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Recombinant Human Ubiquitin Mutant S65A Protein, CF 100 UG

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Recombinant Human Ubiquitin Mutant S65A Protein, CF 100 UG信息二維碼

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Recombinant P. falciparum Ubiquitin Protein, CF  5 MG NEDD8 Conjugation Reaction Buffer Kit  1 KT SUMO Conjugation Reaction Buffer Kit  1 KT Ubiquitin Conjugation Reaction Buffer Kit  1 KT VER 155008  100 UG Radicicol  100 UG

產品介紹

    基本參數

    詳細說明

    • Purity

      >98%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie? Blue stain

    • Activity

      Recombinant Ubiquitin Mutant S65A may be used as a negative control in experiments examining PINK1 kinase activity.  Ubiquitin S65A is not phosphorylated by PINK1 in vitro. Reaction conditions will need to be optimized for each specific application.

    • Source

      E. coli-derived Contains a Ser-to-Ala substitution at position 65.

    • Accession #

    • Predicted Molecular Mass

      8.6 kDa

    UM-S65A

     

    Formulation Lyophilized from a solution in deionized water.


    Reconstitution Reconstitute at 2 mg/ml in an aqueous solution



    Shipping The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.


    Stability & 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.


    Background: Ubiquitin

    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.  Recombinant Ubiquitin Mutant S65A may be used as a negative control in experiments examining the in vitro phosphorylation of Ubiquitin using PINK1 kinase from Red Flour Beetle (Tribolium castaneum) or other sources. Ubiquitin mutant S65A is not phosphorylated by PINK1 in vitro, even in extended reactions.

    • References:

      1. Fiesel F.C., et al. (2015) EMBO Reps. DOI 10.15252/embr.201540514

      2. Kane L.A., et al. (2014) J. Cell Biol. 205: 143

      3. Matsuda N., et al. (2010) J. Cell Biol. 189: 211

      4. Ordureau A., et al. (2014) Mol Cell. 56: 360

      5. Vives-Bauza C., et al. (2010) Proc. Natl. Acad. Sci. 107: 378

      6. Wauer T., et al. (2015) EMBO J. 34: 307

    • Entrez Gene IDs:

      7314 (Human); 298693 (Rat)

    • Alternate Names:

      RPS27A; UBA52; UBB ubiquitin B; UBB; UBC; Ubiquitin











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