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SouthBayBio
K11-linked Tetra-Ubiquitin (human) (rec.) (untagged)
Product Details | |
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Synonyms | Ub4 |
Product Type | Protein |
Properties | |
Source/Host | E. coli |
Sequence |
Four enzymatically conjugated human ubiquitin (aa1-76) (Accession Nr. P0CG47) covalently linked through an isopeptide bond at K11 residue of one ubiquitin molecule and the C-terminal glycine residue of another ubiquitin molecule and untagged. |
Crossreactivity | Human |
MW | ~34kDa |
Purity | ≥95% (SDS-PAGE) |
Concentration | Lot dependent. |
Accession Number | P0CG47 |
Formulation | Liquid. In 50mM HEPES pH 7.5. |
Other Product Data |
Click here for a Typical Lot-specific Product Datasheet from the Original Manufacturer Note: Heating this product in SDS-PAGE buffer can lead to high apparent molecular weight banding or smearing on SDS-PAGE gels that is not representative of the products purity. |
Declaration | Manufactured by South Bay Bio. |
Shipping and Handling | |
Shipping | DRY ICE |
Short Term Storage | -80°C |
Long Term Storage | -80°C |
Handling Advice | Aliquot to avoid freeze/thaw cycles. |
Use/Stability | Stable for at least 1 year after receipt when stored at -80°C. |
Documents | |
MSDS | Inquire |
Product Specification Sheet | |
Datasheet | Download PDF |
The array of cellular processes initiated and regulated by ubiquitin has been partially explained by the structural diversity of differently linked ubiquitin chains. In a ubiquitin chain, ubiquitin moieties can be conjugated through one of their lysine residues (K6, K11, K27, K29, K33, K48 and K63) or the N-terminal methionine residue (M1), offering countless possibilities to assemble a specific polymer. Ubiquitin molecules can also be modified by other post-translational modifications, including acetylation and phosphorylation, adding another layer of ubiquitin signal regulation and diversification. The abundance of K11 linkages strongly increase when the metazoan anaphase-promoting complex APC/C is active during mitosis, and APC/C has been shown to assemble K11-linked ubiquitin chains to drive proteasomal degradation and exit from mitosis.
This protein is formed with wild-type human recombinant ubiquitin and linkage-specific enzymes. Ideal for investigating ubiquitin-binding proteins and as substrates for ubiquitin-specific isopeptidases. Reaction conditions will need to be optimized for each specific application.