Recombinant Human His6-PolyUb WT Chains (2-7,K63-linked), CF 100 UG

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Recombinant Human His6-PolyUb WT Chains (2-7,K63-linked), CF 100 UG信息二维码

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产品介绍

    基本参数

    详细说明

    • Purity

      >95%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain.

    • Activity

      Ubiquitin chains vary in length, linkage, and function. K63-linked His6-Poly-Ubiquitin Chains (Ub2-7) 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 Contains a 6-His tag

    • Accession #

    • Predicted Molecular Mass

      19 kDa (Ub2), 29 kDa (Ub3), 38 kDa (Ub4), 48 kDa (Ub5), 57 kDa (Ub6), and 67 kDa (Ub7)

    UCH-330

     

    Formulation X mg/ml in sterile, deionized water





    Shipping The product is shipped with polar packs. 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 opening.


    Background: Poly-Ubiquitin

    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 proteins that contain Ubiquitin-associated domains (UBAs) or ubiquitin-interacting motifs (UIMs). Lys63-linked poly-Ubiquitin has been implicated in several non-degradative processes such as receptor endocytosis and sorting, translation, DNA damage repair, the stress response and signaling in theNF kappa B pathway. This product is formed with wild-type human recombinant Ubiquitin and linkage-specific enzymes. This mixture of poly-Ubiquitin chains contains di-Ubiquitin and higher MW species; mono-Ubiquitin has been removed.


    The His6-tag is convenient for metal chelate affinity purification and immuno-detection using His6-specific antibodies.

    • References:

      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.

    • Alternate Names:

      PolyUbiquitin; Poly-Ubiquitin








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