11444646001
Roche
Uracil-DNA Glycosylase
recombinant from E. coli K 12
Synonym(s):
PCR, UDG
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About This Item
Recommended Products
recombinant
expressed in E. coli
Quality Level
form
solution
packaging
pkg of 100 U
manufacturer/tradename
Roche
concentration
1000 U/mL
technique(s)
PCR: suitable
mutagenesis: suitable
color
colorless
pH
7.9-8.1 (68 °F)
solubility
water: miscible
suitability
suitable for molecular biology
application(s)
life science and biopharma
foreign activity
RNases 10 units, none detected
endonuclease 20 units, none detected
storage temp.
−20°C
Related Categories
General description
Uracil-DNA Glycosylase (UNG) contains the highly active recombinant form of the equally named enzyme found in prokaryotes and eukaryotes. It hydrolyzes uracil-glycosidic bonds in single- or double-stranded DNA, excising uracil and creating alkali-sensitive abasic sites in the DNA. These abasic sites can be hydrolyzed by endonuclease, heat, or alkali treatment. Depending on how the DNA is prepared, Uracil-DNA Glycosylase can be used to achieve general, site-specific, or strand-specific U-DNA cleavage.
Specificity
- Uracil-DNA glycosylase hydrolyzes uracil-glycosidic bonds at U-DNA sites in single- and doublestranded DNA, excising uracil and creating alkali sensitive abasic sites in the DNA.
- The enzyme is more active on single-stranded DNA than on double-standed DNA.
- Activity was also observed on small U-DNA oligonucleotides and on dUMP (Duncan, unpublished observations).
- Uracil-DNA glycosylase is inactive on RNA and native, uracil-free DNA.
Heat inactivation: 95 °C for 10 min
Uracil-DNA glycosylase remains partially active (<10%) after an incubation period of 30 minutes at 95 °C.
Application
Uracil-DNA Glycosylase can be used to cleave DNA at any site where a deoxyuridylate residue has been incorporated. U-DNA can be prepared by in vitro methods like PCR. General, site-specific, or strand-specific cleavage can be achieved with uracil-DNA glycosylase, depending on how the U-DNA is prepared. Uracil-DNA Glycosylase can therefore help you to:
- Prevent carryover contamination in PCR
- Increase the efficiency of site-directed mutagenesis procedures
- Label oligonucleotide probes
Quality
Carryover prevention activity is assayed by adding approximately 105dU that contains templates prior to the amplification reaction. After UNG treatment, no amplification products could be detected. The enzyme does not contain any contaminating exo- or endonucleases and is tested for the absence of RNases.
Unit Definition
One unit is defined as the amount of Uracil-DNA Glycosylase necessary to completely degrade 1 μg purified single-stranded uracil containing DNA (bacteriophage M13, grown in E.coli CJ 236 dut-ung-) at +37 °C in 60 minutes.
One Lindahl unit is defined as the amount of enzyme necessary to release of 1 μmol uracil at +37 °C in 1 minute. One Lindahl unit is comparable to 520,000 U based on our unit definition.
Volume Activity: 1 U/μl
One Lindahl unit is defined as the amount of enzyme necessary to release of 1 μmol uracil at +37 °C in 1 minute. One Lindahl unit is comparable to 520,000 U based on our unit definition.
Volume Activity: 1 U/μl
Physical form
The enzyme is supplied as 1U/μl solution in storage buffer.
Storage and Stability
OK to freeze (after DNA synthesis)
Other Notes
For life science research only. Not for use in diagnostic procedures.
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point(F)
No data available
Flash Point(C)
No data available
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