Transfected Stable Cell Lines
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Cat. No. : EMQZ1405
| Cat. No. | EMQZ1405 |
| Description | Catalyzes the transfer and exchange of Pi from the γ position of ATP to the 5´ -hydroxyl terminus of polynucleotides (double-and single-stranded DNA and RNA) and nucleoside 3´-monophosphates. Polynucleotide Kinase also catalyzes the removal of 3´-phosphoryl groups from 3´-phosphoryl polynucleotides, deoxynucleoside 3´-monophosphates and deoxynucleoside 3´-diphosphates. |
| Source | A recombinant E. coli strain that carries the cloned T4 Polynucleotide Kinase gene. |
| Concentration | 10,000U/ml |
| Applications |
• End-labeling DNA or RNA for probes and DNA sequencing • Addition of 5´-phosphates to oligonucleotides to allow subsequent ligation • Removal of 3´-phosphoryl groups |
| Size | 200U; 1,000U |
| Unit Definition | One Richardson unit is defined as the amount of enzyme catalyzing the incorporation of 1 nmol of acid-insoluble [32P] in 30 minutes at 37°C. |
| Reaction Conditions | 1×T4 Polynucleotide Kinase Reaction System containing: 1×T4 Polynucleotide Kinase Reaction Buffer [70 mM Tris-HCl (pH 7.6 at 25°C),10 mM MgCl2,5 mM DTT]; incubate at 37°C. |
| Storage | Store at -20°C |
A: The concentration of this reagent is 10,000 U/ml.
A: Yes, catalyzes the transfer and exchange of Pi from the γ position of ATP to the 5´ -hydroxyl terminus of polynucleotides (double-and single-stranded DNA and RNA) and nucleoside 3´-monophosphates。
A: There are two reagents included in this product, Enzyme Solution and Phosphorylation Buffer 10x concentrated.
A: The reagent can be stored directly at -20℃.
A: The enzyme is expressed and purified from Escherichia coli, and its expression gene is derived from T4 bacteriophage.
A: Heating at 75℃ for 10 minutes can inactivate T4 Polynucleotide Kinase, and metal ion chelators, phosphates, ammonium ions, KCl and NaCl greater than 50mM can significantly inhibit the activity of T4 Polynucleotide Kinase.
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T4 Polynucleotide Kinase catalyzes the removal of 3´-phosphoryl groups from 3´-phosphoryl polynucleotides, deoxynucleoside 3´-monophosphates and deoxynucleoside 3´-diphosphates.
This reagent not only catalyzes 5'-hydroxyl terminal phosphorylation of polynucleotides, but also catalyzes phosphorylation of nucleoside 3'-monophosphates.
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