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首页> 外文期刊>Journal of Neuroscience Methods >Quantitative RT-PCR assay of 5-HT(1A) and 5-HT(2A) serotonin receptor mRNAs using genomic DNA as an external standard.
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Quantitative RT-PCR assay of 5-HT(1A) and 5-HT(2A) serotonin receptor mRNAs using genomic DNA as an external standard.

机译:使用基因组DNA作为外标,对5-HT(1A)和5-HT(2A)血清素受体mRNA进行定量RT-PCR分析。

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摘要

Brain serotonin 5-HT(1A) and 5-HT(2A) receptors have been implicated in both normal and pathological behavior, and in the action of anxiolytic and antidepressant drugs. In this study, detailed description and verification of a new RT-PCR technique to quantify the number of copies of 5-HT(1A) and 5-HT(2A) receptor mRNAs in the brain is presented. The number of copies of beta-actin and 5-HT(1A) or 5-HT(2A) receptor mRNAs in rat brain samples was evaluated with respect to the genomic DNA solution as the external exogenous standard. The expression of 5-HT receptors was calculated as the number of receptor mRNA copies per 100 copies of corresponding beta-actin mRNA. This presented technique is reliable, simple and can be easily set up in any neurobiological laboratory.
机译:脑5-羟色胺5-HT(1A)和5-HT(2A)受体已经参与正常和病理行为,以及抗焦虑药和抗抑郁药的作用。在这项研究中,详细描述和验证了一种新的RT-PCR技术,以量化大脑中5-HT(1A)和5-HT(2A)受体mRNA的拷贝数。相对于作为外部外源标准的基因组DNA溶液,评估了大鼠脑样本中β-肌动蛋白和5-HT(1A)或5-HT(2A)受体mRNA的拷贝数。将5-HT受体的表达计算为每100拷贝相应的β-肌动蛋白mRNA受体mRNA拷贝的数量。该提出的技术可靠,简单,并且可以在任何神经生物学实验室轻松建立。

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