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Merck

E1014

Nucleasas Benzonase®

≥250 units/μL, ≥90% (SDS-PAGE), recombinant, expressed in E. coli, buffered aqueous glycerol solution

Benzonase® Nuclease

Sinónimos:

Endonucleasas from Serratia marcescens

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5 KU

US$ 115,00

25 KU

US$ 408,00

US$ 115,00

PRECIOS SIN IMPUESTOS NACIONALES

Fecha estimada de envío09 de marzo de 2026Detalles


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Número CAS:
UNSPSC Code:
12352204
NACRES:
NA.54
Número CE:
MDL number:
Assay:
≥90% (SDS-PAGE)
Biological source:
Serratia marcescens
Recombinant:
expressed in E. coli
Concentration:
≥250 units/μL

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biological source

Serratia marcescens

recombinant

expressed in E. coli

assay

≥90% (SDS-PAGE)

form

buffered aqueous glycerol solution

mol wt

30 kDa

concentration

≥250 units/μL

application(s)

research use

foreign activity

protease, essentially free

shipped in

wet ice

storage temp.

−20°C

Quality Level

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1 of 4

Este artículo
706647120671205-M
assay

≥90% (SDS-PAGE)

assay

>99% (SDS-PAGE)

assay

>99% (SDS-PAGE)

assay

>90% (SDS-PAGE)

biological source

Serratia marcescens

biological source

Serratia marcescens

biological source

Serratia marcescens

biological source

Serratia marcescens

form

buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

application(s)

research use

application(s)

research use

application(s)

research use

application(s)

research use

concentration

≥250 units/μL

concentration

25-29 units/μL

concentration

≥250 units/μL

concentration

≥250 units/μL

recombinant

expressed in E. coli

recombinant

expressed in E. coli

recombinant

expressed in E. coli

recombinant

expressed in E. coli

General description

La nucleasa Benzonase® es una endonucleasa genotecnológica muy eficiente procedente de Serratia marcescens[1]. Este dímero proteico con dos enlaces disulfuro esenciales [2] es capaz de atacar y degradar todas las formas de ADN y ARN (monocatenarias, bicatenarias, lineales y circulares) en una amplia variedad de condiciones de funcionamiento. La nucleasa Benzonase® es capaz de eliminar los ácidos nucleicos y potenciar la pureza y la calidad de las muestras proteicas.

Application

Utilizado para eliminación de los ácidos nucleicos de las muestras proteicas.
La nucleasa Benzonase® se ha utilizado: como un componente del amortiguador C de lisis en frío para digerir el ADN y  el ARN y facilitar así la liberación completa de todas las proteínas nucleares en el paso de inmunoprecipitación para liberar los complejos proteicos del nucleoplasma y la cromatina como un suplemento en RIPA para fraccionar las células SHSY5Y destinadas a inmunoprecipitación para eliminar los ácidos nucleicos residuales de las raíces aórticas en el método de descelularización

Biochem/physiol Actions

Digiere el ADN y el ARN nativos o desnaturalizados por calor.
La nucleasa Benzonase® puede digerir por completo los ácidos nucleicos en oligonucleótidos de 3 a 5 bases de longitud terminados en 5′-monofosfato, lo que la convierte en la herramienta ideal para separar los ácidos nucleicos de las proteínas recombinantes y para aplicaciones que requieran una digestión completa de los ácidos nucleicos. Además de reducir la viscosidad en los extractos de proteínas y evitar la aglutinación celular, el pretratamiento de muestras proteicas con las nucleasas Benzonase® puede mejorar significativamente su resolución en la electroforesis bidimensional en gel al eliminar cualquier ácido nucleico unido. Esta enzima versátil puede digerir el ADN y el ARN nativos o desnaturalizados por calor con su pH de actividad enzimática óptimo que oscila entre 8,0 y 9,2. La nucleasa Benzonase® elimina con eficacia el ADN huésped de las muestras de microbioma. En muchos casos, las muestras de microbioma (como la saliva o la piel) tendrán un elevado porcentaje de ADN del huésped que interfiere en los resultados posteriores. Nuestros expertos demuestran que la reducción del ADN del huésped disminuye el coste de la secuenciación al tiempo que aumenta y mejora los datos. Encontrará los datos experimentales en el artículo técnico - Benzonase® Nuclease for Microbiome Workflows

Features and Benefits

  • Eliminación del ADN del huésped en muestras de microbioma.


  • Digestión eficaz del ácido nucleico en una variedad de procedimientos de trabajo.


  • Reducción de la viscosidad durante la extracción de proteínas.

Physical form

Disolución en glicerol al 50% que contenga Tris HCl 20 mM, pH 8,0, MgCl2 2 mM y NaCl 20 mM.

Other Notes

Una unidad digerirá el ADN de esperma de salmón tratado con ultrasonidos a oligonucleótidos solubles en ácido equivalentes a ΔA260 de 1,0 en 30 minutos a pH 8,0 a 37 °C (volumen de reacción 2,625 ml).

