Polynucleotide Kinase T4

2,500.00 10,000.00 

  • CNY: 191.40 ¥ - 765.60 ¥

  • Источник: Выделена из штамма E.coli, содержащего клонированный ген полинуклеитидкиназы из бактериофага Т4
  • Оптимальный буфер: SE-буфер полинуклеотидкиназа T4
  • Оптимальная температура: 37
SKU: SE-E311 Category:

Available Options

SKUРackagePackageConcentrationPrice 
E311S500 u10 000 u/ml2,500.00 
  • CNY: 191.40 ¥
E312L2500 u10 000 u/ml10,000.00 
  • CNY: 765.60 ¥

Description

T4 polynucleotide Kinase 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. The enzyme also catalyzes the removal of 3` – phosphoryl groups from 3` – phosphoril polynucleotides, deoxynucleoside 3` – monophosphates and deoxynucleoside 3` – diphosphates.
Applications:
– end-labeling DNA or RNA for probes and DNA sequencing;
– addition of 5` – phosphates to oligonucleotides to allow subsequent ligation;
– removal of 3` – phosphoril groups.

Source: Isolated from E.coli strain that carries the cloned Polynucleotide kinase gene from bacteriophage T4

Unit definition: T4 polynucleotide Kinase 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. The enzyme also catalyzes the removal of 3` – phosphoryl groups from 3` – phosphoril polynucleotides, deoxynucleoside 3` – monophosphates and deoxynucleoside 3` – diphosphates.
Applications:
– end-labeling DNA or RNA for probes and DNA sequencing;
– addition of 5` – phosphates to oligonucleotides to allow subsequent ligation;
– removal of 3` – phosphoril groups.

Reaction buffer: SE-buffer polynucleotide kinase T4

Storage conditions: 10 mM Tris-HCl (pH 7.5); 50 mM NaCl; 0.1 mM EDTA; 1 mM DTT; 50% glycerol; Store at -20°C.

Quality control: The enzyme is purified free of contaminating endonucleases, exonucleases, phosphatases.