Simplify Solubilization and Purification of Membrane Proteins

16 Nov 2010
Sarah Sarah
Marketing / Sales

Product news

GE Healthcare’s Membrane Protein Purification Kit is designed for rapid and easy detergent screening of histidine-tagged membrane proteins, enabling simultaneous evaluation of solubilization and purification efficiency. Analysis and evaluation can be performed by a number of methods such as Western blot, gel filtration, or light scattering.

The Kit contains seven detergents in ready-to-use solution (purity ≥ 99% by HPLC analysis), His Mag Sepharose™ Ni, buffer stock solutions, and an easy-to-follow protocol, and is sufficient for two complete screening experiments.

Integral membrane proteins play major roles in fundamental biological processes, and are common targets in the development of pharmaceuticals. To be studied, these proteins must be dispersed in an aqueous solution. To avoid protein loss and deactivation during solubilization and concomitant purification of integral membrane proteins, the choice of detergent is a key factor. Therefore a detergent screen is often necessary to determine the optimal detergent for each protein and purpose.

His Mag Sepharose Ni are magnetic beads designed for rapid, small-scale purification and screening of histidine-tagged proteins from different sources. The high density beads allow rapid capture by magnetic devices, while the visibility of the beads permits reliable collection of the bound histidine-tagged membrane proteins in the screening and purification procedure. Purification of target membrane proteins for a number of analytical or other downstream applications can be achieved within a few hours.

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Western BlottingWestern blotting equipment is used to transfer and identify specific proteins within a sample, reveal protein modifications, as well as give a semi-quantitative estimation of their concentration. Western blotting equipment includes all apparatus necessary to transfer proteins from gel to membrane and subsequent processing steps. Protein transfer can be performed by electroblotting with wet, semi-dry and dry transfer systems onto nitrocellulose and PVDF membranes. Blocking, washing and labeling of membranes follows, involving buffers, blocking reagents, blotting / incubation trays, labeling reagents, immunoblotting assays, antibodies and conjugates. Automated equipment for these steps is available to accelerate your lab workflow. Finally, detection and imaging of proteins can be conducted using gel documentation and imaging systems. Find the best western blotting equipment in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.ProteomicsProteomics is the systemic bioinformatics study of proteins and amino acids, including their structure, size, function and identification. Tools used in proteomics include chromatography, blotting and gels, protein arrays, mass spectrometry and ELISA and associated analysis software. Analyzers and proteomic systems should be sensitive, high resolution, fast and may be automated for high-throughput.Protein PurificationProtein purification is a vital step in drug discovery, therapeutics, biotech and life science research. The purification process typically involves subcellular or membrane protein extraction with cell lysis kits, separation of proteins from cell debris by filtration or spin columns, and the isolation of proteins of interest from other proteins and impurities with affinity purification (including fusion protein tags and antibody binding proteins A, G and L), immunoprecipitation or chromatographic methods, such as ion exchange, size exclusion and immobilized metal affinity chromatography. All purification methods come in multiple formats for your laboratory needs, including agarose or magnetic beads, resins, columns and filter plates. Find the best protein purification equipment in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.
Simplify Solubilization and Purification of Membrane Proteins