5-(3-氨基烯丙基)-dUTP (50 mM)
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5-(3-氨基烯丙基)-dUTP (50 mM)
Invitrogen™

5-(3-氨基烯丙基)-dUTP (50 mM)

当掺入 DNA 时,5-(3-氨基烯丙基)-dUTP 提供反应性基团,用于添加其他化学基团。改性 dUTP 可通过逆转录酶来掺入。氨基烯丙基改性可实现与胺反应性化合物(如 N-羟基琥珀酰亚胺了解更多信息
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货号数量
AM843950 μL
货号 AM8439
价格(CNY)
2,327.00
飞享价
Ends: 31-Dec-2025
3,392.00
共减 1,065.00 (31%)
Each
添加至购物车
数量:
50 μL
请求批量或定制报价
价格(CNY)
2,327.00
飞享价
Ends: 31-Dec-2025
3,392.00
共减 1,065.00 (31%)
Each
添加至购物车
当掺入 DNA 时,5-(3-氨基烯丙基)-dUTP 提供反应性基团,用于添加其他化学基团。改性 dUTP 可通过逆转录酶来掺入。氨基烯丙基改性可实现与胺反应性化合物(如 N-羟基琥珀酰亚胺 (NHS) 酯)的下游反应;因此氨基烯丙基改性 cDNA 可使用任何胺反应性基团标记。

使用该改性核苷酸:
按照您的逆转录方案中的推荐使用 5-(3-氨基烯丙基)-dUTP。使用 5-(3-氨基烯丙基)-dUTP 替代 30–80% dTTP 可能会有用,但是确切比例将取决于实验目标。
仅供科研使用。不可用于诊断程序。
规格
产品线Ambion™
产品类型核苷酸
纯化方法HPLC
数量50 μL
运输条件干冰
最大浓度50 mM
适用于(应用)Nucleic Acid Labeling
形式液体
标签或染料未标记
Unit SizeEach
内容与储存
储存于 -70° C 或更低温度条件下。避免多次冻融循环。产品等份试液可以在 -20° C 条件下短期储存。不要将其储存于无霜冰箱内。

常见问题解答 (FAQ)

Why are there only two amino-modified nucleotides in the dNTP mix for cDNA indirect labeling (aminoallyl-dUTP and aminohexyl-dATP) intead of all four nucleotides being modified? Would more modified nucleotides have an adverse effect on the microarray?

Using four modified nucleotides rather than two can cause fluorescence quenching since the fluorophores are positioned very closely to one another. Use of two amino-modified nucleotides in the cDNA synthesis reaction (rather than one) results in a greater incorporation of fluorescent dye and higher signal intensity with small amounts of RNA starting material. Unbiased incorporation of amino-modified dNTPs and the high efficiency of the coupling reaction result in an even distribution of fluorescent signal and high overall levels of fluorescence, increasing the sensitivity and reproducibility of array hybridizations. In addition to quenching, a very high dye density on the cDNA will interfere with hybridization and, therefore, yield lower microarray fluorescence signals. We found that the use of 2 amino-modified nucleotides (at the appropriate concentration) results in optimal incorporation and high microarray signals.

Can dU-containing DNA produced by amplification with dUTP be cut by restriction enzymes?

You will need to confirm with the manufacturer of the restriction enzyme you are using to find out whether or not it can recognize dUTP-containing DNA.

Find additional tips, troubleshooting help, and resources within our PCR and cDNA Synthesis Support Center.