Recombinant Human UAF1/WDR48 His-tag Protein, CF Summary
Details of Functionality
Reaction conditions will need to be optimized for each specific application. We recommend an initial Recombinant Human UAF1 concentration equal to the concentration of deconjugating enzyme present (1:1 stoichiometry) in in vitro deconjugation reactions utilizing Ubiquitin-AMC.
Source
Spodoptera frugiperda, Sf 21 (baculovirus)-derived human UAF1 protein Met1 - Thr677 with a C-terminal 6-His tag
>90%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain
Applications/Dilutions
Dilutions
Bioactivity
Theoretical MW
77 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Publications
Read Publications using E-566 in the following applications:
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
6 months from date of receipt, -70 degreesC as supplied. 3 months, -70 degreesC under sterile conditions after opening.
Buffer
Supplied as a 0.2 μm filtered solution in HEPES, NaCl, TCEP and Glycerol.
Purity
>90%, by SDS-PAGE under reducing conditions and visualized by Colloidal Coomassie® Blue stain
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human UAF1/WDR48 His-tag Protein, CF
KIAA1449DKFZp686G1794
P80
UAF1
USP1 associated factor 1
USP1-associated factor 1
WD repeat domain 48
WD repeat endosomal protein
WD repeat-containing protein 48
WDR48
Background
UAF1 (USP1-Associated Factor 1, also known as WD Repeat-containing protein 48 or WDR48) is a positive regulator of at least three deubiquitinating enzymes of the C19 peptidase family including USP1, USP12, and USP46. In the absence of UAF1, all three of these deubiquitinases are almost completely inactive, and available biochemical evidence suggests UAF1 activation occurs by increasing catalytic turnover as opposed to altered substrate affinity (at least in the case of UAF1/USP1) of the enzymes. Most notably, UAF1 strongly activates USP1 deubiquitination of monoubiquitinated FANCD2 and PCNA, thereby playing important roles in DNA damage response and translesion synthesis. The UAF1/USP12 complex has recently been described as a negative regulator of Notch signaling. Disruption of UAF1-dependent USP12 activity interrupts Notch trafficking to the lysosomes, leading to an increased amount of receptor at the cell surface and to higher Notch activity. At the biochemical level, UAF1/USP12 deubiquitinates the non-activated form of Notch in cell culture and in vitro.
Cohn, M.A., et al. (2009) J. Biol. Chem. 284:5343.
Huang, T.T., et al. (2006) Nat. Cell Biol. 8:339.
Joo, H-Y., et al. (2011) J. Biol. Chem. 286:7190.
Moretti, J., et al. (2012) J. Biol. Chem. 287:29429.
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