Uracil DNA Glycosylase (UDG/UNG), Heat-Labile (1 U/μL)
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Uracil DNA Glycosylase (UDG/UNG), Heat-Labile (1 U/μL)

Cat.No: IVDRM-0248 Datasheet

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Product Details Related Products
Product Name Uracil DNA Glycosylase (UDG/UNG), Heat-Labile (1 U/μL)
Catalog No. IVDRM-0248
Description Heat-labile Uracil DNA Glycosylase (UDG/UNG) catalyzes the hydrolysis of the N-glycosidic bond between the uracil base and the sugar-phosphate backbone of uracil-containing DNA, releasing free uracil. Compared with conventional UDG, this heat-labile enzyme avoids the degradation of dU-containing amplification products at room temperature caused by residual activity that may persist after inactivation of ordinary UDG. The enzyme works at room temperature, is temperature-sensitive and is easily inactivated.
Intended Use Prevention of carryover (aerosol) contamination from dU-containing PCR amplification products in dUTP-based PCR/qPCR systems
Removal of uracil bases from single-stranded or double-stranded DNA
Principle / Technology UDG excises uracil from DNA by hydrolyzing the N-glycosidic bond linking the uracil base to the deoxyribose-phosphate backbone, generating apyrimidinic (AP) sites. When PCR is performed with dUTP instead of dTTP, contaminating carryover amplicons from previous reactions are degraded by a UDG pre-treatment step, while the natural thymine-containing template remains unaffected.
Performance Range / Specifications Low nuclease background: free of exonuclease, nicking endonuclease and RNase contamination
Broad application: removes uracil bases from single-stranded or double-stranded DNA
Heat-labile: inactivated at 95 °C for 5-10 minutes
Compatible with RT-qPCR systems: no impact on the detection system even at high input (2 U per 20 uL reaction)
Specificity Specifically excises uracil bases from single-stranded and double-stranded DNA; does not act on natural thymine-containing DNA templates.
Reaction Conditions / Protocol Active at room temperature. A UDG pre-treatment step is performed before amplification in dUTP-based PCR/qPCR systems; the enzyme is then inactivated during the initial high-temperature step.
Storage Conditions Store at -25 °C to -15 °C.
Shelf Life 2 years when stored at -25 °C to -15 °C.
Package Specifications 100 U
500 U
10,000 U
100,000 U
500,000 U
Product Form Liquid
Quality Control Free of exonuclease, nicking endonuclease and RNase contamination.
Concentration 1 U/uL
Expiration Date / Stability Stable for 2 years at -25 °C to -15 °C.
Compatibility Compatible with RT-qPCR reaction systems; no impact on the detection system at high input (2 U per 20 uL reaction).
Application Notes / Precautions Unlike conventional UDG, this heat-labile enzyme eliminates the risk of residual activity degrading dU-containing amplification products at room temperature after the reaction. Use in dUTP-based amplification systems for carryover contamination control.
Recognition Site Uracil bases in single-stranded or double-stranded DNA (cleaves the N-glycosidic bond between uracil and the sugar-phosphate backbone)
Heat Inactivation 95 °C for 5-10 minutes

For research use only, not for clinical use.

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