製品名
エンドヌクレアーゼ Serratia marcescens(セラチア菌)由来, Effective viscosity reduction and removal of nucleic acids from protein solutions
biological source
Serratia marcescens
recombinant
expressed in E. coli
assay
>99% (SDS-PAGE)
form
buffered aqueous glycerol solution
manufacturer/tradename
Novagen®
storage condition
OK to freeze
concentration
25-29 units/μL
impurities
<0.25 EU/kU Total endotoxin
application(s)
research use
shipped in
wet ice
storage temp.
−20°C
Quality Level
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関連するカテゴリー
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。
Disclaimer
Toxicity: Standard Handling (A)
General description
Benzonase® Nuclease is a genetically engineered endonuclease from Serratia marcescens. It degrades all forms of DNA and RNA (single stranded, double stranded, linear and circular) while having no proteolytic activity. It is effective over a wide range of conditions and possesses an exceptionally high specific activity. The enzyme completely digests nucleic acids to 5′-monophosphateterminated oligonucleotides 2 to 5 bases in length (below the hybridization limit), which is ideal for removal of nucleic acids from recombinant proteins, enabling compliance with FDA guidelines for nucleic acid contamination. The ability of Benzonase to rapidly hydrolyze nucleic acids makes the enzyme an excellent choice for viscosity reduction to reduce processing time and increase yields of protein. For example, the enzyme is compatible with BugBuster and PopCulture Protein Extraction Reagents and can therefore be added along with these reagents to eliminate viscosity and remove nucleic acids from E. coli extracts.
The enzyme consists of two subunits of30 kDa each. It is functional between pH 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 (relative activity depends on specific conditions).Activity is inhibited by > 150 mM monovalent cations, > 100 mM phosphate, > 100 mMammonium sulfate, or > 100 mM guanidine HCl.
Benzonase Nuclease is available in ultrapure (> 99% by SDS-PAGE) and pure (> 90%) grades at a standard concentration of 25-29 U/µl and at a high concentration (HC) of 250 U/µl. Both preparations are free of detectable protease and have specific activity> 1 × 106 U/mg protein. The > 99% purity grade is tested for endotoxins and contains< 0.25 EU/1000 units. The product is supplied in 50% glycerol. Store at -20°C.

Total endotoxin:< 0.25 EU/1,000 units. Purity: > 99% by SDS-PAGE.
The enzyme consists of two subunits of30 kDa each. It is functional between pH 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 (relative activity depends on specific conditions).Activity is inhibited by > 150 mM monovalent cations, > 100 mM phosphate, > 100 mMammonium sulfate, or > 100 mM guanidine HCl.
Benzonase Nuclease is available in ultrapure (> 99% by SDS-PAGE) and pure (> 90%) grades at a standard concentration of 25-29 U/µl and at a high concentration (HC) of 250 U/µl. Both preparations are free of detectable protease and have specific activity> 1 × 106 U/mg protein. The > 99% purity grade is tested for endotoxins and contains< 0.25 EU/1000 units. The product is supplied in 50% glycerol. Store at -20°C.

Total endotoxin:< 0.25 EU/1,000 units. Purity: > 99% by SDS-PAGE.
Effective viscosity reduction and removal of nucleic acids from protein solutions
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
保管分類
10 - Combustible liquids
wgk
WGK 2
試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
Hannah Schneider et al.
Journal of neurochemistry, 140(1), 170-182 (2016-10-28)
Targeting the vascular endothelial growth factor signaling axis in glioblastoma inevitably leads to tumor recurrence and a more aggressive phenotype. Therefore, other angiogenic pathways, like the angiopoietin/tunica interna endothelial cell kinase (TIE) signaling axis, have become additional targets for therapeutic
Xuemei Nan et al.
Physiological genomics, 46(7), 268-275 (2014-01-30)
This study was conducted to determine the optimum ratio of lysine and methionine (Lys:Met) to enhance milk protein concentration in vitro, focusing on the regulation of genes related to the JAK2-STAT5 and the mammalian target of rapamycin (mTOR) signaling pathways.
Enmanuel J Perez et al.
The Journal of clinical investigation, 127(8), 3114-3125 (2017-07-18)
After traumatic brain injury (TBI), glial cells have both beneficial and deleterious roles in injury progression and recovery. However, few studies have examined the influence of reactive astrocytes in the tripartite synapse following TBI. Here, we have demonstrated that hippocampal
Timothy N Audam et al.
American journal of physiology. Heart and circulatory physiology, 319(1), H109-H122 (2020-05-23)
Although cell therapy-mediated cardiac repair offers promise for treatment/management of heart failure, lack of fundamental understanding of how cell therapy works limits its translational potential. In particular, whether reparative cells from failing hearts differ from cells derived from nonfailing hearts
Georg E Winter et al.
Molecular cell, 67(1), 5-18 (2017-07-05)
Processive elongation of RNA Polymerase II from a proximal promoter paused state is a rate-limiting event in human gene control. A small number of regulatory factors influence transcription elongation on a global scale. Prior research using small-molecule BET bromodomain inhibitors
資料
Benzonase®endonuclease efficiently removes nucleic acid contaminants from viral production, crucial for cell and gene therapies and vaccines.
グローバルトレードアイテム番号
| カタログ番号 | GTIN |
|---|---|
| 70664-3CN | 07790788052751 |
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