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Merck

70746

Benzonase® Nuclease

Purity > 90%

別名:

Endonuclease from Serratia marcescens

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この商品について

CAS番号:
UNSPSC Code:
12352202
NACRES:
NA.54
EC Number:
MDL number:
Assay:
>90% (SDS-PAGE)
Biological source:
Serratia marcescens
Recombinant:
expressed in E. coli
Concentration:
25-29 units/μL
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製品名

エンドヌクレアーゼ Serratia marcescens(セラチア菌)由来,

biological source

Serratia marcescens

Quality Level

recombinant

expressed in E. coli

assay

>90% (SDS-PAGE)

form

buffered aqueous glycerol solution

manufacturer/tradename

Novagen®

storage condition

OK to freeze

concentration

25-29 units/μL

application(s)

research use

shipped in

wet ice

storage temp.

−20°C

General description

Benzonase® Nuclease is a geneticallyengineered endonuclease from Serratiamarcescens. It degrades all forms of DNA andRNA (single stranded, double stranded, linearand circular) while having no proteolyticactivity. It is effective over a wide range ofconditions and possesses an exceptionallyhigh specific activity. The enzyme completelydigests nucleic acids to 5′-monophosphateterminated oligonucleotides 2 to 5 bases inlength (below the hybridization limit), whichis ideal for removal of nucleic acids fromrecombinant proteins, enabling compliancewith FDA guidelines for nucleic acidcontamination. The ability of Benzonase torapidly hydrolyze nucleic acids makes theenzyme an excellent choice for viscosityreduction to reduce processing time andincrease yields of protein. For example, theenzyme is compatible with BugBuster andPopCulture Protein Extraction Reagentsand can therefore be added along with thesereagents to eliminate viscosity and removenucleic acids from E. coli extracts.

The enzyme consists of two subunits of30 kDa each. It is functional betweenpH 6 and 10 and from 0-42°C and requires1-2 mM Mg2+ for activation. The enzyme is also active in the presence of ionic and non-ionic detergents, reducing agents, PMSF(1 mM), EDTA (1 mM) and urea (relativeactivity depends on specific conditions).Activity is inhibited by >150 mM monovalentcations, >100 mM phosphate, >100 mMammonium sulfate, or >100 mM guanidine HCl.

Benzonase Nuclease is available inultrapure (>99% by SDS-PAGE) and pure(>90%) grades at a standard concentrationof 25-29 U/µl and at a high concentration (HC)of 250 U/µl. Both preparations are free ofdetectable protease and have specific activity> 1 × 106 U/mg protein. The >99% puritygrade is tested for endotoxins and contains<0.25 EU/1000 units. The product is suppliedin 50% glycerol.Store at -20°C.

Total endotoxin:<0.25 EU/1,000 units.Purity: >90% by SDS-PAGE

Application

タンパク質サンプルから核酸を除去する際に使用します。

Biochem/physiol Actions

未変性または熱変性のDNA, RNAを分解します。

Other Notes

One unit is defined as the amount of enzyme that causes a ΔA₂₆₀ of 1.0 in 30 minutes, which corresponds to complete digestion of 37 µg DNA.

Legal Information

Benzonase is a registered trademark of Merck KGaA, Darmstadt, Germany
NOVAGEN is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Standard Handling (A)


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保管分類

10 - Combustible liquids



試験成績書(COA)

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資料

Benzonase®endonuclease efficiently removes nucleic acid contaminants from viral production, crucial for cell and gene therapies and vaccines.

このページは、Benzonase®(ベンゾナーゼ)ヌクレアーゼについてよくある質問9項目とその回答をまとめたものです。

This page lists nine frequently asked questions and answers about Benzonase® Nuclease.

すべての記事を見る

Benjamin Strobel et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 23(10), 1582-1591 (2015-07-04)
Cytotoxicity of transgenes carried by adeno-associated virus (AAV) vectors might be desired, for instance, in oncolytic virotherapy or occur unexpectedly in exploratory research when studying sparsely characterized genes. To date, most AAV-based studies use constitutively active promoters (e.g., the CMV
Mark A Kanow et al.
eLife, 6 (2017-09-14)
Here we report multiple lines of evidence for a comprehensive model of energy metabolism in the vertebrate eye. Metabolic flux, locations of key enzymes, and our finding that glucose enters mouse and zebrafish retinas mostly through photoreceptors support a conceptually
Jonathan Barroso-González et al.
Molecular cell, 76(1), 11-26 (2019-08-12)
Alternative lengthening of telomeres (ALT) is a homology-directed repair (HDR) mechanism of telomere elongation that controls proliferation in aggressive cancers. We show that the disruption of RAD51-associated protein 1 (RAD51AP1) in ALT+ cancer cells leads to generational telomere shortening. This



グローバルトレードアイテム番号

カタログ番号GTIN
70746-4CN04055977256949
70746-3CN07790788052805