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首页> 外文期刊>The New Microbiologica >Serotyping of foot-and-mouth disease virus by antigen capture-ELISA using monoclonal antibodies and chicken IgY
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Serotyping of foot-and-mouth disease virus by antigen capture-ELISA using monoclonal antibodies and chicken IgY

机译:使用单克隆抗体和鸡IgY的抗原捕获-ELISA法对口蹄疫病毒进行血清分型

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摘要

Laboratory detection of specific foot-and-mouth disease virus (FMDV) is routinely carried out by ELISA and RT-PCR. Identification and serotyping of FMDV by ELISA requires polyclonal antibodies raised in rabbits and guinea pigs. The polyclonal antibodies have certain disadvantages such as batch to batch variation, inconsistent yields of antibodies and limited quantity of serum obtained from individual animals. This paper describes a method wherein monoclonal antibodies and chicken IgY were used in anantigen capture-ELISA for serotyping of thirty tongue epithelia] samples and sixty tissue culture fluids. The results were compared with the routine antigen detection ELISA. The present study indicated that monoclonal antibodies and chicken IgY can substitute conventional polyclonal antibodies for routine serotyping of FMDV.
机译:通常通过ELISA和RT-PCR对特定的口蹄疫病毒(FMDV)进行实验室检测。通过ELISA鉴定和鉴定FMDV的血清型需要在兔和豚鼠中产生多克隆抗体。多克隆抗体具有某些缺点,例如批次间变化,抗体产量不一致以及从单个动物获得的血清量有限。本文描述了一种方法,其中单克隆抗体和鸡IgY用于抗原捕获-ELISA中以对30个舌头上皮样品和60种组织培养液进行血清分型。将结果与常规抗原检测ELISA进行比较。本研究表明,单克隆抗体和鸡IgY可以替代常规多克隆抗体用于FMDV的常规血清分型。

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