ATP是某些酶类反应的供能底物。

含相同摩尔数的超纯 dATP、dCTP、dGTP 和 dTTP。每种的浓度为 10 mM。

含有 100 mM dATP，pH 7.4 的钠盐溶液。

含相同摩尔数的超纯 dATP、dCTP、dGTP 和 dTTP。每种的浓度为 10 mM。

含有 5 mM 7-去氮-dGTP 的二锂盐溶液。

四种独立包装的核苷三磷酸溶液（ATP、CTP、GTP 和 UTP），pH 7.5，以钠盐形式存在。

四种独立包装的 acyNTP （acyATP、acyCTP、acyGTP 和 acyTTP）。以干粉形式提供，加入 50 μl 蒸馏水或去离子水（Milli-Q®）后，acyNTP 的终浓度为 10 mM。acyNTP 可作为链终止基团，因而可用于一般采用 ddNTP 的实验，如 DNA 测序和 SNP 分析。acyNTP 尤其适用于古生菌 DNA 聚合酶的反应，特别是 Therminator DNA 聚合酶。Therminator DNA 聚合酶经过基因工程改造后，拥有更强的掺入核苷酸类似物的能力，这些类似物的糖环发生了改变，如 rNTP，ddNTP，2´ 脱氧核苷酸，特别是 acy 碱基类似物。

含相同摩尔数的四种核苷三磷酸：rATP、rCTP、rGTP 和 rUTP。每种浓度为 25 mM（rNTP 总浓度相当于 100 mM）。

10 mM 溶液，pH 7.0。

ATP是某些酶类反应的供能底物。

四种独立包装的超纯脱氧核苷三磷酸的溶液（dATP、dCTP、dGTP 和 dTTP）。每种的浓度为 100 mM。

含相同摩尔数的超纯 dATP、dCTP、dGTP 和 dTTP。每种的浓度为 10 mM。

含有 5 mM 7-去氮-dGTP 的二锂盐溶液。

四种独立包装的核苷三磷酸溶液（ATP、CTP、GTP 和 UTP），pH 7.5，以钠盐形式存在。

含相同摩尔数的四种核苷三磷酸：rATP、rCTP、rGTP 和 rUTP。每种浓度为 25 mM（rNTP 总浓度相当于 100 mM）。

反应中所用到的标记 GTP 3'- 脱硫生物素 - GTP 还能提供一种便捷的标记方法，将 5´ 末端带有三磷酸的任何 RNA 进行标记。

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

Total RNA which has been extracted from cell lines representing different mouse tissues, pooled (11 mouse), and treated to remove DNA to undetectable levels. Typical uses include optimization of primer/probe sets to ensure no cross reactivity, as a standard to relatively quantitate unknowns to an unchanging reference for immediate validation without wasting precious RNA, or to compare QPCR efficiencies across labs/platforms/experiments.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

Total RNA which has been extracted from cell lines representing different human tissues, pooled (10 human), and treated to remove DNA to undetectable levels. Typical uses include optimization of primer/probe sets to ensure no cross reactivity, as a standard to relatively quantitate unknowns to an unchanging reference for immediate validation without wasting precious RNA, or to compare QPCR efficiencies across labs/platforms/experiments.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

The MVP Total RNA was isolated using a modified guanidinium thiocyanate method that has been validated to co-purify both miRNA and mRNA and delivers RNA suitable for QRT-PCR. MVP Total RNA is the ideal choice for many applications,including QRT-PCR,miRNAdetection,Northern blot analysis,cDNA synthesis,RT-PCR,in vivio translation, ribonuclease protection assays, S1 nuclease analysis,and microarray target labeling.

MVP RNA (MVP Mouse BALB/c Male Total RNA) is application-ready RNA available in small economical pack sizes. Extensive and rigorous quality control including many application specific assays provides assurance that the RNA is intact, full-length and nearly DNA-free.

Total RNA, Kidney, C57BL, Mal

Total RNA, Liver, C57BL, Male