TruPAGE™ Precast Gels
TruPAGE™ gels offer improved resolution, tear resistance, and an extended shelf-life over the currently available precast polyacrylamide gels. TruPAGE™ gels are formulated with Triethanolamine (TEA)-Tricine, featuring a neutral pH running environment. TruPAGE™ gel cassettes have a hassle-free design. Extra tall wells to prevent lane-to-lane overflow. No comb to remove, preventing torn or bent wells. Instead,…
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Highly recommended
Genetics
When you take the agaros powder, just find the Sigma Aldrich brand.
Review Date: 25 Mar 2022 | Sigma-Aldrich Supelco
Wonderful product for molecular biology
Easy to use for gel electrophoresis
This product is easy to use and useful for molecular biologists, who are working with genome editing, cloning and transformation.
Review Date: 15 Nov 2021 | Sigma-Aldrich Supelco
Great results. Nice gels.
Analyze proteins in tissue
High quality gels and very affordable. Uses less running buffer for gel running. Gels are compatible to the existing gel running apparatus.
Review Date: 31 Jul 2017 | Sigma-Aldrich Supelco
TruPAGE™ gels offer improved resolution, tear resistance, and an extended shelf-life over the currently available precast polyacrylamide gels. TruPAGE™ gels are formulated with Triethanolamine (TEA)-Tricine, featuring a neutral pH running environment.
TruPAGE™ gel cassettes have a hassle-free design.
- Extra tall wells to prevent lane-to-lane overflow.
- No comb to remove, preventing torn or bent wells. Instead, the cassettes lock well fingers in place.
- No tape to remove
TruPAGE Precast Gels are available in 10 x 10 cm and 10 x 8 cm formats, which makes them compatible with the most popular electrophoresis equipment from most manufacturers such as Sigma-Aldrich, Bio-Rad® , Thermo Fisher® , C.B.S. Scientific, Hoefer® , and others.
TruPAGE LDS Sample Buffer should ALWAYS be used to prepare protein samples for use with TruPAGE precast gels to achieve optimal band resolution and sharpness.
The sample buffer is specifically formulated to complement the TruPAGE running buffer system and to deliver the optimal denaturing conditions without causing sample degradation. Effective protein denaturation occurs at 70 ºC instead of the much higher temperature required with Laemmli buffer.
