Uracil-DNA Glycosylase
Uracil-DNA Glycosylase (UDG) prevents carry over of DNA in PCR reactions
| Cat.-no |
Description |
Amount |
Price € |
Shop |
| 111-005 |
Uracil-DNA Glycosylase (UDG) HC |
200 units |
40.00 |
add |
| 111-025 |
Uracil-DNA Glycosylase (UDG) HC |
1000 units |
150.00 |
add |
Uracil-DNA Glycosylase (UDG): Request/order by e-mail HC=high concentrated
Uracil-DNA Glycosylase (UDG): Datasheet
Uracil-DNA Glycosylase (UDG): Deutsche Beschreibung
Applications:
- site-directed mutagenesis
- as a probe for protein-DNA interaction studies
- Glycosylase mediated single nucleotide polymorphism detection (GMPD)
- SNP genotyping
- Rapid and efficient cloning of PCR products
- Elimination carry-over contamination in PCR
Description:
The Uracil-DNA Glycosylase (UDG, UNG) catalyzes the hydrolysis of the N-glycosylic bond between the uracil and sugar, leaving an apyrimidinic site in uracil-containing single or double-stranded DNA. Shows no activity on RNA. Molecular weight: 25.6 kDa monomer.
Concentration:
high concentrated HC: 20 - 40 u/µl
Storage Buffer:
20 mM Tris-HCl (pH 8.0); 50 mM NaCl; 1 mM EDTA; 7 mM 2-mercaptoethanol; 50% glycerol
Reaction Buffer 10X
200 mM Tris-HCl (pH 8.0 at 25°C), 10 mM EDTA, 10 mM DTT. Incubation of 1X buffer at 37°C.
Unit definition:
One unit is defined as the amount of enzyme that catalyzes the release of 60 pmol of uracil per minute from double-stranded, uracil-containing DNA. Activity is measured by release of [3H]-uracil in a 50 µl reaction containing 0,2 µg DNA (104 – 105 cpm/µg) in 30 minutes at 37°C.
Quality control:
Free of endodeoxyribonucleases, exodeoxyribonucleases, phosphatases and ribonucleases.
Usage:
Treatment of 1 µg of uracil-containing DNA with 1 unit of UDG for 10 minutes at 37°C renders the DNA incapable of being copied by DNA polymerase. 95 % of the enzyme can be inactivated by incubation at 95°C for 10 minutes.
Transportation: on blue ice
Storage: at -20°C for 24 months
Related products:
>>> Service pages in English <<<
>>> Serviceseiten auf Deutsch <<<
Copyright© GeneOn 2007-10 |

|
