Tris-甘氨酸转印缓冲液 (25X)
Tris-甘氨酸转印缓冲液 (25X)
Invitrogen™

Tris-甘氨酸转印缓冲液 (25X)

Tris-甘氨酸转印缓冲液 (25X) 针对蛋白至硝酸纤维素膜、PVDF 或尼龙膜的 Western 印迹转印进行了优化,有助后续采用 Tris-甘氨酸凝胶进行分析。使用方法:该缓冲液应用水/甲醇混合物(甲醇终浓度为了解更多信息
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货号数量
LC3675500 mL
货号 LC3675
价格(CNY)
712.00
Each
添加至购物车
数量:
500 mL
价格(CNY)
712.00
Each
添加至购物车
Tris-甘氨酸转印缓冲液 (25X) 针对蛋白至硝酸纤维素膜、PVDF 或尼龙膜的 Western 印迹转印进行了优化,有助后续采用 Tris-甘氨酸凝胶进行分析。

使用方法:该缓冲液应用水/甲醇混合物(甲醇终浓度为 20%)稀释为 1X 溶液,从而获得理想的结果。

查看所有 SDS-PAGE 可用的缓冲液和试剂

仅供科研使用。不可用于诊断程序。
规格
最大浓度25X
凝胶类型Tris-甘氨酸预制胶
数量500 mL
运输条件室温
凝胶兼容性Novex™ Tris-甘氨酸凝胶
膜兼容性硝酸纤维素膜、PVDF、尼龙
产品线Novex™
产品类型转印缓冲液
Unit SizeEach
内容与储存
在室温下储存。

常见问题解答 (FAQ)

我的转膜缓冲液的pH值偏离推荐值0.2单位,能否继续使用?

我们建议丢弃缓冲液,并在再次检查试剂和水的纯度后重新配制。不建议用酸或碱调节pH,因为这会使缓冲液的电导率升高,导致转印期间电流过高。

What type of transfer buffer should be used with Invitrogen Tricine gels?

For non-sequencing applications, any transfer buffer used with Tris-Glycine gels can be used with Tricine gels including Tris-Glycine transfer buffer. For sequencing applications, the buffer should be chemically compatible with sequencing protocols. Non-glycine based transfer buffers such as the NuPAGE Transfer buffer, 1/2X TBE Transfer buffer, or CAPS Buffer can be used for N-terminal sequencing . Generally, a pH which is close to neutral is desirable to maintain gel and protein stability. High current should be avoided because it can lead to heat generation and instability.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

When blotting with the XCell II Blot Module, what would happen if I filled the outer buffer chamber with transfer buffer instead of water?

This is perfectly acceptable with the XCell II Blot Module. The liquid in the outer buffer chamber only serves as a coolant or heat sink. The reason why water is recommended is because it is a less expensive alternative.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

The pH of my transfer buffer deviates from the recommended value by 0.2 units. Can I still use the buffer?

We recommend discarding the buffer and remaking it after rechecking the reagents and the water purity. We do not recommend adjusting the pH with acid or base, as this will increase the conductivity of the buffer and result in higher current during the transfer.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.