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Proteasome 19S Rpt6/S8 subunit polyclonal antibody

 
ENZ-ABS284-0100 100 µl 317.00 USD
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Product Specification

Alternative Name:26S protease regulatory subunit 8, Proteasome 26S subunit ATPase 5, TRIP1, Thyroid hormone receptor-interacting protein 1, p45/SUG
 
Host:Rabbit
 
Isotype:IgG
 
Immunogen:Full-length recombinant human 19S Rpt6/S8 subunit.
 
UniProt ID:P62195
 
Species reactivity:Human
 
Specificity:Recognizes the Rpt6/S8 subunit of the 19S regulator complex.
 
Applications:IP, WB
 
Application Notes:Detects a band of ~45kDa by Western blot.
 
Purity Detail:Ammonium sulfate precipitation
 
Formulation:Liquid. In PBS containing 1mg/ml BSA and 0.05% sodium azide.
 
Handling:Avoid freeze/thaw cycles.
 
Shipping:Shipped on Blue Ice
 
Long Term Storage:-20°C
 
Scientific Background:Proteolytic degradation is critical to the maintenance of appropriate levels of short-lived and regulatory proteins as important and diverse as those involved in cellular metabolism, heat shock and stress response, antigen presentation, modulation of cell surface receptors and ion channels, cell cycle regulation, transcription, and signalling factors. The ubiquitin-proteasome pathway deconstructs most proteins in the eukaryotic cell cytosol and nucleus. Others are degraded via the vacuolar pathway which includes endosomes, lysosomes, and the endoplasmic reticulum.

The 26S proteasome is an ATP-dependent, multisubunit (~31), barrel-shaped molecular machine with an apparent molecular weight of ~2.5 MDa. It consists of a 20S proteolytic core complex which is crowned at one or both ends by 19S regulatory subunit complexes. The 19S regulatory subunits recognize ubiquitinated proteins and play an essential role in unfolding and translocating targets into the lumen of the 20S subunit. An enzymatic cascade is responsible for the attachment of multiple ubiquitin molecules to lysine residues of proteins targeted for degradation. Several genetic diseases are associated with defects in the ubiquitin-proteasome pathway. Some examples of affected proteins include those linked to cystic fibrosis, Angelman’s syndrome, and Liddle syndrome.
 

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