Endonuclease VIII (10 U/μL)

SKU:BHZ20800094 Enzymes & Molecular Biology
Overview
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Endonuclease VIII is a DNA repair enzyme that possesses both N-glycosylase activity and AP-lyase activity. The N-glycosylase activity can release damaged pyrimidine bases from double-stranded DNA, creating an abasic (AP) site. The AP-lyase activity then cleaves the phosphodiester bond at the AP site
Enzyme Type Nucleases
Grade RUO
Storage -20°C
Shipping Dry Ice
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options:
    • Size (2) - 1000 U, 5000 U
  • Lead time: options listed in "Availability Content"; otherwise, there will be a column of "lead time", other statuses may take longer.
  • Storage: -20°C
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible.
  • Sales terms and conditions: Please review prior to ordering.
Options selector
Catalog no. Size
14536ES80 1000 U
14536ES90 5000 U
Field Specification
Product Type
  • Enzymes
  • Nucleases
Shipping Dry Ice
Source Recombinant (E. coli)
Storage -20°C

Endonuclease VIII is a DNA repair enzyme that possesses both N-glycosylase activity and AP-lyase activity. The N-glycosylase activity can release damaged pyrimidine bases from double-stranded DNA, creating an abasic (AP) site. The AP-lyase activity then cleaves the phosphodiester bond at the AP site, resulting in a gap with a 5' phosphate and a 3' phosphate. The damaged bases that Endonuclease VIII recognizes and excises include: urea, 5,6-dihydroxythymine, thymine glycol, 5-hydroxy-5-methoxyhydantoin, uracil glycol, 6-hydroxy-5,6-dihydrothymidine, and methylhydroxypropanone.

Features

No residual of exonucleases, endonucleases, or RNases

High-efficiency removal of damaged bases

Applications

Single-cell gel electrophoresis (Comet assay)

Alkaline elution

Alkaline unwinding

Specifications

Source

E. coli

Molecular Weight

29 KDa

Concentration

10 U/μL

Unit Definition

One unit is defined as the amount of enzyme required to cleave 1 pmol of a 34 bp oligonucleotide duplex containing one AP site* in a 10 µL total reaction system with 10 pmol of fluorescently labeled oligonucleotide duplex in 1X Endonuclease VIII Reaction buffer at 37°C within 1 hour

Inactivation Conditions

Incubate at 75°C for 10 minutes

Glycerol Content

Contains Glycerol

Components

Components No.

Name

14536ES80

14536ES90

14536-A

Endonuclease VIII(10 U/μL)

100 μL

500 μL

14536-B

10 × Endonuclease VIII Reaction Buffer

1.5 mL

1.5 mL

Shipping and Storage

The products should be stored at -25℃ ~ -15℃ for 1 year.

Figures

Figure1. Base excision repair effect comparison

Note: 20 pmol of oligonucleotides were catalyzed by Endonuclease VIII from Yeasen and SupplierA, respectively, in a 20 µL reaction system with the addition of 5~40 U of Endonuclease VIII and equivalent enzyme activity of UDG (Cat#10303ES), and incubated at 37 for 1 hour. The results of agarose gel electrophoresis showed that the base excision effects of Yeasen 's Endonuclease VIII and Supplier A's were consistent.

Store this enzyme at -20°C and avoid repeated freeze-thaw cycles to preserve catalytic activity. The product is shipped Dry Ice and remains stable for up to one year from the date of manufacture when stored under recommended conditions. Aliquoting the stock solution into single-use volumes is recommended for enzymes used infrequently to minimize thermal cycling of the bulk stock.

Single-cell gel electrophoresis (Comet assay) Alkaline elution Alkaline unwinding. Always verify compatibility with your specific template, buffer, and downstream workflow.

One unit (U) is defined as the amount of enzyme that degrades 1 µg of DNA or RNA substrate to acid-soluble form in 30 min at 37°C under defined buffer conditions.

This enzyme is produced as Recombinant (E. coli) and supplied as a Research Use Only (RUO) reagent. Each lot is subjected to activity assay, purity assessment by SDS-PAGE, and functional validation prior to release. A Certificate of Analysis (CoA) and Safety Data Sheet (SDS) are available on request.

Nuclease activity typically requires divalent metal ion cofactors (Mg²⁺ or Mn²⁺ at 1–5 mM). Activity is inhibited by chelating agents such as EDTA (≥1 mM), high salt concentrations, and reducing agents such as DTT at elevated concentrations. Heat inactivation (65–75°C for 15 min) is effective for most nucleases, allowing removal of enzyme activity after digestion without column purification.

Yeasen Biotechnology supports custom enzyme solutions across multiple service lines — from GMP-grade bulk supply to directed enzyme engineering. Contact BioHippo to discuss requirements and initiate a project inquiry.

▶ GMP-Grade & Bulk Supply

Select Yeasen enzymes are available in GMP grade, manufactured in an ISO 13485-certified UCF.ME™ ultra-clean molecular enzyme facility with FDA Drug Master File (DMF) support.

  • GMP-grade release testing and CoA documentation
  • ISO 13485-certified production facility
  • Scalable from milligram to multi-gram quantities
  • Consistent lot-to-lot activity specifications

▶ Glycerol-Free & Custom Formulation

Glycerol-free enzyme formats are available for applications requiring lyophilization compatibility, liquid handling automation, or direct IVD master mix integration.

  • Glycerol-free liquid format (standard and custom buffers)
  • Lyophilization-ready enzyme preparation
  • Custom reaction buffer optimization for specific assay conditions
  • Compatible with freeze-drying workflows for point-of-care formats

▶ Molecular IVD RDC Service

Yeasen's Research and Development Contracting (RDC) team delivers end-to-end solutions for molecular diagnostic product development, covering enzyme selection through clinical validation support.

  • Enzyme selection and performance matching
  • Primer/probe design and reaction buffer optimization
  • Sensitivity, specificity, and precision validation studies
  • Stability studies and SNP evaluation
  • Instrument platform compatibility assessment

▶ ZymeEditor™ Enzyme Engineering

Yeasen's proprietary ZymeEditor™ directed evolution and rational design platform enables the development of custom enzyme variants with tailored performance characteristics not available in off-the-shelf products.

  • Directed evolution for enhanced thermostability, processivity, or fidelity
  • Rational design for altered substrate specificity or cofactor requirements
  • Library screening from Yeasen's proprietary enzyme variant collection
  • Scale-up to commercial quantities upon candidate confirmation

ⓘ Customization services are fulfilled by Yeasen Biotechnology. Lead times and minimum order quantities vary by service type. Contact BioHippo for project scoping and pricing.

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