Recombinant Human Phospho-Ubiquitin (S65) Protein, CF

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications Bioactivity
Format
Carrier-Free

Order Details

Recombinant Human Phospho-Ubiquitin (S65) Protein, CF Summary

Modification
p Ser65
Details of Functionality

Reaction conditions will need to be optimized for each specific application.

Source
E. coli-derived human Ubiquitin protein
Met1 - Gly76
Phosphorylated on Ser 65.
Accession #
Protein/Peptide Type
Recombinant Proteins
Gene
UBB
Purity
>98%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain.

Applications/Dilutions

Dilutions
  • Bioactivity
Theoretical MW
8.6 kDa.
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.
Publications
Read Publications using
U-102 in the following applications:

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 6 months from date of receipt, -20 to -70 °C as supplied.
  • 3 months, -20 to -70 °C under sterile conditions after opening.
Buffer
Supplied as a solution in HEPES.
Purity
>98%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain.

Notes

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

Alternate Names for Recombinant Human Phospho-Ubiquitin (S65) Protein, CF

  • RPS27A
  • UBA52
  • UBB ubiquitin B
  • UBB
  • UBC
  • Ubiquitin

Background

Serine/Threonine kinase PINK1 (PTEN-induced putative kinase protein 1) plays a critical role in preventing mitochondrial dysfunction during cellular stress. PINK is translated in the cytosol, then translocated to the outer mitochondrial membrane where it is rapidly cleaved and degraded as a part of normal mitochondrial function. In damaged (depolarized) mitochondria PINK becomes stabilized and accumulates, resulting in the subsequent phosphorylation of numerous proteins on the mitochondrial surface including Mfn2.  Ultimately PARK2 (E3 Ubiquitin Ligase Parkin) is recruited to the damaged mitochondria where it is activated by PINK-mediated phosphorylation of PARK2 at serine 65, and PARK2 interaction with phosphorylated Ubiquitin (also phosphorylated by PINK on serine 65). This signaling cascade is critical for clearing the damaged mitochondria via selective autophagy (mitophagy) by mediating activation and translocation of PARK2.


  1. Matsuda N. et al. (2010) J. Cell Biol. 189: 211.
  2. Kane L.A. et al. (2014) J. Cell Biol. 205:143.
  3. Ordureau A. et al. (2014) Mol Cell. 56: 360.
  4. Vives-Bauza C. et al. (2010) Proc. Natl. Acad. Sci. 107: 378.
  5. Wall C.E. et al. (2019) Cell Reports  29: 3280.
  6. Wauer T. et al. (2015) EMBO J. 34: 307.

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Publications for Ubiquitin (U-102)(2)

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Bioinformatics

Gene Symbol UBB
Uniprot