CAS 9025-65-4

endonuclease serratia marcescens,*recombinant 90+

Description:

Endonuclease Serratia marcescens, recombinant 90+ (CAS 9025-65-4) is an enzyme derived from the bacterium Serratia marcescens, known for its role in nucleic acid metabolism. This enzyme exhibits endonuclease activity, meaning it can cleave the phosphodiester bonds within nucleic acids, such as DNA and RNA, thereby facilitating processes like DNA repair, replication, and degradation. The "recombinant" designation indicates that the enzyme is produced through recombinant DNA technology, allowing for the generation of large quantities with specific activity and purity. Endonuclease Serratia marcescens is characterized by its ability to function optimally under certain pH and temperature conditions, which can vary based on the specific recombinant strain used. It is commonly utilized in molecular biology applications, including cloning, sequencing, and the preparation of nucleic acids for various assays. Additionally, this enzyme is valued for its specificity and efficiency, making it a crucial tool in genetic engineering and biotechnological research.

Synonyms:

• Binuclease(substitute of Benzonase)

Endonuclease (Serratia marcescens) (35 uL)

CAS: 9025-65-4

Enzymes and prepared enzymes, nesoi

Color and Shape: Clear Liquid

Ref: 45-1235470

Serratia marcescens nuclease

CAS: 9025-65-4

Serratia marcescens nuclease is a non-specific endonuclease used in molecular biology to degrade and remove DNA and RNA.

Color and Shape: Solid

Ref: TM-T78347

HL-Nuclease

CAS: 9025-65-4

Ref: 7W-GZ3821

Ultra nuclease, liquid, recombinant

CAS: 9025-65-4

Ultra nuclease (EC 3.1.30.2) is an enzyme that digests DNA and RNA in any form: single- and double-stranded, linear, circular and supercoiled. The ultimate reaction product is 5'-monophosphate oligonucleatides that are mostly three, four and five bases long. Please enquire for more information about Ultra nuclease, liquid, recombinant including the price, delivery time and more detailed product information at the technical inquiry form on this page

Ref: 3D-ETS007.7

Endonuclease, liquid, food grade

CAS: 9025-65-4

Endonuclease, liquid, food grade is a biochemical enzyme, which is derived from microbial or bovine sources, with precision in hydrolyzing phosphodiester bonds within nucleic acids. This endonuclease cleaves the internal bonds of DNA and RNA, enabling the breakdown of these molecules into smaller nucleotide fragments. Its catalytic action is particularly useful in the controlled degradation of nucleic acids without affecting other macromolecules in the substrate.

Ref: 3D-ETS022.7

eXrase DNA Endonuclease, research-grade

CAS: 9025-65-4

eXrase DNA endonuclease from enGenes is a recombinant endonuclease from Serratia marcescens produced in E. coli. Effectively and efficiently degrades all forms of DNA and RNA, reducing sample viscosity without proteolytic activity. As effective and efficient as other nucleases on the market, eXrase DNA endonuclease is the most cost-effective way to improve proteins yields and improve sample handing. Presented as a ready to use colourless liquid, formulated in Tris buffer at pH 8.0 with 50 % glycerol (v/v).  This research grade eXrase has low endotoxin, max 0.25 EU/kU.eXrase DNA endonuclease is suitable for the effective breakdown of nucleic acids in numerous biotech settings:  • Removal of residual host DNA from biotechnological products to meet regulatory standards • Reduction of viscosity and streamlined purification in downstream processing of fermentation procedures. • Reduction of viscosity in in upstream fermentation processes • Extraction and/or synthesis of flavouring nucleotides • Enhanced bioavailability of nucleotides in specific feed products • DNA degradation for the removal or prevention of biofilm formationeXrase DNA endonuclease from enGenes is made by a proprietary microbial fermentation process utilizing Escherichia coli cells. This enzyme facilitates the hydrolysis of phosphodiester bonds in various forms of DNA and RNA, including single-stranded, double-stranded, linear, circular, or supercoiled configurations, yielding smaller oligonucleotides typically composed of 2-4 base pairs. Unit-Definition: One unit (U) of the enzyme is defined as the amount required to digest calf thymus DNA, yielding acid-soluble oligonucleotides equivalent to a ΔA260nm of 1.0 within a 30-minute timeframe at pH 8.0 and 37°C. This standardization allows for consistent measurement of enzymatic activity across different batches.

Ref: 3D-EXR-RG

eXrase DNA Endonuclease, tech-grade

CAS: 9025-65-4

eXrase DNA endonuclease from enGenes is a recombinant endonuclease from Serratia marcescens produced in E. coli. Effectively and efficiently degrades all forms of DNA and RNA, reducing sample viscosity without proteolytic activity. As effective and efficient as other nucleases on the market, eXrase DNA endonuclease is the most cost-effective way to improve proteins yields and improve sample handing. Presented as a ready to use colourless liquid, formulated in Tris buffer at pH 8.0 with 50 % glycerol (v/v). This tech grade version is our most cost effective endonuclease for R&D applications. eXrase DNA endonuclease is suitable for the effective breakdown of nucleic acids in numerous biotech settings:  • Removal of residual host DNA from biotechnological products to meet regulatory standards • Reduction of viscosity and streamlined purification in downstream processing of fermentation procedures. • Reduction of viscosity in in upstream fermentation processes • Extraction and/or synthesis of flavouring nucleotides • Enhanced bioavailability of nucleotides in specific feed products • DNA degradation for the removal or prevention of biofilm formationeXrase DNA endonuclease from enGenes is made by a proprietary microbial fermentation process utilizing Escherichia coli cells. This enzyme facilitates the hydrolysis of phosphodiester bonds in various forms of DNA and RNA, including single-stranded, double-stranded, linear, circular, or supercoiled configurations, yielding smaller oligonucleotides typically composed of 2-4 base pairs. Unit-Definition: One unit (U) of the enzyme is defined as the amount required to digest calf thymus DNA, yielding acid-soluble oligonucleotides equivalent to a ΔA260nm of 1.0 within a 30-minute timeframe at pH 8.0 and 37°C. This standardization allows for consistent measurement of enzymatic activity across different batches.

Ref: 3D-EXR-TG