Recombinant Human Poly-Ub WT Chains (1-7) (K48-linked), CF

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Summary
Product Discontinued
View other related Poly-Ubiquitin Peptides and Proteins

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    • Catalog Number
      UC-240
    • Availability
      Product Discontinued

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Recombinant Human Poly-Ub WT Chains (1-7) (K48-linked), CF Summary

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

Applications/Dilutions

Dilutions
  • Enzyme Activity
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.

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 12 months from date of receipt, -20 to -70 °C as supplied.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
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.

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human Poly-Ub WT Chains (1-7) (K48-linked), CF

  • CEP80
  • HEL112
  • PolyUbiquitin
  • Poly-Ubiquitin
  • ribosomal protein S27a
  • RPS27A
  • S27A
  • UBA80
  • UBC
  • UBCEP1
  • UBCEP80

Background

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.

  1. Scheffner, M. et al. (1995) Nature 373:81.
  2. Sharp, P.M. & W.-H. Li (1987) Trends Ecol. Evol. 2:328.
  3. Behrends, C. & J.W. Harper (2011) Nat. Struct. Mol. Biol. 18:520.
  4. Greene, W. et al. (2012) PLoS Pathog. 8:e1002703.
  5. Henry, A.G. et al. (2012) Dev. Cell 23:519.
  6. Tong, X. et al. (2012) J. Biol. Chem. 287:25280.
  7. Wei, W. et al. (2004) Nature 428:194.
  8. Zhang, J. et al. (2012) J. Biol. Chem. 287:28646.

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