Novex™ Value™ 4-20%, Tris-甘氨酸, 1.0 mm, 小型蛋白预制胶, 10 孔
Invitrogen™
Novex™ Value™ 4-20%, Tris-甘氨酸, 1.0 mm, 小型蛋白预制胶, 10 孔
Novex™ Value Tris-Glycine Mini Gels provide a great balance of price and performance for your protein separation needs. Novex Value了解更多信息
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货号
数量
XV04200PK20
20 支/包
货号 XV04200PK20
价格(CNY)
2,349.00
20 gels (1 box)
添加至购物车
数量:
20 支/包
价格(CNY)
2,349.00
20 gels (1 box)
添加至购物车
Novex™ Value Tris-Glycine Mini Gels provide a great balance of price and performance for your protein separation needs. Novex Value Tris-Glycine polyacrylamide gels provide good separation and resolution of your proteins in an affordable gel that is based on traditional Laemmli protein electrophoresis. Each box contains 20 gels.
Features of the Novex Value gels include: • Excellent balance of value and performance—great for qualitative analysis (e.g., screening, protein purification verification) • Fast run conditions—separate your proteins using constant voltage in less than 60 minutes • Options for native and denaturing protein assays
Choose the right gel format for your experiments Novex Value Tris-Glycine gels come in a fixed 10% option as well 4–12% and 4–20% gradients.
Run your proteins in native or denatured form Novex Value Tris-Glycine gels do not contain SDS and can be used to run your proteins in native or denatured form. For denatured proteins, we recommend using Novex Tris-Glycine SDS Sample Buffer and Novex Tris-Glycine SDS Running Buffer. For native proteins, we recommend using Novex Tris-Glycine Native Sample Buffer and Novex Tris-Glycine Native Running Buffer.
For transferring your proteins to membrane, we recommend using Novex Tris-Glycine Transfer Buffer. Transfers can be done using the Mini Blot Module or the iBlot™ Gel Transfer Device.
I am transferring a Tris-Glycine gel using constant voltage and the current reading is way over the expected starting current. Can you offer some suggestions?
The most common cause of abnormally high current is the transfer buffer. If the transfer buffer is too concentrated, this leads to increased conductivity and current. High current may also occur if Tris-HCl is accidentally substituted for the Tris base required in the transfer buffer. This will again result in low buffer pH and lead to increased conductivity and current and subsequently, overheating. We recommend checking the transfer buffer and its reagent components and re-diluting or remaking the buffer.