| Details of Functionality | Ubiquitin chains vary in length, linkage, and function. K48-linked Poly-Ubiquitin Chains (Ub1-7) are ideal for investigating Ubiquitin-binding proteins and as substrates for Ubiquitin-specific isopeptidases. Reaction conditions will need to be optimized for each specific application. IMPORTANT: Heating this product in SDS-PAGE buffer or terminating reactions containing this product with heated SDS-PAGE buffer could lead to unexpected, high apparent molecular weight banding or smearing on gels that is not representative of product purity. For optimal results, we recommend incubation in SDS-PAGE buffer + DTT at <40 °C for 20 minutes prior to gel electrophoresis. |
| Source | E. coli-derived human Poly-Ubiquitin protein P0CG47 |
| Protein/Peptide Type | Recombinant Proteins |
| Purity | >95%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain |
| Dilutions |
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| Theoretical MW | 8.6 kDa (Ub), 17 kDa (Ub2), 26 kDa (Ub3), 34 kDa (Ub4), 43 kDa (Ub5), 52 kDa (Ub6), and 60 kDa (Ub7) .Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
| Storage | Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
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| Buffer | Lyophilized from a solution in deionized water. |
| Purity | >95%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain |
| Reconstitution Instructions | Reconstitute at 5 mg/mL in an aqueous solution. |
Poly-Ubiquitin chains are composed of Ubiquitin monomers that are covalently linked through isopeptide bonds, which typically form between a lysine residue of one Ubiquitin molecule and the C-terminal glycine residue of another Ubiquitin molecule (1). Each human Ubiquitin monomer is 76 amino acids (aa) in length and shares 96% and 100% aa identity with yeast and mouse Ubiquitin, respectively (2). Seven of the 76 aa in Ubiquitin are lysine residues that can participate in poly-Ubiquitin chain formation. Linkage through specific lysine residues is thought to serve as a signal that affects protein degradation, signaling, trafficking, and other cellular processes (3-8).
Linkage specific poly-Ubiquitin chains are used to investigate mechanisms of chain recognition,binding and hydrolysis by the proteasome, deubiquitinating enzymes, E3 ligases or other proteinsthat contain ubiquitin-associated domains (UBAs) or ubiquitin-interacting motifs (UIMs). Lys48-linked chains are abundant in vivo and act as a universal signal for proteasomal degradation. This product is formed with wild-type human recombinant Ubiquitin and linkage-specific enzymes.The poly-Ubiquitin chain mixture contains mono-Ubiquitin and higher MW species up to hepta-Ubiquitin.
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