张志华. 杨树花叶病毒的酶联免疫吸附分析[J]. 西南林业大学学报, 1984, 4(1): 126-133. DOI: 10.11929/j.issn.2095-1914.1984.01.012
引用本文: 张志华. 杨树花叶病毒的酶联免疫吸附分析[J]. 西南林业大学学报, 1984, 4(1): 126-133. DOI: 10.11929/j.issn.2095-1914.1984.01.012
ENZYME-LINKED IMMUNO-SORBENT ASSAY(ELISA) APPLIED IN POPLAR MOSAIC VIRUS DETECTION[J]. Journal of Southwest Forestry University, 1984, 4(1): 126-133. DOI: 10.11929/j.issn.2095-1914.1984.01.012
Citation: ENZYME-LINKED IMMUNO-SORBENT ASSAY(ELISA) APPLIED IN POPLAR MOSAIC VIRUS DETECTION[J]. Journal of Southwest Forestry University, 1984, 4(1): 126-133. DOI: 10.11929/j.issn.2095-1914.1984.01.012

杨树花叶病毒的酶联免疫吸附分析

ENZYME-LINKED IMMUNO-SORBENT ASSAY(ELISA) APPLIED IN POPLAR MOSAIC VIRUS DETECTION

  • 摘要: 用酶联免疫吸附分析(EUSA)双抗体夹心法,研究杨树花叶病毒(PMV)的定量测定。用纯化的PMV免疫家兔,抗血淸效价经环沉测定为1:1280。

     

    Abstract: This paper described of enzyme-linked immuno-sorbent assay in detecting the poplar mosaic virus.Enzyme was used horseradish peroxidase.Enzyme conjugate was prepaped by pentamethylene aldehyde double method,ELISA was carried out in anti-PMV IgG coated polystyrenemicrotitre plates,purified PMV was used to immunize rabbits for the preparation of antiserum,from which anti-PMV Igc was purified by ammonium sulfate precipitation and then DEAE-cellulose(DE-32) chromatography.In this experiment,the optimun concentration for IgG coating is 5ug/ml and optimum concentration of enzymes conjugate is 4ug/ml.The results indicated that the sensitivity of ELISA to detect purified PMV is 25ng/ml and 1:2430 dilution of diseased leaf sap.

     

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