Affinity Tag Purification
Epitope tagging is a technique that employs genetic engineering to fuse a known epitope, called an affinity tag, to either the C or N terminus of a recombinant protein to facilitate affinity purification and detection. This approach enables high selective capture and circumvents the multistep purification processes that limit throughput during R&D.
The ideal affinity tag should be small in size and as inert as possible to limit any potential interaction with the recombinant protein or proteins that might be present in culture media.
|CaptureSelect™ Novel Affinity Tag System
CaptureSelect™ Affinity Resin is a novel affinity tag system offering the unique selectivity for a small 4 amino acid peptide tag: E-P-E-A (glutamic acid - proline - glutamic acid - alanine), which enables simple purification of C-tagged proteins.
CaptureSelect™ C-tag Resin
Figure 1. GFP-EPEA purification with >90% recovery. Samples from E. coli-derived feed stocks were applied batch-wise to spin columns (400 µL crude sample with 100 µL CaptureSelect™ C-tag Affinity Matrix). Elution: 20 mM Tris, 2 M MgCl2, pH 7. Regeneration/strip: 0.1 M glycine, pH 2.
This shows a green fluorescent protein (GFP) containing a GYQDY-EPEA C-terminal tag purified using CaptureSelect™ C-tag affinity matrix from an E. coli cytoplasmatic fraction. Protein gel analysis of the elution clearly illustrates the recovery of the GFP, as indicated by the green fluorescent signal present in the elution fraction.
Download the Affinity tag application note
Anti-C-tag affinity ligand
In addition to the CaptureSelect™ C-tag affinity resin, the anti-C-tag affinity ligand is also available as conjugated ligand (conjugated to Biotin). This facilitates easy detection and or quantitation of EPEA C-tagged proteins using techniques such as ELISA, Western blot, and label-free platforms (Biacore® and Octet®).
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Researchers at the Institut Curie, Paris, France have used CaptureSelect™ C-tag Affinity Matrix in their research.