Building on decades of established electrophoresis expertise, techniques like isoelectric focusing, SDS-PAGE, and 2D gel electrophoresis remain powerful tools for protein and nucleic acid analysis. SERVA Electrophoresis GmbH, our partner, has revolutionized flatbed electrophoresis with the HPE™ BlueHorizon™. This system delivers unmatched reproducibility and high-resolution separations, offering various configurations to meet your specific needs. Looking to upgrade or replace older instruments like the Multiphor? The HPE™ BlueHorizon™ is the ideal solution. Explore our comprehensive portfolio of ampholytes, buffers, reagents, markers, and electrophoresis gels (agarose, acrylamide, and precast gels) to complete your workflow.
Horizontal flatbed electrophoresis (HPE), particularly the HPE™ BlueHorizon™, offers several advantages over other electrophoresis techniques. Its versatility allows use with:
Isoelectric Focusing (IEF) is valuable technique with a wide range of applications in protein analysis. The ability to separate proteins with high resolution based on their pI makes it an indispensable tool for researchers in many fields. This high resolution even allows for the separation of protein isoforms, which are variants of the same protein that differ in their post-translational modifications (e.g., phosphorylation, glycosylation)
SDS-PAGE (Sodium Dodecyl Sulfate-Polyacrylamide Gel Electrophoresis) is a powerful technique used to separate proteins based on their molecular weight.
2D-PAGE represents the combination of both technologies, Isoelectric Focusing (IEF) and SDS-PAGE. In this technique, proteins are first separated by IEF based on their pI, and then further separated by SDS-PAGE based on their molecular weight. 2D-PAGE provides a highly complex and informative separation of proteins, allowing for the identification and analysis of thousands of proteins in a single sample. It can also be used as preparative techniques for protein purification enabling the isolation of individual proteins or protein fractions from complex mixtures. These purified proteins can then be further analyzed using other techniques such as mass spectrometry or N-terminal sequencing to determine their identity, structure, and function.
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