Questions about a product, technology or experimental design? Give us a call 610-644-8845
Questions about a product, technology or experimental design? Give us a call 610-644-8845.

NC0105: Non-Cleavable Linear Penta-Ubiquitin

SKU NC-0105-0100 Categories ,
LifeSensors NC0105 is a non-cleavable linear penta-ubiquitin protein, His-tagged, sourced from E. coli, with a molecular weight of 43,033 Da, available in 100µg quantity

$1,167.00

In stock

In stock

**This chain is not recognized by LUB-9, the linear chain-specific monoclonal antibody, nor is it cleaved by Otulin (aka Gumby), the linear chain-specific DUB.** A wide range of cellular processes are modulated through the generation and attachment of polyubiquitin (polyUb) chains to target proteins.  Increasing evidence suggests that polyUb chains joined through linear peptide bonds between the C-terminus of one ubiquitin and the N-terminus of another play important functional roles. The enzyme machinery responsible for the generation of linear polyUb chains has been termed LUBAC, consisting of HOIL-1L and HOIP. Chains of these type have an open conformation, similar to polyUb K63, but with very distinct functional properties. Linear polyUb chains are cleaved by the deubiquitylases CYLD, USP5 (IsoT), USP2 and have been shown to bind to many UBDs including NEMO and Trabin-n (3xnzf). Recombinant penta-ubiquitin is expressed as a linear chain. Amide linkages join the N- and C-terminus of each ubiquitin molecule to each other. This molecule is His-tagged at the N-terminus of the most distal ubiquitin. The methionine residue normally found between each ubiquitin moiety in the chain has been deleted, making this chain resistant to cleavage by otulin as well as not recognized by LUB9, a linear chain specific antibody (Cat. # AB130).

Info

Species Human
Source E. coli
Tag His
Molecular Weight 43,033 Da
Quantity 100µg
Concentration Variable
Formulation  20 mM Tris pH 7.5, 150 mM NaCl, 1 mM EDTA
Storage -80°C, avoid freeze/thaw cycles
 
  • Investigation of binding interactions through pull-down studies
  • Determining potential deubiquitylase activity towards linear chains

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