DENARASE® High Salt – Salt-Tolerant Nuclease for High-Efficiency DNA Removal
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c-LEcta GmbH
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c-LEcta GmbH · Verified supplier

DENARASE® High Salt – Salt-Tolerant Nuclease for High-Efficiency DNA Removal

SKU BHZ16500002 · Cat# 20805
In Stock at ManufacturerNewFeaturedGMP AvailablePeer-ReviewedFree Sample

DENARASE® High Salt is designed to retain activity at elevated salt and different pH levels. It is specifically engineered for use in development and manufacturing processes, that benefit from salt additions. The salt-tolerant enzyme efficiently cleaves all forms of DNA and RNA across a broad range of process-relevant conditions, facilitating flexible and more efficient production of biologicals, such as viral vectors and vaccines. DENARASE® High Salt GMP-grade manufacturing complies with EU GMP standards DENARASE® High Salt R&D-grade is produced under ISO 9001 standard Both quality grades of DENARASE® High Salt are technically equivalent, enabling a seamless transition from early R&D stages to biopharmaceutical manufacturing under GMP

At a glance
Purity
≥ 98%
Activity
> 250 U/µL
Salt Range
0–500 mM NaCl
Storage Temperature
-20°C
See all 7 configurations
All configurations · 7 options
Catalog No.SizeQuality GradeAvailability Price Qty Order
22002-25k25 kUR&DIn Stock $363.00
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22002-100k100 kUR&DIn Stock $913.00
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22002-500k500 kUR&DIn Stock $2,744.50
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22002-1000k1000 kUR&DIn Stock $4,015.00
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22002-5000k5000 kUR&DIn Stock $13,579.50
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22002-1M1 MUGMPIn Stock at Manufacturer $4,767.00
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R&D grade: in stock, ships in 2–3 business days. GMP grade: in stock at the manufacturer, 1–2 weeks. Shipped under qualified cooled conditions; transit temperature may differ from storage temperature without affecting quality. −20 °C ± 5 °C. Do not store at −70 °C or below — deep freezing causes loss of activity. Shipping calculated at checkout · card orders +3% · Sales terms & conditions — please review before ordering. For Research Use Only. Not for diagnostic or therapeutic use.
Questions? Talk to us 1-866-986-9598 orders@biohippo.com

Overview

What is denarase® high salt – salt-tolerant nuclease for high-efficiency dna removal?

About DENARASE® High Salt

How DENARASE® High Salt works

DENARASE® High Salt is an engineered version of the wild-type Serratia marcescens endonuclease. By introducing a few targeted amino acid substitutions, the enzyme was optimized for salt tolerance, retaining activity at higher salt concentrations without losing specificity for nucleic acids. DENARASE® High Salt exhibits high DNA removal activity across a broad range of salt concentrations (0–500 mM NaCl) and pH levels, providing greater flexibility in bioprocessing and enabling seamless integration into existing workflows.


Production of DENARASE® High Salt

DENARASE® High Salt is produced using a method nearly identical to the established, patented DENARASE® manufacturing process, based on expression in a gram-positive Bacillus sp. strain. Developed for commercial production of biologicals, the enzyme is manufactured under GMP conditions complying with EU GMP regulations. Produced without antibiotics, Triton X-100, animal-derived or TSE/BSE risk raw materials.


DENARASE® High Salt is available in two quality grades

DENARASE® High Salt for Research and Development (R&D) use & DENARASE® High Salt for manufacturing under GMP.

  • DENARASE® High Salt R&D-grade: produced under ISO 9001 standard; less stringent requirements for documentation, storage, and distribution.
  • DENARASE® High Salt GMP-grade: manufactured under EU GMP conditions; dedicated regulatory support via US FDA Drug Master File.
  • Both quality grades are technically equivalent, enabling a seamless transition from R&D to GMP manufacturing.

