中文摘要：

目的制备兔抗人同源异形盒基因HOXB9的多克隆抗体，为后续深入研究HOXB9蛋白的功能提供工具。方法采用聚合酶链反应（PCR）和DNA重组技术，构建HOXB9基因5’端7-458碱基片段到原核表达载体pGEX-4T-1和pMal-C2x中，热休克法转化及异丙基-B—D-硫代吡喃半乳糖苷诱导表达谷胱甘肽转移酶标签的HOXB9N端融合蛋白和麦芽糖结合蛋白标签的HOXB9N端融合蛋白。纯化GST—HOXB9N端融合蛋白免疫新西兰白兔，ELISA鉴定效价后，颈动脉放血，收集血清，纯化抗体。免疫印迹法及免疫沉淀法鉴定抗体有效性及特异性。结果本实验制备的抗体能够特异识别目标分子的单-条带，并且具有较强的免疫沉淀天然构象的HOXB9蛋白的能力；采用所制备的抗体检测发现，HOXB9蛋白在小鼠免疫器官、胰脏、结肠、肺、小脑、雌性生殖系统及睾丸中表达较高，其他器官表达较低或无表达。结论成功制备了特异而有效的兔抗人HOXB9蛋白多克隆抗体，此多克隆抗体可用于免疫印迹法分析及免疫沉淀实验。

英文摘要：

Objective The purpose of this study was to prepare rabbit anti-homeobox B9 （HOXB9） polyclonal antibody and to provide a tool for future study. Methods DNA fragments of human HOXB9 gene 5＇terminal 7-458 base pairs was respectively cloned into PGEX-4T-1 vector expressing GST tag and pMal-C2x vector expressing MBP tag by polymerasechain reaction and recombinant DNA technology. The GST-HOXB9-N-terminal fusion protein and MBP-HOXB9- N-terminal fusion protein were expressed by E. coli BL21 （ DE3 ） after heat shock transformation and IPTG induction. The New Zealand rabbit was immunized with the purified GST-HOXB9-N-terminal fusion protein. We used ELISA assay to determine the tiler of the antiserum. If the antiserum was effective, the rabbit blood was obtained from the carotid artery and immunoglobulinG（IgG） was purified from serum. Effectiveness and specificity of the antibody were identified by Western blotting and immunoprecipitation. Results The prepared antibody specifically recognized a single band of the target molecule, and had a strong capability of immunoprecipitation on the native HOXB9 protein. Using this antibody, we demonstrated that HOXB9 expressed highly in the mouse immune organs, pancreas, colon, lung, cerebellum, female reproductive system and testis,while expressed lowly in other organs. Conclusion We successfully prepared a rabbit anti- human HOXB9 polyclonal antibody. This polyclonal antibody is specific and effective, and may be used for Western blotting and immunoprecipitation analysis.