Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : EMNT2018
| Cat. No. | EMNT2018 |
| Description | digestion conditions, the enzyme selectively cleaves DNA that contains the modified base on one or both strands. The consensus cleavage site of Pvu Rts1I is 5-hmCN11-12/N9-10G.2 Pvu Rts1I serves as a useful tool to analyze 5-hmC patterns within the genome. In addition to distinguishing between 5-mC and 5-hmC in ds DNA, the enzyme can also cleave both glucosylated and nonglucosylated 5-hmC ds DNA.The enzyme is available in a 100-unit size at a concentration of 1 U/μl. The enzyme is supplied with a 10X Reaction Buffer. |
| Concentration | 1000 units/ml |
| Applications | Differentiation of 5-hmC from 5-mC. Cleavage of DNA at glucosylated and nonglucosylated 5-hmC. |
| Size | 100 units |
| Unit Definition | One unit is the amount of Pvu Rts1I needed for complete digestion of 1 μg of T2 gt- DNA in 60 minutes at 30 °C in 1X Reaction Buffer, in a 50-μl reaction. |
| Storage | 50% glycerol containing 50 mM Tris-HCl (pH 7.5), 0.1 M NaCl, 0.1 mM EDTA, 1 mM DTT, and 0.1% Triton® X-100. |
A: Pvu Rts1I Endonuclease is for research use only and is not intended for any clinical applications.
A: Pvu Rts1I Endonuclease can cleave both glucosylated and non-glucosylated 5-hmC dsDNA.
A: The concentration of Pvu Rts1I Endonuclease is 1000 units/ml.
A: Pvu Rts1I Endonuclease is supplied with a 10X reaction buffer.
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