- Home
- About
- Products
- E1 Activating
- E2 Conjugating
- E3 Ligase
- Deconjugating
- Proteasome
- Ubiquitin
- All
- Ubiquitin and Ubiquitin Derivatives
- Ubiquitin Chains
- DUB-Resistant, Non-Hydrolyzable Chains
- NH Isopeptide-linked chains
- DCA Linked Chains
- K6-linked Chains (DCA)
- Agarose Bound K6-linked Chains (DCA)
- K11-linked Chains (DCA)
- Agarose Bound K11-linked Chains (DCA)
- K29-linked Chains (DCA)
- Agarose Bound K29-linked Chains (DCA)
- K33-linked Chains (DCA)
- Agarose Bound K33-linked Chains (DCA)
- K48-linked Chains (DCA)
- Agarose Bound K48-linked Chains (DCA)
- K63-linked Chains (DCA)
- Agarose Bound K63-linked Chains (DCA)
- K76-linked Chains (DCA)
- Agarose Bound K76-linked Chains (DCA)
- Ubiquitin Mutants
- Labeled Ubiquitin Proteins
- Antibodies, ELISAs and Kits
- SUMO
- NEDD8
- ISG15
- UFM1
- URM1
- Autophagy
- FAT10
- Inhibitors
- Antibodies
- Kits
- Buffers, Solutions, Standards
- Substrate Proteins
- Affinity Matrices / Proteins
- Fractions
- FUBI
- References
- Orders
- Contact
Material Data Sheet
His6-SENP1 Catalytic Domain
Price: $100.00
His6-SENP1 Catalytic Domain
Price:
100
Quantity:
50 µg
Data Sheet:
Also known as: SUMO specific protease 1 catalytic domain
The covalent modification of proteins by SUMO is reversible and is mediated by SENP enzymes. SENPs cleave residues from the C-terminus of SUMO precursor proteins to generate the mature and active form which contains the conserved C-terminal di-glycine. These enzymes also reverse the process of SUMOylation by removing poly-SUMO conjugates from substrate proteins. SENP1 is active against SUMO-1, SUMO-2 and SUMO-3 in vitro but not ubiquitin or NEDD8. N-terminally tagged SENP1 contains the catalytic domain consisting of residues 415-643. Accession # NP_055369.
Product Information
Stock:
X mg/ml (X mM) in 50 mM Hepes pH 8.0, 100 mM NaCl, 10% glycerol, 5 mM DTT. Concentration will vary with specific Lot #.
MW:
29.8 kDa
Purity:
> 95% by SDS-PAGE Use & Storage
Use:
Typical enzyme concentration to support hydrolysis of substrates in vitro is 50- 500 nM depending on conditions. Pre-incubation (15 min) with 10 mM DTT is recommended to achieve maximum activity.
Storage:
Store at -80°C. Avoid multiple freeze/thaw cycles.
Literature
References:
Bailey D and O’Hare P. (2004) J.Biol.Chem. 279: 692-703
Chen J., et al. (2004) Mol. Cell. Biol. 24:6021-6028
Chen J., et al. (2005) J.Biol.Chem. 280: 14492-14498
Gong L. and Yeh. E.T.H. (1999) J.Biol.Chem. 274:212036-12042
Kim Y.H., et al. (2005) FEBS Lett. 579: 6272-6278
Xu K., et al. (2005) Biochem. J. 386: 325-330
Yamaguchi T., et al. (2005) Mol. Cell. Biol. 12:5171-5182






