犬SLAM受体mRNA荧光定量PCR检测方法的建立和初步应用
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北京市属高等学校人才强教计划资助项目


Development and Application of Fluorescent Quantitative RT-PCR for Detecting SLAM mRNA in Canine
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    摘要:

    【摘要】:目的:建立荧光定量PCR方法,检测犬不同组织中SLAM受体mRNA的表达水平。方法:以犬GAPDH 为内参基因采用△△Ct法,分析SLAM受体mRNA在犬体内不同组织中的表达。结果:此方法有较高的重复性,变异系数在0.89 %- 2.35 % 。以SLAM受体在心脏的表达为1倍值,结果显示受体mRNA在脾脏中表达最高,为38.49倍;肺门淋巴结、肠系膜淋巴结、腹股沟淋巴结中表达次之,分别为9.13、8.58、6.24倍;膀胱中表达最低。结论:成功建立了检测SLAM受体mRNA在不同组织中表达水平的荧光定量PCR检测方法。

    Abstract:

    【Abstract】: Objective: To establish a method for the detection of mRNA transcription of SLAM as CDV receptors in different tissues of canine. Method: By using GAPDH as the house keeper, The △△Ct relative quantification method was used to detect the transcription levels of SLAM mRNAs in different tissues of canine. Result: The inter-assay variability (CV %) were0.89 %- 2.35 %. The results indicated that the qPCR had advantages of high reproducibility. Results of the study showed that the SLAM mRNA were transcripted at high level in the spleen, hilar lymph node, lymphonodi mesosteniales, inguinal glands and low level in the urinary bladder. Conclusion: The quantitative RT-PCR method was established successfully for the detection of mRNA transcription of SLAM in different tissues of canine.

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夏菁,李佳,姜代勋,陈武.犬SLAM受体mRNA荧光定量PCR检测方法的建立和初步应用[J].中国比较医学杂志,2013,23(6).

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  • 收稿日期:2013-04-07
  • 最后修改日期:2013-04-15
  • 录用日期:2013-05-13
  • 在线发布日期: 2013-07-02
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