD1与乳腺肿瘤的关系奠定了基础。

关 键 词:hARD1基因    免疫组化分析    肿瘤
收稿时间:12 November 2007

hARD1 Antiserum Preparation and Primary Immunohistochemical Analysis of hARD1 in Tumor Tissues
Min Yu,Chao Huang,Mingjun Xiang,Jianhua Lai,Hui Yang,Mingxing Ma and Deyong Tan.hARD1 Antiserum Preparation and Primary Immunohistochemical Analysis of hARD1 in Tumor Tissues[J].Chinese Journal of Biotechnology,2008,24(7):1155-1161.
Authors:Min Yu  Chao Huang  Mingjun Xiang  Jianhua Lai  Hui Yang  Mingxing Ma and Deyong Tan
Institution:Laboratory of Biochemistry and Molecular Biology, School of Life Science, Yunnan University, Kunming 650091, China;Laboratory of Biochemistry and Molecular Biology, School of Life Science, Yunnan University, Kunming 650091, China;Laboratory of Biochemistry and Molecular Biology, School of Life Science, Yunnan University, Kunming 650091, China;Laboratory of Biochemistry and Molecular Biology, School of Life Science, Yunnan University, Kunming 650091, China;Department of Pathology, First Peoples Hospital of Yunnan Province, Kunming 650032, China;Laboratory of Biochemistry and Molecular Biology, School of Life Science, Yunnan University, Kunming 650091, China;Laboratory of Biochemistry and Molecular Biology, School of Life Science, Yunnan University, Kunming 650091, China
Abstract:Human arrest defective 1(hARD1) is an acetyltransferase; its physiological significance remains unclear. To explore the relationship between ARD1 protein and tumors, we detected the hARD1 protein in tumor tissues in vivo. We cloned hARD1 gene from Hela cell and construct recombinant plasmid pET28b-hARD1. The recombinant plasmid was transformed into E. coli BL21(DE3)plysS. hARD1 protein was expressed by inducing with IPTG(1 mmol/L) and purified up to 95% through Ni2+ chelation affinity chromatography. We used the purified hARD1 protein as antigen immunized the Balb/c mice and obtained the hARD1 specific polyclonal antiserum. Through immunohistochemical analysis of different tumor tissues in vivo, we found that hARD1 expressed at high frequency in breast cancer, prostate cancer and lung cancer, especially, hARD1 expression frequency in breast cancer was up to 70%, which is higher than in the other tumors. These results indicate that the high expression level of hARD1 could be an indicator of the breast cancer. This new finding would be a foundation to further explore the relationship between breast tumor and hARD1.
Keywords:hARD1 gene  immunohistochemical analysis  tumors
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