Details

Specifications

Alternative namesThe engineered, salt-tolerant variant of DENARASE®, designed for use above 150 mM salt where the standard (wild-type) enzyme loses activity. Serratia marcescens endonuclease. Manufacturer catalogue prefix 22002.
UniProt #P13717 (engineered variant)
SpeciesSerratia marcescens (enzyme origin, salt-tolerant variant)
Expression systemRecombinant, Bacillus sp. (gram-positive)
SourceEngineered salt-tolerant endonuclease expressed in a gram-positive Bacillus sp. host, avoiding the endotoxin burden of gram-negative expression systems. Produced without animal-derived raw materials, antibiotics or Triton X-100.
Molecular weight27 kDa (per monomer)
Purity≥ 98% (SDS-PAGE, silver staining)
Biological activitySpecific activity > 6 × 10⁵ U/mg
Activity> 250 U/µL
Enzyme typeEndonuclease, Salt-tolerant Serratia marcescens nuclease
Endotoxin level< 0.25 EU/kU
Animal origin-freeYes — produced without animal-derived raw materials; no TSE/BSE risk
Antibiotic-freeYes — produced without antibiotics and without Triton X-100
Concentration> 250 U/µL
FormulationBuffered aqueous glycerol solution
pHActive across pH 7.4–9
FormLiquid solution
PackagingNon-pyrogenic, USP Class VI compliant vials; sealed secondary packaging with tamper-evident seals
Storage−20 °C ± 5 °C. Do not store at −70 °C or below — deep freezing causes loss of activity.
Shelf life≥ 12 months when stored at −20 °C ± 5 °C (long-term stability under investigation)
ShippingR&D grade: in stock, ships in 2–3 business days. GMP grade: in stock at the manufacturer, 1–2 weeks. Shipped under qualified cooled conditions; transit temperature may differ from storage temperature without affecting quality.
Unit of measure1 U digests salmon sperm DNA to acid-soluble oligonucleotides equivalent to ΔA₂₆₀ of 1.0 in 30 min at pH 8.0, 37 °C
Catalog no. (Mfr.)20805
Main SKUBHZ16500002

Evidence

Validation & QC

Validation data for this product isn’t published yet.

Need specific QC or validation results — titer, purity, endotoxin, or assay data — for your application? Our scientific team can share what is available for this product and lot on request.

Request validation data

Manufacturing

How it's made & quality control

Supplier quality control

Batch release specification

\nAppearance: clear, transparent solution. Activity above 250 U/µL by photometric assay. Purity ≥ 99% (standard DENARASE®) or ≥ 98% (High Salt) by SDS-PAGE with silver staining. Specific activity above 6 × 10⁵ U/mg. No protease activity detectable. Endotoxin below 0.25 EU/kU by LAL per Ph. Eur. 2.6.14 Method C. Microbial count per Ph. Eur. 2.6.12: aerobic bacteria and yeast or moulds each below 5 cfu per 200 µL.

Clearance validation

\nThe DENARASE® ELISA Kit is a monoclonal antibody-based sandwich ELISA for residual Serratia marcescens endonuclease in process samples, covering standard DENARASE®, DENARASE® High Salt and Benzonase®. Limit of detection 4 pg/mL, limit of quantification 12 pg/mL, working range approximately 32–1,000 pg/mL, assay time approximately 130 minutes. For High Salt, apply a correction factor of 1.46. Benzonase® is a registered trademark of Merck KGaA.

Documents available

\nProduct Information Sheets and Product Specifications for R&D and GMP grades; Validation Guide; guidance on qualifying DENARASE® in biopharmaceutical manufacturing; Change Guidance Document for grade transition; US FDA Drug Master File support documentation; ELISA Kit user instructions, kit contents and prevalidation report.

Supplier-level quality statement. For lot-specific results, request the Certificate of Analysis for your batch.

Questions

Frequently asked questions

What is the difference between DENARASE® and DENARASE® High Salt?

DENARASE® High Salt is an engineered variant of the standard enzyme. A few targeted amino acid substitutions increase salt tolerance without affecting nucleic acid specificity.

Will DENARASE® High Salt replace the standard DENARASE® product?

No. Both products address distinct application needs and will continue to co-exist in the portfolio. The standard enzyme remains the more economical choice below 150 mM salt.

What is the delivery time for DENARASE® High Salt?

R&D grade is held in US stock and ships in 2–3 business days. GMP grade is held at the manufacturer, typically 1–2 weeks.

For which salt concentrations is DENARASE® High Salt recommended?

Above 150 mM NaCl as a general rule. Between 150 and 250 mM, test both enzymes — pH and magnesium concentration also influence activity in this range.

What are the recommended usage conditions?

Recommended for processes above 150 mM NaCl. Magnesium must be raised to at least 5 mM, with a working range of 5–25 mM depending on NaCl and pH; 15 mM is a reasonable starting point for initial tests. Typical starting enzyme concentration is 10–100 U/mL.
Note that the release assay is run at 250 mM NaCl and 5 mM MgCl2, so activity units are not directly comparable to standard DENARASE®. Generate a process-specific activity profile rather than converting between the two.

