CompetitiveRTPCRStrategyforQuantitativeEvaluation4

We have also been able to detect expression of this receptor in all studied tissues, which is consistent with the pleiotropic nature of growth hormone in fish (20–23). The expression level of tiGHR that we obtained for each studied tissue can be organized in decreased order of expression levels as: liver > muscle > brain > heart > gonads > intestine > stomach > spleen (Fig. 6). The highest e......阅读全文

Competitive-RTPCR-Strategy-for-Quantitative-Evaluation-5

3. Characterization of the method precision and repeatability.a. Ensemble PCRs in the same conditions established before using quantities of target in

Competitive-RTPCR-Strategy-for-Quantitative-Evaluation-3

Competitive RT-PCR in Different Tilapia TissuesAbundance levels of tiGHR I mRNA (target) in different tilapia tissues were measured using the quantita

Competitive-RTPCR-Strategy-for-Quantitative-Evaluation-1

Competitive RT-PCR Strategy for Quantitative Evaluation of the Expression of Tilapia (Oreochromis niloticus) Growth Hormone Receptor Type IQuantizatio

Competitive-RTPCR-Strategy-for-Quantitative-Evaluation-2

Determination of Accuracy of the Competitive PCRTo test the precision of the results obtained with this competitive PCR, five different amounts of T (

Competitive-RTPCR-Strategy-for-Quantitative-Evaluation-4

We have also been able to detect expression of this receptor in all studied tissues, which is consistent with the pleiotropic nature of growth hormone

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Protocol-for-competitive-RTPCR

For quantifying mRNA, we use a competitive RT-PCR protocol with internal standard RNAs. These are added in a defined quantity to the RNA sample prior

定量RTPCR-(Quantitative-RTPCR)

Application: Quantitative RT-PCR is used to quantify mRNA in both relative and absolute terms. It can be applied for the quantification of mRNA expres

半定量RTPCR-(SemiQuantitative-RTPCR-)

RT-PCR AnalysisSolutions10X RT Buffer10X PCR Buffer100 mM Tris pH 9.0500 mM KCl1% Triton X-10025 mM MgCl2use at a concentration of 1.5 mMLysis Solutio

反向PCR

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Competitive-ELISA

DAY 11. Coat Nunc immuno-module plates overnight, in usual manner.2. Set up competition assay between antibody and competing substance :-Prepare a 1:2

Quantitative-PCR

实验概要Quantitative PCR involves co-amplification of two templates: a constant amount of a preparation containing the desired target sequence and var

SemiQuantitative-RTPCR

The RT-PCR method can be used not only to detect specific mRNAs but also to semi-quantitate their levels. Thus, one can compare levels of transcripts

SYBR-Green-Quantitative-PCR-Protocol

SummaryQuantitative PCR is a method used to detect relative or absolute gene expression level. All qPCR involves the use of fluorescence to detect the

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ASTRACTWe describe a rapid and quantitative flow cytometric method for determining the apoptotic or anti-apoptotic potential of a gene in various cell

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Purpose...Concentration of proteins in a crude preparations (such as culture sup) can be estimated semi-quantitatively by using "Dot Blot" method if y

PCR

PCRPolymerase Chain Reaction1) Add the following to a microfuge tube:10 ul reaction buffer1 ul 15 uM forward primer1 ul 15 uM reverse primer1 ul templ

A-rapid,-quantitative-and-inexpensive-method-for-detecting-apoptosis2

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mRNA表达的研究 微小残留病变的检测 肿瘤耐药基因表达的研究 病毒感染的定量监测Vs普通PCR,RT-PCR的优势 采用封闭的检测模式,因此扩增产物导致污染的可能性比普通PCR要小得多 。 扩增产物的检测在PCR扩增过程中同时进行,并且数据的采集、分析全部由 仪器 自动完成,因此整个检测所 需的时

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聚合酶链反应(polymerase chain reaction, PCR)是微量核酸扩增的有效工具,由于其灵敏、特异、快速等优点,在医学上已广泛应用与病毒、细菌病原体及遗传病、肿瘤的早期诊断。随着PCR技术的发展,特别是病毒或肿瘤的治疗监测、疾病的诊断、机体基因表达调控方面,不仅需要检测其存在

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RT-PCR or reverse transcription PCR refers to PCR that uses product of an RT reaction as template. In effect, the PCR amplifies cDNA fragments. In one

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RTPCR-PROTOCOL

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RTPCR步骤

总RNA提取1. 取200mg组织,放到1.5ml EP管中,加入1ml Trizol剪碎。2. 震荡30s。3. 加0.2ml氯仿,剧烈摇动30s,室温3min。4. 12000×g,4℃ 离心,15min。5. 吸上层无色水相,移入另一EP管中(约0.5ml)。6. 加等体积异丙醇,-20℃,3

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RT-PCR简介RT-PCR是将RNA的反转录(RT)和cDNA的聚合酶链式扩增(PCR)相结合的技术。首先经反转录酶的作用从RNA合成 cDNA,再以cDNA为模板,扩增合成目的片段。RT-PCR技术灵敏而且用途广泛,可用于检测细胞中基因表达水平,细胞中RNA病毒的含量和直接克隆特定基因的cD

分光光度计的使用

With the aid of spectroscopy, the quantitative analysis of nucleic acids and proteins has established itself as a routine method in many laboratories.