Pour your own polyacrylamide (SDS-PAGE) mini or midi gels with our sealed empty gel cassettes. These cassettes give you the option of hand casting your own gels while enjoying the benefits of the Mini Gel Tank and SureLock systems.
In biolaboratories, agarose gel electrophoresis is the modus operandi for size-based separation of DNA and RNA fragments. The agarose gel matrix is porous and acts as a sieve through which the nucleic acid molecules migrate.
Pour your own polyacrylamide mini gels easily and confidently with the Invitrogen SureCast Gel Handcast System. Request a demo Leak-free* design Durable glass plates Single component assembly using a single-motion load-and-lock mechanism Unique tilt feature- minimizes spillage during gel casting,...
Two-dimensional (2D) gel electrophoresis is a powerful and sensitive technique for separating and analyzing protein mixtures from biological samples. 2D gel electrophoresis is performed in two consecutive steps, IEF and SDS-PAGE.
We offer a wide variety of staining and drying accessories to help you process your protein gel electrophoresis gels., The StainEase® Staining Tray is a convenient way to evenly stain minigels and prevent gels from breaking. Easily fits up to 4 mini- or midi-gels.
DNA electrophoresis is a standard laboratory technique used to identify, quantify, and purify DNA fragments. DNA electrophoresis involves loading DNA samples into the wells of an agarose or acrylamide gel and subjecting it to an electric field.
Finding the right protein gel electrophoresis system is critical to getting consistent and accurate results you need for your research. Electrophoresis buffers and reagents are important components of the protein electrophoresis system.
In the nucleic acid electrophoresis workflow, several steps are performed sequentially, each of which could impact the outcome of nucleic acid separation. This article addresses five considerations associated with samples, reagents, and running parameters.
Gel electrophoresis is a common laboratory technique to isolate nucleic acids and proteins. Nucleic acid electrophoresis uses a gel matrix to separate DNA and RNA fragments based on size and molecular weight. Gel electrophoresis is vital in all molecular biology workflows.
In this article: What is Power Snap Plus System Designed for high-throughput SYBR safe pre-cast gels Discover more, Gel electrophoresis is a laboratory procedure that is foundational to analyze proteins and nucleic acids. Gel electrophoresis is considered a workhorse of molecular biology research.
(See a list of the products featured in this article.) Polyacrylamide gel electrophoresis (PAGE)—an important technique for separating proteins based on their electrophoretic mobility—is widely used for both protein analysis and protein purification.
Perform agarose gel electrophoresis of nucleic acids using tanks, combs, power supplies, and other accessories of Thermo Scientific™ Owl™ Horizontal Gel Electrophoresis Systems. Choose among the following format series: large (A1-A6), micro (C2-S), wide (D2-D4), and mini (EasyCast™ B1-B3).
Explore: Protein electrophoresis products Download: Protein Electrophoresis Handbook, Protein electrophoresis is a standard laboratory technique by which charged protein molecules are transported through a solvent by an electrical field.
Most life science researchers will run a gel at some point in their careers. Running a gel, formally called gel electrophoresis, is an effective method to separate biomolecules, such as nucleic acids and proteins , based on size.
Nucleic acid electrophoresis is a standard laboratorytechnique that underpins molecular biology research. Traditionally, gel electrophoresis takes a lot of time and involves casting the gel, making buffers, preparing samples and ladders, loading and running the gel,as well as visualizing and imaging...