What can DENARASE® High Salt be used for?

It hydrolyses phosphodiester bonds, leaving fragments of roughly 3–5 base pairs, and is active on all nucleic acid forms — single- and double-stranded, linear, circular and supercoiled. The engineered salt tolerance suits bioprocess steps run at elevated ionic strength.

What are the main application fields?

Viral vector production (AAV, lentivirus, HEK293): used during or after cell lysis in high-salt buffer to reduce viscosity and simplify purification.
Vaccine manufacturing (live attenuated, inactivated, VLP): reduces host cell DNA under elevated ionic strength and improves process robustness.

Are there different quality grades?

Two grades, technically equivalent and released against the same specification parameters. R&D grade is produced under ISO 9001 with less strict documentation, storage and distribution requirements. GMP grade is manufactured under EU GMP with US FDA Drug Master File support and GDP-compliant distribution.

Can the DENARASE® ELISA Kit quantify DENARASE® High Salt?

Yes, but the kit standard is calibrated against standard DENARASE®, so a correction factor of 1.46 must be applied. Alternatively, generate a separate DENARASE® High Salt standard curve. The kit detects residual enzyme down to a limit of quantification of 12 pg/mL.

How can DENARASE® High Salt be removed from my process?

Anion exchange, cation exchange, hydrophobic interaction, hydroxyapatite or size exclusion chromatography, and filtration techniques. Media selection should be evaluated case by case.

How can enzyme activity be inhibited?

NaCl above 1 M is required for inactivation, compared with roughly 600 mM for standard DENARASE®. Potassium phosphate at 200–300 mM also quenches activity, and EDTA above 5 mM inhibits the reaction by removing free magnesium ions.

Are DENARASE® High Salt products tested for endotoxins?

Yes. Every batch must meet the endotoxin specification of less than 0.25 EU/kU before release, tested by LAL assay according to Ph. Eur. 2.6.14 / USP <85> Method C. See the Validation Guide for full details.

How does DENARASE® High Salt compare with other salt-active endonucleases?

c-LEcta has published comparative data covering the development of DENARASE® High Salt and its performance against other commercially available salt-tolerant endonucleases for viral vector manufacturing. Available on request.

Answered by our team

Questions from researchers

No researcher questions have been answered for this product yet. Ask our technical team and we'll get back to you — approved answers are published here.

Ask our technical team

Reviewed by a scientist — typically answered within one business day.

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References

Citations & references

DENARASE® Scientific Publications

A selection of peer-reviewed publications and reports referencing or featuring DENARASE®.

