WELQut Protease | ول کیوت پروتئاز
WELQut Protease | ول کیوت پروتئاز
Cat. No:
FPLF016.0250
FPLF016.0500
FPLF016.1000
Features
- Cleaves outside WELQ recognition sequence, without leaving additional amino acids bound to the target protein.
- Highly specific to cognate recognition site, does not generate non-specific product bands, even after long incubation and using excess of protease.
- Easy to remove from the reaction mixture using built in His-tag.
- Ideal for on-column proteolysis reactions.
Applications
Removal of N-terminal fusion tags from recombinant protein preparations.
19,000,000 ریال
توضیحات محصول
WELQut Protease | ول کیوت پروتئاز
WELQut Protease (5 U/µL)
Cat. No:
FPLF016.0250
FPLF016.0500
FPLF016.1000
Contents:
Kit storage:
This kit should be stored at: -20°C short term (4 months), -80°C long term (more than 1 year).
If properly stored, all kit components are stable until the expiration date printed on the label.
WElQut Protease Storage Buffer:
WElQut Protease contains 10 mM Na2HPO4, 2.7 mM KCl, 1.8 mM KH2PO4, pH 7.3, 140 mM NaCl and, 50% glycerol.
Description
WELQut Protease is highly specific,recombinant serine protease of Staphylococcus aureus. It recognizes and precisely cleaves recombinant proteins containing an engineered recognition sequence* W- E- L- Q-X (Trp, Glu, Leu,Gln, X can be any amino acid). The protease cleaves outside the recognition sequence without leaving additional amino acids bound to the target protein.The WELQut Protease is active in a broad temperature (4-30°C) and pH (pH 6.5-9.0) range and does not require specific buffers. In addition, this new protease has several procedural advantages – it is ideal for on-column proteolysis reactions and can be easily removed from reaction mixtures using its built-in His-tag.
Features
- Cleaves outside WELQ recognition sequence, without leaving additional amino acids bound to the target protein.
- Highly specific to cognate recognition site, does not generate non-specific product bands, even after long incubation and using excess of protease.
- Easy to remove from the reaction mixture using built in His-tag.
- Ideal for on-column proteolysis reactions.
Applications
Removal of N-terminal fusion tags from recombinant protein preparations.
Definition of Activity Unit
Each unit is defined as the amount of enzyme required to cleave ≥ 99% of 100 μg of a control protein in 16 h at 20°C. Enzyme activity is assayed in 100 μl 100 mM Tris-HCl (pH 8.0).
Molecular Weight
22 kDa monomer.
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