SUMO Protease, also known as Ulp, is a recombinant fragment of ULP1 (Ubl-specific protease 1) from Saccharomyces cerevisiae. It isRead more
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Catalog number 12588018
Price (USD)
676.00
Each
Add to cart
Price (USD)
676.00
Each
Add to cart
SUMO Protease, also known as Ulp, is a recombinant fragment of ULP1 (Ubl-specific protease 1) from Saccharomyces cerevisiae. It is highly specific for the SUMO protein fusion, recognizing the tertiary structure of SUMO rather than an amino acid sequence. The SUMO Protease features:
• Highly active cleavage • No non-specific proteolysis (highly specific cleavage*) • Activity from 2°C to 37°C • A six-histidine sequence to facilitate its removal from the digested protein sample
Application: Removal of fusion tags from recombinant proteins. Unit Definition: One unit of SUMO Protease is defined as the amount of enzyme needed to cleave 85% of 2μg of substrate protein at 30°C in one hour. Quality Control: SUMO Protease has greater than 85% single-band purity with no non-specific protease contamination. It is functionally tested for the absence of any non-specific protease activity. 5 enzymes
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Host SpeciesS. cerevisiae
Shipping ConditionDry Ice
Quantity250 units
Unit SizeEach
Contents & Storage
SUMO Protease is provided with 10X high salt and 10X no salt dilution buffers. Store at -80°C. Guaranteed stable for 6 months when properly stored.
Frequently asked questions (FAQs)
Are NP40 and DTT required for SUMO Protease activity? Will they interfere with downstream applications?
Yes, they are both required, although it might be possible to substitute the NP40 with another detergent via dialysis if you have concern about interference with mass spectrometry. DTT is an absolute requirement.
What enzyme should I choose if I do not want any extra amino acids left on my protein of interest after cleavage?
SUMO protease, also known as Ulp, is a recombinant fragment of ULP1 (Ubl-specific protease 1) from Saccharomyces cerevisiae. It is highly specific for the SUMO protein fusion, recognizing the tertiary structure of SUMO rather than an amino acid sequence. The SUMO protease itself has a His tag for easy removal from the protein mix after cleavage.