Product Number: RE0610
Shipping and Storage
-20±5℃
Description
Restriction endonucleases, abbreviated as restriction enzymes, are a type of nucleic acid endonuclease that can recognize specific deoxyribonucleotide sequences and cleave the phosphodiester bond between two deoxyribonucleotides at specific positions in each strand. Restriction enzymes are an important component of the "restriction modification system", whose biological function is mainly to protect the host from infection by foreign DNA. They are widely used in various fields such as gene localization and cloning, gene structure research, DNA sequence analysis and determination, gene synthesis, etc. BspQI is derived from the BspQI gene of Bacillus sphaericus and is a commonly used IIS type restriction endonuclease.
This product is produced using recombinant protein production technology to obtain BspQI, using pharmaceutical grade raw materials and strictly controlling host protein residues, nucleic acid residues, etc. It complies with GMP standards for product production and quality management regulations, ensuring that all raw materials in the production process are traceable.
Application
Linearization of in vitro transcription templates; Molecular cloning; Genotyping; Southern hybridization; SNP; Restriction fragment length polymorphism (RFLP).
Quality control
Project | Specification |
Appearance | Clear liquid |
Visible foreign matter | Compliance |
pH | 6.5-7.5 |
Reactivity | 10U/μL-12.5U/μL |
Residual endonuclease | The degradation of substrates shall not exceed 10% |
Residual exonuclease of nucleic acid | The degradation of substrates shall not exceed 10% |
RNA enzyme residue | The degradation of substrates shall not exceed 10% |
Bacterial endotoxin | < 10EU/mL |
Microbial limit | The total number of aerobic bacteria should not exceed 1cfu/10mL, and the total number of mold and yeast should not exceed 1cfu/10mL |
Features
5’... GCTCTTC(N)1↓... 3’
3’... CGAGAAG(N)4↑... 5’
Definition of Activity
Under the conditions of 50℃ and pH 7.0, complete digestion of 1μg of λ DNA within 1 hour is defined as 1 active unit.
Preservation system
20mM Tris-HCl; 500mM KCl; 1mM DTT; 0.1mM EDTA; 0.1% Triton X-100;50% Glycerol; pH 7.0 at 25℃.