Megaplex™ PreAmp 引物,Human Pool Set v3.0
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Applied Biosystems™

Megaplex™ PreAmp 引物,Human Pool Set v3.0

Green features
Megaplex™ PreAmp 引物适合检测灵敏度非常重要的实验,可大幅提升检测低表达水平 MicroRNA 的能力,以尽可能低的样品量(例如低至 1 ng 总 RNA了解更多信息
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货号数量
444474850 reactions
货号 4444748
价格(CNY)
13,095.00
Each
添加至购物车
数量:
50 reactions
价格(CNY)
13,095.00
Each
添加至购物车
Megaplex™ PreAmp 引物适合检测灵敏度非常重要的实验,可大幅提升检测低表达水平 MicroRNA 的能力,以尽可能低的样品量(例如低至 1 ng 总 RNA 的起始样品量)生成全面的表达谱。Megaplex™ PreAmp 引物 (Human Pool Set v3.0) 的成分与 Megaplex™ RT 引物匹配,可搭配 Megaplex™ RT 引物 (Human Pool Set v3.0) 使用。使用 Megaplex™ RT 引物逆转录后,在使用 TaqMan® Array MicroRNA 卡进行实时荧光定量 PCR 定量前,可组合使用 Megaplex™ PreAmp 引物和 TaqMan® PreAmp 预混液均一地扩增所有 microRNA。
仅供科研使用。不可用于诊断程序。
规格
环保功能绿色可持续包装
反应次数50 次反应
引物PreAmp 引物
产品线Megaplex™
产品类型Preamp 引物
数量50 reactions
种属
足够用于50 次反应
高 GC PCR 扩增效果
PCR 方法qPCR
Unit SizeEach
内容与储存
在-20°C条件下储存

常见问题解答 (FAQ)

Can Ct's greater than a cut-off be considered valid results?

Yes they can. However, it is important to recognize the true linearity and detection limits of your assay: Ct values above the cut-off can indicate non-specific amplification, unless your NTC is a true- no-target control, and you have run a statistically significant number of replicates. Any results with Ct above the recommended cut-off need to be validated with individual assays on plates.

What is a good Ct cut-off for the TaqMan MicroRNA Array Cards and TaqMan Advanced miRNA Array Cards? In other words, beyond what Ct should I not trust the data?

The typical Ct cut-off on TaqMan Array Cards is 32, which is equivalent to Ct 35 on a plate (10 µl reaction). Previous studies show that if you use pre-amplification, a Ct cut-off of 29 or 30 can be used to reduce numbers of false positives (see Technical Note Optimized protocols for human or rodent microRNA profiling with precious samples). To ensure that you have selected a correct cut-off, you should run replicates of the same sample and use Ct cut-off before you see an increase in the Standard Deviation.

Why does the negative control well show amplification when doing microRNA analysis using Megaplex Primer Pools and TaqMan Array Cards?

Most likely the reagents or the cDNA template are contaminated. Please follow established PCR laboratory best practices.

Why do I have poor reproducibility across technical replicates when doing microRNA analysis using Megaplex Primer Pools and TaqMan Array Cards?

Most likely the reagents were not adequately mixed. Ensure that all samples and reagents are mixed well.

When doing microRNA analysis using Megaplex Primer Pools and TaqMan Array Cards, why are the Ct values for the endogenous controls highly variable across the sample set?

Highly variable values for endogenous controls is most likely due to biological variation. We recommend that you use an alternative endogenous control, such as a non-variable miRNA.