首页> 外文期刊>Journal of Parasitology >Detection of Cryptosporidium parvum oocysts by dot-blotting using monoclonal antibodies to Cryptosporidium parvum virus 40-kDa capsid protein.
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Detection of Cryptosporidium parvum oocysts by dot-blotting using monoclonal antibodies to Cryptosporidium parvum virus 40-kDa capsid protein.

机译:使用小隐隐孢子虫病毒40 kDa衣壳蛋白的单克隆抗体通过斑点印迹检测小隐隐孢子虫卵囊。

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摘要

Monoclonal antibodies (MAb) were prepared against the 40-kDa capsid protein of Cryptosporidium parvum virus (CPV) by immunizing mice with purified recombinant CPV40 protein. In immunoblotting analysis, MAbCPV40-1 bound to a 40-kDa protein in extracts of C. parvum oocysts. This 40-kDa protein was localized in the sporozoite cytoplasm by immunofluorescence (IFA) staining with MAbCPV40-1. In a dot-blot assay, MAbCPV40-1 was capable of detecting 10(2) non-bleach-treated and 10(2)-10(3) bleach-treated C. parvum oocysts. MAbCPV40-1 was capable of detecting CPV40 antigen in both soluble and total C. parvum oocyst protein extracts, indicating a potential use for detecting this parasite in environmental samples.
机译:通过用纯化的重组CPV40蛋白免疫小鼠,制备了针对小隐隐孢子虫病毒(CPV)的40 kDa衣壳蛋白的单克隆抗体(MAb)。在免疫印迹分析中,MAbCPV40-1与小球藻卵囊提取物中的40 kDa蛋白结合。通过用MAbCPV40-1进行免疫荧光(IFA)染色,将该40 kDa蛋白定位在子孢子细胞质中。在斑点印迹分析中,MAbCPV40-1能够检测10(2)个未经漂白剂处理的和10(2)-10(3)漂白剂处理的小球藻卵囊。 MAbCPV40-1能够检测可溶性和全部小球藻卵囊蛋白提取物中的CPV40抗原,表明在环境样品中检测这种寄生虫的潜在用途。

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