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抗山羊ΔfosB基因表达产物抗体的制备及应用
引用本文:郑惠玲,祝珍珍,安俊辉,杨振宇,邢瑞芳,闫林慧.抗山羊ΔfosB基因表达产物抗体的制备及应用[J].生物工程学报,2010,26(12):1704-1709.
作者姓名:郑惠玲  祝珍珍  安俊辉  杨振宇  邢瑞芳  闫林慧
作者单位:西北农林科技大学动物科技学院,杨凌,712100
基金项目:西北农林科技大学基本科研业务费 (No. Z109021002),农业部公益性行业科研专项 (农业) 经费 (No. 3-45) 资助。
摘    要:ΔfosB是fosB基因的自然截短型,稳定存在于许多组织中,在脂肪细胞和成骨细胞的形成和分化中起到重要作用。ΔFosB蛋白可能与钙在骨和乳腺中的代谢有关,并且调控钙从骨向乳腺转移的信号通路。将奶山羊的ΔfosB基因亚克隆到pET32a载体得到pET32a-ΔfosB原核表达载体,IPTG诱导其在大肠杆菌中表达,纯化融合蛋白免疫兔子制备多克隆抗体。ELISA检测显示抗体效价达1:51200,Western blotting结果显示制备的抗体能特异性检测原核表达的ΔFosB蛋白以及在HEK-293细胞中表达的ΔFosB蛋白。进一步的组织差异表达检测表明ΔFosB在山羊的乳腺、骨髓、脑髓、肌肉、心脏、肝和肺组织中均有表达。

关 键 词:山羊,ΔFosB,原核表达,多克隆抗体,组织差异表达
收稿时间:2010/3/30 0:00:00

Preparation and application of goat deltafosB gene expression product antibody
Huiling Zheng,Zhenzhen Zhu,Junhui An,Zhenyu Yang,Ruifang Xing and Linhui Yan.Preparation and application of goat deltafosB gene expression product antibody[J].Chinese Journal of Biotechnology,2010,26(12):1704-1709.
Authors:Huiling Zheng  Zhenzhen Zhu  Junhui An  Zhenyu Yang  Ruifang Xing and Linhui Yan
Institution:College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China;College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China;College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China;College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China;College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China;College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China
Abstract:deltaFosB, a naturally occurring truncated isform of fosB gene, existed in many tissues stably and played an important role in formation and differentiation of adipocyte and osteoblast. deltaFosB may be related to the metabolism of calcium in bone and mammary gland and regulate the signal pathway of calcium transfer from bone to mammary gland. We first sub-cloned deltafosB gene of goat into the vector pET32a to construct prokaryotic expression vector pET32a-deltafosB. Then we induced for deltafosB gene expression efficiently by IPTG. Finally we immunized the adult rabbits with purified recombinant deltaFosB to prepare rabbit anti-goat deltaFosB polyclonal antibody. iELISA analysis showed the antibody with the titer of 1:51 200, and Western blotting result showed that the antibody could specifically detect the deltaFosB protein expressed in prokaryotic cell and HEK-293 cell, respectively. Further Western blotting assay showed that deltaFosB expressed in various tissues of goat in vivo.
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