Viral Vectors for Gene Therapy and Vaccine Production

22 publications
Developing a robust and scalable platform for AAV8 production
Nascimento, André et al.
Journal of Biotechnology, Vol. 408, 72–79, December 2025 · doi: 10.1016/j.jbiotec.2025.09.002
View Publication →
Abundance-biased codon diversification prevents recombination in AAV production and ensures robust in vivo expression of functional FRET sensors
Dernic, Jan et al.
Communications Biology vol. 8,1 1244, 19 Aug. 2025 · doi: 10.1038/s42003-025-08677-6
View Publication →
Salt-tolerant endonucleases, the benefits for viral vector manufacturing and a comparison of two marketed enzymes
Marc Struhalla, Svenja Michalek
Cell & Gene Therapy Insights 2025; 11(3), 305–317, 26 March 2025 · doi: 10.18609/cgti.2025.035
View Publication →
Timed chromatin invasion during mitosis governs prototype foamy virus integration site selection and infectivity
Lagadec, Floriane et al.
Nucleic Acids Research vol. 53,10 gkaf449, 31 May 2025 · doi: 10.1093/nar/gkaf449
View Publication →
A two-pass anion-exchange chromatography strategy for enrichment of full capsids in manufacturing of adeno-associated viral vectors
Thakur, Garima et al.
Molecular Therapy. Methods & Clinical Development vol. 33,2 101441, 3 Mar. 2025 · doi: 10.1016/j.omtm.2025.101441
View Publication →
Recombinant AAV batch profiling by nanopore sequencing elucidates product-related DNA impurities and vector genome length distribution
Dunker-Seidler, Florian et al.
Molecular Therapy. Methods & Clinical Development 33,1 101417, 22 Jan. 2025 · doi: 10.1016/j.omtm.2025.101417
View Publication →
Polo-like kinase inhibitors increase AAV production by halting cell cycle progression
Fisher, Kaylin et al.
Molecular Therapy. Methods & Clinical Development vol. 33,1 101412, 17 Jan. 2025 · doi: 10.1016/j.omtm.2025.101412
View Publication →
Selective Enhancement of REM Sleep in Male Rats through Activation of Melatonin MT1 Receptors Located in the Locus Ceruleus Norepinephrine Neurons
López-Canul, Martha et al.
The Journal of Neuroscience vol. 44,29 e0914232024, 17 Jul. 2024
View Publication →
In vivo CAR T-cell generation in nonhuman primates using lentiviral vectors displaying a multidomain fusion ligand
Nicolai, Christopher J et al.
Blood vol. 144,9 (2024): 977–987
View Publication →
Unveiling the secrets of adeno-associated virus: novel high-throughput approaches for the quantification of multiple serotypes
Meierrieks, Frederik et al.
Molecular Therapy. Methods & Clinical Development vol. 31 101118, 2023
View Publication →
Scaling Up of Steric Exclusion Membrane Chromatography for Lentiviral Vector Purification
Labisch et al.
Membranes 13(2): 149 (2023)
View Publication →
Incubation Temperature and Period During Denarase Treatment and Microfiltration Affect the Yield of Recombinant Adenoviral Vectors During Downstream Processing
Sonogür et al.
Molecular Biotechnology 65(7): 1129–1139 (2023)
View Publication →
Efficient clinical-grade γ-retroviral vector purification by high-speed centrifugation for CAR T cell manufacturing
Mekkaoui et al.
Molecular Therapy. Methods & Clinical Development 28: 116–128 (2022)
View Publication →
Comparison of the performance of anion exchange membrane materials for adenovirus purification using laterally-fed membrane chromatography
Kawka et al.
Biochemical Engineering Journal 182: 108417 (2022)
View Publication →
Steric exclusion chromatography of lentiviral vectors using hydrophilic cellulose membranes
Labisch et al.
Journal of Chromatography A 1674: 463148 (2022)
View Publication →
Integrated development of enzymatic DNA digestion and membrane chromatography processes for the purification of therapeutic adenoviruses
Kawka et al.
Separation and Purification Technology 254: 117503 (2021)
View Publication →
A new simplified clarification approach for lentiviral vectors using diatomaceous earth improves throughput and safe handling
Labisch et al.
Journal of Biotechnology 326: 11–20 (2021)
View Publication →
Scalable upstream process development for the suspension-based production of lentiviral vectors for CAR T cell therapies with multiparallel & benchtop bioreactor systems & DoE methodology
Riethmüller et al.
Cell & Gene Therapy Insights 7(6): 689–700 (2021)
View Publication →
Transfer and scale-up from 10 L BioBLU® to Allegro™ STR 50 and STR 200 Bioreactors
Mainwaring et al.
Cell & Gene Therapy Insights 7(9): 1347–1362 (2021)
View Publication →
Scalability comparison between 50 and 500 liter stirred tank bioreactor for production of rAAV viral vector
Sanderson et al.
Cell & Gene Therapy Insights 7(9): 1025–1033 (2021)
View Publication →
Cell culture-based production and in vivo characterization of purely clonal defective interfering influenza virus particles
Hein et al.
BMC Biology 19(1): 91 (2021)
View Publication →
Highly Efficient Purification of Recombinant VSV-ΔG-Spike Vaccine against SARS-CoV-2 by Flow-Through Chromatography
Lerer et al.
BioTech 10(4): 22 (2021)
View Publication →
A high cell density perfusion process for Modified Vaccinia virus Ankara production: Process integration with inline DNA digestion and cost analysis
Gränicher, Gwendal et al.
Biotechnology and Bioengineering 118(12): 4720–4734 (2021)
View Publication →

Production of Virus-like Particles (VLP)

