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P4390

Polynukleotid-Kinase aus T4-infizierten E. coli

10 units/μL, buffered aqueous glycerol solution

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Ihnen/SKUVerfügbarkeitPreis
100 units
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€ 151,00
500 units
Warenkorb auf Verfügbarkeit prüfen
€ 607,00

Über diesen Artikel

CAS-Nummer:
UNSPSC Code:
12352204
NACRES:
NA.53
EG-Nummer:
MDL number:
Concentration:
10 units/μL

€ 151,00


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grade

Molecular Biology

Quality Segment

form

buffered aqueous glycerol solution

mol wt

33 kDa

concentration

10 units/μL

foreign activity

Endonuclease and exonuclease, none detected

shipped in

wet ice

storage temp.

−20°C

Application

Suitable for:
  • Sequencing or nucleic acid tagging (DNA and RNA) by 5′-end labeling
  • 5′ phosphorylation of oligonucleotides
  • Removal of 3′-phosphate groups from phosphorylpolynucleotides

Biochem/physiol Actions

Polynucleotide kinase catalyses a "forward reaction" transfer of the γ-phosphate of ATP to the 5′ hydroxyl terminus of single- and double-stranded nucleic acids (DNA and RNA) and 3′-nucleoside monophosphates. In exchange reactions containing ADP, the enzyme will catalyze the exchange of 5′-terminal phosphate groups and ATP. The 3′-phosphatase activity enables the enzyme to remove 3′-phosphoryl groups from phosphorylpolynucleotides.
1. Forward reaction: Transfer of the labeled γ-phosphate from [γ-32P]-ATP to the free 5′-hydroxyl group of the substrate.
5′-HO-DNA + [γ-32P]-ATP → 5′-32PO-DNA + ADP.
Substrates that do not have a free 5′-hydroxyl require prior dephosphorylation by alkaline phosphatase.
2. Exchange reaction: First, the terminal 5′-phosphate is transferred from the substrate to ADP present in the reaction mixture. Then, the labeled γ-phosphate from [γ-32P]-ATP is transferred to the free hydroxyl group of the substrate.
5′-PO-DNA + ADP → 5′-HO-DNA + ATP
5′-HO-DNA + [γ-32P]-ATP → 5′-32PO-DNA + ADP

Analysis Note

Activity is determined in a reaction mixture containing 40 mM Tris-HCl (pH 7.5), with 10 mM MgCl2, 5 mM dithiothreitol, 0.5 mM 5′-OH polynucleotide ends, and mM [γ-32P]-ATP.

Other Notes

One unit catalyzes the transfer of one nanomole of 32P to the 5′-end of micrococcal nuclease-treated DNA in 30 min. at 37 °C. Transfer is detected as incorporation into acid-insoluble material.
T4 Polynucleotide Kinase is supplied in a solution of 50% glycerol (v/v), 20 mM Tris-HCl (pH 7.5), 25 mM KCl, 2mM DTT, 0.1 mM EDTA, and 0.1 μM ATP.

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Dieser Artikel
SRE0005D8276P4850
grade

Molecular Biology

grade

Molecular Biology

grade

Molecular Biology

grade

Molecular Biology

form

buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

form

buffered aqueous glycerol solution

concentration

10 units/μL

concentration

≥10 mg/mL protein, ≥800 unit/mL

concentration

~3,000 units/mL

concentration

≥10 mg/mL, ≥800 units/mL

mol wt

33 kDa

mol wt

28.93 kDa

mol wt

103 kDa

mol wt

28.93 kDa

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

-

storage temp.

−20°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C


pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Resp. Sens. 1

Lagerklasse

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)



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Questions

  1. Does "Polynucleotide Kinase from T4-infected Escherichia coli" is provided with buffer. what is composition of buffer.

    1 answer
    1. The product is supplied in a solution of 50% (v/v) glycerol, 20 mM Tris-HCl, pH 7.5, with 25 mM KCl, 2 mM DTT, 0.1 mM EDTA, and 0.1 uM ATP.

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