UltraPure™ 甲酰
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Invitrogen™

UltraPure™ 甲酰

UltraPure™ 甲酰胺常用于变性核酸,以进行测序凝胶电泳、电子显微镜分析和杂交。UltraPure™ 甲酰胺在室温下呈液态,经过真空蒸馏,在干燥的氮气下包装,自购买之日起三个月内可用于多种应用。由于甲酰胺分解产物会降解核酸,因此对于敏感应用,应在使用前通过混合床离子交换树脂处理使甲酰胺去离子化了解更多信息
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货号数量
15515026500 g
货号 15515026
价格(CNY)
1,811.00
飞享价
Ends: 31-Dec-2025
2,157.00
共减 346.00 (16%)
Each
添加至购物车
数量:
500 g
价格(CNY)
1,811.00
飞享价
Ends: 31-Dec-2025
2,157.00
共减 346.00 (16%)
Each
添加至购物车
UltraPure™ 甲酰胺常用于变性核酸,以进行测序凝胶电泳、电子显微镜分析和杂交。UltraPure™ 甲酰胺在室温下呈液态,经过真空蒸馏,在干燥的氮气下包装,自购买之日起三个月内可用于多种应用。由于甲酰胺分解产物会降解核酸,因此对于敏感应用,应在使用前通过混合床离子交换树脂处理使甲酰胺去离子化。
仅供科研使用。不可用于诊断程序。
规格
适用于(应用)细胞成像/核酸凝胶电泳和印迹
产品线UltraPure™
产品类型甲酰胺
纯度不含 DNase、不含 RNase
数量500 g
运输条件经批准可在室温下或置于湿冰上运输
形式液体
Unit SizeEach
内容与储存
储存在冰箱 (2–8°C) 中。

常见问题解答 (FAQ)

Can a sample buffer with formamide be used with the Invitrogen TBE-Urea system?

There are many sample buffer formulations used, however we have found a distinct difference in the band appearance depending on the sample buffer composition. After evaluating urea, formamide, and various buffer systems, we found that the sharpest, flattest bands were obtained with a urea, Ficoll, and TBE buffer solution. Sample buffers made with formamide resulted in fuzzy, indistinct bands.

Find additional tips, troubleshooting help, and resources within our Nucleic Acid Purification and Analysis Support Center.

Is formamide (Cat. No. 15515-026) supplied as a liquid? When is deionization required, and can you provide a protocol?

Yes, formamide is supplied as a liquid even though it is sold by weight.

It is appropriate to use out of the bottle for most applications (hybridization buffer, loading buffers for sequencing gels, and formaldehyde-containing RNA gels) if less than one year old and stored properly (-20 degrees C). (If formamide smells like ammonia, it is probably breaking down and should not be used.) However, we have seen that in a protocol we have for running RNA gels without formaldehyde in the gel, freshly deionized formamide is essential for preparation of the loading buffer. That protocol as well as the protocol for deionizing the formamide follows:

These reagents are used in electrophoresis of RNA in agarose gels in 1X MOPS EDTA buffer. (Note: no formaldehyde is used in the gel.) The sample is prepared in the sample buffer (1.5 to 3 µL sample mixed with sample buffer). Heat the RNA in sample buffer for 10 min at 65 degrees C. Place on ice immediately then load gel.

10X MOPS EDTA (10X ME)

(1) Measure out 700 mL DEPC-treated water in a DEPC-treated 1-liter graduated cylinder and place in a DEPC-treated 1-liter beaker.
(2) Place beaker on stir plate and begin stirring with a DEPC-treated stir bar.
(3) Add 104.65 g MOPS to beaker. Weigh out MOPS using a sterile-flamed spatula from an unopened bottle MOPS or one set aside for RNA only. Dissolve by stirring.
(4) Add 40 mL 0.25 M EDTA to solution. Note: the EDTA solution should be made with DEPC-treated processed water.
(5) Adjust pH to 7.0 by adding 10 N NaOH (~20 mL)
(6) Bring up to 1 liter volume with DEPC-treated water.
(7) Filter solution using a 0.2 µm Nalgene filter unit.
(8) Store at 4 degrees C for six months in a DEPC-treated glass bottle. (This prevents solution from yellowing.) NOTE: The presence of yellow color does not affect the performance of the buffer.

Formamide Deionization protocol:
1. Add 1 g mixed bed, ion exchange resin for every 10 ml of formamide. Suitable ion exchange resins include BioRad AG501-X8 and Fisher Resin 1-300.
2. Stir for 30 to 60 min @ RT.
3. Filter through Whatman No. 1 filter paper.
4. Dispense into units of use and store at -20°C