Legal Information

La nucleasa Benzonase® es suministrada por Merck KGaA, Darmstadt, Alemania y sus filiales.
Benzonase is a registered trademark of Merck KGaA, Darmstadt, Germany

Clase de almacenamiento

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves


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Certificados de análisis (COA)

Lot/Batch Number

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Sequential fractionation and isolation of subcellular proteins from tissue or cultured cells
Baghirova S, et al.
MethodsX, 2, 440-445 (2015)
The involvement of tau in nucleolar transcription and the stress response
Maina M.B., et al.
Acta Neuropathologica Communications, 6(70) (2018)
Characterization of Laminins in Healthy Human Aortic Valves and a Modified Decellularized Rat Scaffold
Granath C, et al.
BioResearch Open Access, 9(1) (2020)
P Friedhoff et al.
Protein expression and purification, 5(1), 37-43 (1994-02-01)
Overproduction of the extracellular Serratia marcescens nuclease in Escherichia coli results in aggregation and sequestration of a large amount of the protein in inclusion bodies. Only a relatively small amount is secreted into the medium from which it can be
Richik Nilay Mukherjee et al.
Molecular biology of the cell, 30(18), 2349-2357 (2019-07-19)
Endoplasmic reticulum (ER) tubules and sheets conventionally correspond to smooth and rough ER, respectively. The ratio of ER tubules-to-sheets varies in different cell types and changes in response to cellular conditions, potentially impacting the functional output of the ER. To

Artículos

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

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

This discussion will highlight some of these methodologies, namely, the use of Multiple Reaction Monitoring (MRM) and Protein-AQUA.

Benzonase® Nuclease for reducing host DNA in microbiome workflows and enhancing taxa identification.

Contenido relacionado

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The use of Benzonase® endonuclease can significantly reduce the levels of DNA by more than 100,000-fold while also reducing viscosity and protecting downstream equipment from DNA fouling. However, optimization strategies and DoE are critical when it comes to reducing DNA in your process. Setting up a DoE for your Benzonase® endonuclease application can help you find the optimal operation conditions that deliver the required DNA clearance from your process.

Questions

1–8 of 8 Questions  
  1. hi, I received E1014-5KU product. I couldn't find what solution should I dilute to get a concentration of 25U/ml. Also, the volume of the solution.

    1 answer
    1. The actual volume of the solution is determined by the lot-specific activity, which can be found in the Certificate of Analysis. For this product, there are 5,000 units available. If the lot has a specific activity of 335 U/?L, the volume will be approximately 14.9 ?L for 5,000 units. It is recommended to dilute the product in 20 mM Tris-HCl (pH 8.0), 2 mM MgCl?, and 20 mM NaCl.

      Helpful?

  2. Do you sell high salt lysis buffers that are compatible with benzonase? Do you have any written protocols for use of benzonase with high salt buffers?

    1 answer
    1. We do not have a branded "high-salt lysis buffer" off the shelf that is compatible with benzonase. However, we offer a specialized Benzonase® Salt Tolerant Endonuclease which is active at higher salt concentration, up to1M NaCl .
      https://www.sigmaaldrich.com/US/en/product/mm/e5014

      Helpful?

  3. I am doing a protein purification and would like to know if magnesium chloride is required in the lysis buffer when using the Benzonase. Also, would the activity of benzonase be affected when added to a lysis buffer containing EDTA

    1 answer
    1. A concentration of 1-2 mM of magnesium is required for the activity of this product. An EDTA concentration of 1 mM partially inhibits the activity of this product.

      Helpful?

  4. Hi, what is the ratio of E1014 : DNA and E1014 : RNA for an efficient acid nucleic removal?

    1 answer
    1. For efficient nucleic acid removal using Benzonase® (E1014), the recommended ratio depends on the concentration of DNA or RNA in the sample. A typical starting point is 25 U/mL of Benzonase® for reducing nucleic acid content in lysates, which corresponds to approximately 1 unit of enzyme per 37 µg of DNA under optimal conditions. For lower concentrations of DNA or RNA, as little as 9 U/mL may achieve 99% removal, but higher concentrations, e.g., 90 U/mL, ensure faster and more complete degradation. Optimal activity requires 1–2 mM magnesium ions, a pH of 8.0–9.2, and incubation at 37°C. Adjustments may be needed for sample-specific factors such as buffer composition and nucleic acid load.

      Helpful?

  5. How many ul does it contain? What kind of Unit is KU?

    1 answer
    1. The unit activity of this product is lot-specific and reported in the product Certificate of Analysis. The minimum activity is 250 units per microliter. The KU value represents 1000 units. For example, a 20 KU package size represents 20,000 units. Please see the link below to review a sample or lot-specific Certificate:
      https://www.sigmaaldrich.com/product/sigma/e1014#product-documentation

      Helpful?

  6. Hi, for protein purification from E. coli cells, how much is the working concentration range for Benzonase nuclease (≥250 units/μL)? Thank you 

    1 answer
    1. The recommended starting concentration for Benzonase nuclease is 25 units per milliliter of cell lysate.

      Helpful?

  7. Hello, I plan to do proteomic for protein. When I add RIPA buffer to isolate the protein, I need to remove the DNA and RNA inside. When should I add E1014? Together with RIPA or after it?

    1 answer
    1. Concentrations greater than 1 mM EDTA will inhibit Benzonase activity, and RIPA buffer recipes typically contain EDTA at higher concentrations than 1 mM. Therefore, Benzonase should be used after removing EDTA from the lysed sample or consider using a different lysis solution that does not include EDTA in the formulation.

      Helpful?

  8. What is the storage temperature range for E1014? There is only a specified storage temperature, and not a range.

    1 answer
    1. This product is stored at freezer temperature, which is typically -20°C. An excepted range is -15 - -20°C.

      Helpful?

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