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Klenow Fragment

Kód produktu: EP0052 Kód výrobce: EP0052 Kód dodavatele: {0416A9FE-0015-4BB7-B9D0-066724FD6F5E} Výrobce: Life Technologies Czech Republic s.r.o.
10 393,90 Kč
8 590,00 Kč bez DPH
do týdne
1500 units

.


FastDigest buffer for 100% activity Low concentration available O buffer for 100% activity Recombinant enzyme R buffer for 100% activity Tango buffer for 100% activity Thermal inactivation at 75°C in 10 min
Klenow Fragment is the Large Fragment of DNA Polymerase exhibiting 5'→3' polymerase, 3'→5' exonuclease (proofreading) activities, but lacking 5'→3' exonuclease activity.

Zobraz detailní popis

Detailní popis

Thermo Scientific Klenow Fragment is the large fragment of DNA polymerase I. It exhibits 5'→3' polymerase activity and 3'→5' exonuclease (proofreading) activity, but lacks 5'→3' exonuclease activity of DNA polymerase I.

Highlights

  • Incorporates modified nucleotides (e.g., Cy3-, Cy5-, aminoallyl-, biotin-, digoxigenin- and fluorescently-labeled nucleotides)
  • Active in restriction enzyme, PCR, RT, and T4 DNA Ligase buffers

Applications

  • DNA blunting by fill-in 5'-overhangs (see Reference 1)
  • Random-primed DNA labeling (see References 2-4)
  • Labeling by fill-in 5'-overhangs of dsDNA
  • DNA sequencing by the Sanger method
  • Reaction Buffer 500mM Tris-HCl (pH8.0 at 25°C), 50mM MgCl2, 10mM DTT.
    Definition of Activity
    • Unit One unit of the enzyme catalyzes the incorporation of 10nmol of deoxyribonucleotides into a polynucleotide fraction (adsorbed on DE-81) in 30minutes at 37°C, using poly(dA-dT)·poly(dA-dT) as a  template·primer.
    • Enzyme activity is assayed in the following mixture: 67mM potassium phosphate (pH7.4), 6.7mM MgCl2, 1mM 2-mercaptoethanol, 0.033mM dATP, 0.033mM dTTP, 0.4MBq/mL [3H]-dTTP, and 62.5µg/mL poly(dA-dT)·poly(dA-dT).
    Hazardous No
    Inactivation Inactivated by heating at 75°C for 10min or by addition of EDTA.
    Inhibition Inhibitors: metal chelators, PPi, Pi (at high concentrations) (see Reference 8).
    Molecular Weight 68kDa monomer.
    Quality Control
    • The absence of endodeoxyribonucleases confirmed by appropriate quality test.
    • Functionally tested for fill in of 5'-overhanging DNA termini and for random primed DNA labeling.
    Source E. coli cells with a cloned fragment of the polA gene.
    Storage Buffer The enzyme is supplied in: 25mM Tris-HCl (pH7.5), 0.1mM EDTA, 1mM DTT, and 50%(v/v) glycerol.
    Storage Condition -20 C

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