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. : EMDT0318
| Cat. No. | EMDT0318 |
| Description | Exclusively from CHIMERx, Human DNA Polymerase Beta is a repair enzyme used to fill gaps and nicks in double-stranded DNA |
| Applications | Repair polymerase able to synthesize DNA beyond the end of a gap or nick with simultaneous displacement of the non-replicated strand.Fills gaps and nicks. |
| Size | 100 Units;50 Units |
| Unit Definition | One unit is the amount of enzyme required to incorporate 1 pmole of total nucleotide into acid-insoluble form in 60 minutes at 37 °C under the stated assay conditions.. |
| Reaction Buffer | 50 mM Tris-HCl (pH 8.7).10 mM KCl.10 mM MgCl2.0.4 mg/ml bovine serum albumin.1.0 mM dithiothreitol.15% (v/v) glycerol.0.05 mM of each dCTP, dGTP, dTTP, and [α-32P]dATP.10 μg activated DNA.Reaction volume of 50 μl. |
| Reaction Conditions | Incubation at 37 °C |
| Storage | 20 mM Tris-HCl (pH 8.0)0.1 mM EDTA200 mM NaCl1 mM dithiothreitol50% (v/v) glycerol |
A: The enzyme activity of Human DNA Polymerase Beta is currently under testing, and we cannot guarantee it at the moment.
A: Human DNA Polymerase Beta is sourced from humans and is purified after expression in Escherichia coli.
A: It can be stored at -80°C for one year. To avoid repeated freeze-thaw cycles, it is recommended to aliquot and store upon receipt. After opening, it can be stored at -20°C for 3 months.
A: It should be noted that upon receipt, the product should be centrifuged before opening to prevent loss of freeze-dried powder.
A: You can use a solution or culture medium containing a certain concentration of carrier protein (e.g., 0.1% BSA, 5% HSA, 10% FBS, or 5% trehalose) to reconstitute the product. When serum-free experiments are required, you can replace it with a 5% trehalose solution as a carrier.
A: The ED50 value of recombinant protein products can vary with different batches or assay methods. It is recommended to determine the most suitable actual ED50 value for your experiments.
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