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
Recommended Products
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:
Note: The 3′-phosphatase activity of the wild-type kinase is not observed under optimal incubation conditions with the mutant T4 Polynucleotide Kinase.
- 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
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
Proceedings of the National Academy of Sciences of the USA, 2746-51 null
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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