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首页> 外文期刊>Hybridoma >Generation of monoclonal antibodies against human recombinant interferon beta using genetic immunization with simultaneous expression of IgM and IgG isotypes.
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Generation of monoclonal antibodies against human recombinant interferon beta using genetic immunization with simultaneous expression of IgM and IgG isotypes.

机译:使用同时表达IgM和IgG同种型的基因免疫产生针对人重组干扰素β的单克隆抗体。

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摘要

Monoclonal antibodies (MAbs) against human recombinant interferon beta (hrIFNbeta) were generated by genetic immunization (GI). In order to test two viral promoters frequently used in mammalian expression plasmid vectors, mice were inoculated four times by intramuscular injection, without adjuvant, with 100 microg of either pcDNA 3.1hrIFNbeta or pZeoSV2IFNbeta containing the entire human interferon beta gene and under the control of, respectively, human cytomegalovirus (HCMV) immediate-early promoter or early SV-40 enhancer/promoter. Only serum samples from mice immunized with pZeoSV2IFNbeta were positive to anti-hrIFNbeta. The spleens of the immunized mice were fused with myeloma Sp2/0 cells and the hybridoma clones generated screened by an in house enzyme-linked immunosorbent assay (ELISA). Fourteen MAbs were selected as reactive with hrIFNbeta. Western blot analysis was performed and only one recognized the 18 kDa isoform (non-glycosylated) of hrIFNbeta. All MAbs were subjected to antibody isotype characterization with a commercial ELISA and showed unusual profile with simultaneous expression of both IgM and IgG2a isotypes. This observation is further supported by RT-PCR amplification of the IgM CH4 domain using total RNA from hybridomas.
机译:通过基因免疫(GI)产生了针对人类重组干扰素β(hrIFNbeta)的单克隆抗体(MAb)。为了测试哺乳动物表达质粒载体中常用的两种病毒启动子,在无佐剂的情况下,通过肌肉内注射小鼠将小鼠接种四次,每次100μg含有完整人干扰素β基因的pcDNA 3.1hrIFNbeta或pZeoSV2IFNbeta,人巨细胞病毒(HCMV)立即早期启动子或早期SV-40增强子/启动子。只有来自用pZeoSV2IFNbeta免疫的小鼠的血清样品对抗hrIFNbeta呈阳性。将免疫小鼠的脾脏与骨髓瘤Sp2 / 0细胞融合,并通过室内酶联免疫吸附测定(ELISA)筛选产生的杂交瘤克隆。选择十四个MAb与hrIFNβ反应。进行了蛋白质印迹分析,只有一个人识别了hrIFNβ的18 kDa亚型(非糖基化)。所有的单克隆抗体都通过商业ELISA进行了抗体同种型鉴定,并显示出异常的特征,同时表达IgM和IgG2a同种型。使用杂交瘤中的总RNA对IgM CH4域进行RT-PCR扩增,进一步支持了这一观察结果。

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