10 publications
Optimizing nuclease treatment to enhance anion exchange chromatography of HIV-derived virus-like particles
M. S. von Elling-Tammen
Journal of Chromatography B vol. 1256 124539, 2025 · doi: 10.1016/j.jchromb.2025.124539
View Publication →
Production of an immunogenic trivalent poliovirus virus-like particle vaccine candidate in yeast using controlled fermentation
Sherry, Lee et al.
NPJ Vaccines 10,1 64, 31 Mar. 2025 · doi: 10.1038/s41541-025-01111-2
View Publication →
Preclinical evaluation of manufacturable SARS-CoV-2 spike virus-like particles produced in Chinese Hamster Ovary cells
Alpuche-Lazcano et al.
Communications Medicine 3(1): 116 (2023)
View Publication →
Development of modern immunization agent against bovine papillomavirus type 1 infection based on BPV1 L1 recombinant protein
Vrablikova et al.
Frontiers in Veterinary Science 10: 1116661 (2023)
View Publication →
Production of antigenically stable enterovirus A71 virus-like particles in Pichia pastoris as a vaccine candidate
Kingston et al.
bioRxiv (Preprint, 2023)
View Publication →
VelcroVax: a "Bolt-On" Vaccine Platform for Glycoprotein Display
Kingston et al.
mSphere 8(1): e0056822 (2023)
View Publication →
Production and Characterisation of Stabilised PV-3 Virus-like Particles Using Pichia pastoris
Sherry et al.
Viruses 14(10): 2159 (2022)
View Publication →
Protease-Independent Production of Poliovirus Virus-like Particles in Pichia pastoris: Implications for Efficient Vaccine Development and Insights into Capsid Assembly
Sherry et al.
Microbiology Spectrum 11(1): e0430022 (2023)
View Publication →
Development and preclinical evaluation of virus-like particle vaccine against COVID-19 infection
Yilmaz et al.
Allergy 77(1): 258–270 (2022)
View Publication →
Separation of influenza virus-like particles from baculovirus by polymer-grafted anion exchanger
Reiter et al.
Journal of Separation Science 43(12): 2270–2278 (2020)
View Publication →

Production of Bacteriophages

2 publications
In situ targeted base editing of bacteria in the mouse gut
Brödel, Andreas K et al.
Nature vol. 632,8026 (2024): 877–884
View Publication →
Phage therapy potentiates second-line antibiotic treatment against pneumonic plague
Vagima et al.
Viruses 14(4): 688 (2022)
View Publication →

Biofilm Removal

2 publications
Targeting Staphylococcus aureus biofilm-related infections on implanted material with a novel dual-action thermosensitive hydrogel containing vancomycin and a tri-enzymatic cocktail: in vitro and in vivo studies
Buzisa Mbuku, Randy et al.
Biofilm vol. 9 100288, 20 May 2025 · doi: 10.1016/j.bioflm.2025.100288
View Publication →
Hydrolytic Enzymes as Potentiators of Antimicrobials against an Inter-Kingdom Biofilm Model
Ruiz-Sorribas et al.
Microbiology Spectrum 10(1): e02589-21 (2022)
View Publication →

Protein Purification

5 publications
Novel fold and wing structure of Forkhead transcription factor facilitate DNA binding
Wang, George L et al.
Nucleic Acids Research vol. 53,18 (2025): gkaf946 · doi: 10.1093/nar/gkaf946
View Publication →
Mapping the genetic landscape of iron metabolism uncovers the SETD2 methyltransferase as a modulator of iron flux
Martinelli, Anthony W et al.
Science Advances vol. 11,38 (2025): eadw9095 · doi: 10.1126/sciadv.adw9095
View Publication →
Granulins rescue inflammation, lysosome dysfunction, lipofuscin, and neuropathology in a mouse model of progranulin deficiency
Root, Jessica et al.
Cell Reports 43,12 (2024): 114985 · doi: 10.1016/j.celrep.2024.114985
View Publication →
Effective removal of host cell-derived nucleic acids bound to hepatitis B core antigen virus-like particles by heparin chromatography
Valentic, Angela, and Jürgen Hubbuch
Frontiers in Bioengineering and Biotechnology 12 1475918, 3 Oct. 2024 · doi: 10.3389/fbioe.2024.1475918
View Publication →
Deubiquitinating enzyme mutagenesis screens identify a USP43-dependent HIF-1 transcriptional response
Pauzaite, Tekle et al.
The EMBO Journal vol. 43,17 (2024)
View Publication →

Customization

Customization & add-ons

Many enzymes can be supplied in formats beyond the catalog listing — alternative grades (research versus GMP/manufacturing), glycerol-free or custom buffers, defined activity units or concentrations, and bulk or large-scale quantities. Custom formulation and packaging are available for selected products. Availability, minimum order quantities, and lead times vary by supplier. Tell us the enzyme, the grade, formulation, and activity you need, and the scale, and we’ll prepare a quote.
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Try Celltrypse Free – Request Your Sample Today

Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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