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T4PNK-RO

Roche

T4 Polynucleotide Kinase, 3′-phosphatase free

from phage T4 am N81 pse T1 infected Escherichia coli BB

Synonym(s):

kinase, t4 polynucleotide, 3′-phosphatase-free

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About This Item

UNSPSC Code:
12352200

form

solution

specific activity

≥40 x 103 units/mg protein
40000 U/mg

packaging

pkg of 1,000 U (10838292001)
pkg of 200 U (10709557001)

manufacturer/tradename

Roche

storage temp.

−20°C

General description

T4 polynucleotide kinase catalyzes the transfer of the terminal phosphate group of ATP to the 5′-hydroxyl terminus of DNA or RNA. It also can catalyze the exchange of 5′-terminal phosphate groups. In contrast to the wild type E. coli enzyme, this phage derivative lacks 3′-phosphatase activity. The assay time is 30 minutes and volume activity is 10000 U/ml.

Application

Use T4 Polynucleotide Kinase, 3′-phosphatase-free, to:
  • Phosphorylate the 5′ ends of RNA or DNA
  • Phosphorylate the 3′ ends of RNA to prevent cyclization
  • Add a 5′[32P]-terminal label to 3′-CMP, forming 5′[32P]pCp. This substrate is commonly used for 3′-end labeling of RNA with T4 RNA ligase.
  • Label 5′-hydroxyl ends of DNA with [?-32P]-ATP (either by direct phosphorylation or by phosphate exchange)
  • Phosphorylate the 5′-hydroxyl ends of oligonucleotides obtained from automated synthesizers
  • Phosphorylate the 5′-hydroxyl ends of linkers.
  • Purify recombinant RNA in E. coli.

Note: The 3′-phosphatase activity of the wild-type kinase is not observed under optimal incubation conditions with the mutant T4 Polynucleotide Kinase.

Biochem/physiol Actions

T4 polynucleotide kinase catalyzes the transfer of the terminal phosphate group of ATP to the 5′-hydroxyl terminus of DNA or RNA. It also can catalyze the exchange of 5′-terminal phosphate groups. In contrast to the wild type E. coli enzyme, this phage derivative lacks 3′-phosphatase activity. The assay time is 30 minutes and volume activity is 10000 U/ml.

Packaging

1 kit containing 2 components

Quality

Absence of 3′-phosphatase, endonucleases, nicking activity, 3′-exonucleases, and ribonucleases, tested according to the current Quality Control procedures; function tested using the DNA 5′-End Labeling Kit.

Unit Definition

One unit is the enzyme activity which catalyzes the incorporation of 1 nmol 32P into acid-precipitable products within 30 minutes at +37 °C.

Volume Activity: 10 x 103 U/ml

Other Notes

For life science research only. Not for use in diagnostic procedures.

Kit Components Only

Product No.
Description

  • Enzyme Solution, in buffer, pH 7.5 (+25 °C) 10 U/μl

  • Phosphorylation Buffer 10x concentrated

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_c

does not flash


Certificates of Analysis (COA)

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Phosphorylating DNA with DNA
Li Y and Breaker RR
Proceedings of the National Academy of Sciences of the USA, 2746-51 null
Luc Ponchon et al.
Nature protocols, 4(6), 947-959 (2009-05-30)
RNA production using in vivo transcription by Escherichia coli allows preparation of milligram quantities of RNA for biochemical, biophysical and structural investigations. We describe here a generic protocol for the overproduction and purification of recombinant RNA using liquid chromatography. The

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