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快速内切酶和修饰酶

快速内切酶和修饰酶

DNA 分子量标准

DNA 分子量标准

蛋白提取、纯化及检测

蛋白提取、纯化及检测

ELISA

ELISA

细胞残留检测

细胞残留检测

TransScript® Uni All-in-One First-Strand cDNA Synthesis SuperMix for qPCR (One-Step gDNA Removal)

目录号: AU341-02

单 价:¥5550

规格:
100 rxns
数量:
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+
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产品详情介绍

TransScript® Uni All-in-One First-Strand cDNA Synthesis SuperMix for qPCR (One-Step gDNA Removal)包含反转录反应所需的全部成分(TransScript® Uni RT, RNase Inhibitor, Anchored Oligo(dT)20 Primer, Random Primer(N9), dNTPs, Buffer),可在同一管反应中实现cDNA 合成和去除基因组DNA。反应时,只需加入5×All-in-One Reaction Mix for qPCR、TransScript® Uni All-in-One Enzyme Mix、模板RNA和水,在42℃-65℃条件下即可高效地合成第一链cDNA,同时去除RNA模板中残留的基因组DNA 。另配有20×No RT Control Mix,用于配制无反转录酶的对照,判断qPCR模板是否来自cDNA。该产品操作简便,降低操作过程中的污染机率。cDNA产物只适用于qPCR,不适用于常规PCR。

产品组成

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References

1 Qin T, Zhang G, Zheng Y, et al. A population of stem cells with strong regenerative potential discovered in deer antlers[J]. Science, 2023.(IF 63.71)

2 Yang L, Wu X, Liu S, et al. Comprehensive Analysis of BrHMPs Reveals Potential Roles in Abiotic Stress Tolerance and Pollen–Stigma Interaction in Brassica rapa[J]. Cells, 2023.(IF 7.66)

3 Yang X, Liu S, Lu W, et al. Delta and jagged are candidate target genes of RNAi biopesticides for the control of Nilaparvata lugens[J]. Frontiers in Bioengineering and Biotechnology, 2022.(IF 6.064)

4 Yuan Y, Fu D, Xu Y, et al. Pt (IV) Prodrug as a Potential Antitumor Agent with APE1 Inhibitory Activity[J]. Journal of Medicinal Chemistry, 2022.(IF 8.039)


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