MinuteCut Kas Ⅰ Instructions

MinuteCutTM restriction enzyme has been genetically engineered and recombinant, and can quickly and accurately complete DNA digestion in 5~15 min.

MinuteCut Kas Ⅰ Instructions

Suitable for rapid digestion of plasmid DNA, PCR products, or genomic DNA.
The dephosphorylated, ligation reagent is 100% active in MinuteCutTM digestion buffer.
It supports one-tube reaction to improve the experience of “digestion-modification-ligation”.

Price List

Product No Quantity Price
6033025 25 preps contact us

Storage

This product can be stored at -20℃ for up to 2 years.

Technical Support

R&D Department, Hangzhou Simgen Biotechnology Co., Ltd. E-mail: technical@simgen.cn, Tel: 400-0099-857.

Introduction

MinuteCutTM enzymes are a series of engineered restriction enzymes that are capable of fast DNA digestion. All MinuteCutTM enzymes show superior activity in the universal 10×MinuteCutTM Buffer and 10×MinuteCutTM Red Buffer and are able to digest DNA in 5~15 min. This enables any combination of restriction enzymes to work simultaneously in one reaction tube and eliminates the need for sequential digestions. MinuteCutTM enzymes have passed multiple strict quality controls, and can be used to digest plasmid, genomic and viral DNA as well as PCR products. 10×MinuteCutTM Red Buffer includes a density reagent along with red and yellow tracking dyes that allow for direct loading of the reaction mixtures on a gel. The red dye of the 10×MinuteCutTM Red Buffer migrates with 2.5 kb double-strand DNA fragments in a 1% agarose gel, and the yellow dye migrates with 10 bp double-strand DNA fragments in a 1% agarose gel.

Definition of Activity Unit

One unit of activity refers to the amount of enzyme required to completely digest 1 µg of pBR322 in a 50 μl reaction system at 37℃ for 1 hour.

Quality Control

Prolonged Incubation/Star Activity Assay

Under optimal reaction temperature, incubate 10 U Kas Ⅰ with 1 μg pBR322 for 16 hours. No contamination from other nucleases or nonspecific substrate degradation caused by star activity was detected. Longer incubation may result in star activity.

Ligation and Recutting

Under optimal reaction temperature, digest the substrate using 10 U Kas Ⅰ and recover the digested products. >95% of the DNA fragments can be ligated with T4 DNA Ligase at 22℃ .Of these ligated fragments, >95% can be recut with Kas Ⅰ as determined by agarose gel electrophoresis

Resources

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