x

DTI UNG 25 U/µl - Glycerol Free

DTI Uracil DNA Glycosylase(UNG), Heat-labile, (Glycerol Free) (25 U/ μl) hydrolyzes N-glycosylic bonds between the deoxyribose sugars and the uracil bases in uracil-containing DNA leaving apyrimidinic sites in the DNA. UNG excises uracil from both single- and double-stranded dU-containing DNA but not from RNA. The high concentration glycerol free version makes the product suitable for lyophilisation.

Brand Catalogue Number Pack Size
DTI UNG 25 U/µl – Glycerol Free
DT0106.250
250 U
DTI UNG 25 U/µl - Glycerol Free
Components
Component Pack Size
DTI Uracil DNA Glycosylase (UNG), Heat-labile, (Glycerol Free) (25 U/μl)
10 µl
Customized Pack Size
Available upon request
Storage Buffer
Component Concentration
Tris-HCl, pH 8.0 (at 4℃)
20 mM
KCl
100 mM
DTT
1 mM
EDTA
0.1 mM
NP-40
0.5% (v/v)
Tween 20
0.5% (v/v)

Storage and Shipment Conditions: -80°C

Source: Produced in E. coli strain expressing a recombinant Xiphophorus maculatus UNG mutant.

Unit Definition: One unit of UNG is defined as the amount of enzyme required to digest 1 μg of uracil-containing dsDNA at 25℃ in 30 min.

Application: Used in further manufacturing and lyophilization processes for PCR, RT-PCR, and LAMP assays.

Inactivation by Heat: The enzyme is completely and irreversibly inactivated by heat incubating at 50℃ for 10 min.

Usage Protocol

• Use as per the requirement. Can be diluted if needed.

• Add suitable enzyme amounts based on application (typically 0.1 – 1 U/50μl reaction volume).

• UNG activation: Incubate for 10 min at 25℃.

• UNG inactivation: Incubate for 2 min at 95℃.

• Follow the specific protocol for application.

Quality Control Data: Please refer to the certificate of analysis for each lot.

DTI UNG 25 U/µl - Glycerol Free - Protocol and Downloads
Document Download Link
DTI UNG 25 U/µl – Glycerol Free – Protocol
DTI UNG 25 U/µl – Glycerol Free – Certificate of Analysis
Experimental Sample - Performance Data

qPCR reactions was performed with two qPCR reaction mix: One with UNG at a concentration of 2 U/ μl and other without UNG. Both these mixes were spiked with dU-containing amplicons, mimicking carryover contamination. The reaction mix without UNG generated a regular amplification curve, while the reaction mix containing UNG degraded the dU-containing amplicons resulting in significant reduction in amplification from the mimicking carryover contamination.