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Potvrzuji
  1. Úvodní strana
  2. Reagencie
  3. Life Technologies / Fermentas
  4. DNA/RNA modifying enzymes
  5. DNA/RNA Polymerases
  6. Properties of mesophilic DNA poymerases
  7. Klenow Fragment, exo–

Klenow Fragment, exo–

Kód produktu: EP0421 Kód výrobce: EP0421 Kód dodavatele: {31A38F76-D349-4425-8282-A235A4429EA7} Výrobce: Life Technologies Czech Republic s.r.o.
Klenow Fragment, exo–
2 577,30 Kč
2 130,00 Kč bez DPH
do týdne
300 Units

.

FastDigest buffer for 100% activity LO certified 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, exo- is the large fragment of DNA polymerase I. Exhibits 5'→3' polymerase activity, but lacks the 3'→5' and 5'→3' exonuclease activities.
Zobraz detailní popis

Detailní popis

Thermo Scientific Klenow Fragment, exo-, is the large fragment of DNA polymerase I . It exhibits 5'→3' polymerase activity, but lacks the 3'→5' and 5'→3' exonuclease activities of DNA Polymerase I. The 3'→5' exonuclease activity of the enzyme is eliminated by mutations in the 3'→5'-exonuclease active site ( see Reference1).

Highlights

  • Lacks 3'→5' exonuclease activity
  • Incorporates modified nucleotides (e.g., Cy3-, Cy5-, fluorescein-, rhodamine-, aminoallyl-, biotin-labeled nucleotides)
  • Active in restriction enzyme, PCR, and RT buffers

Applications

  • Random-primed DNA labeling ( see ​ References 2-4)
  • Labeling by fill-in 5'-overhangs of dsDNA
  • Strand displacement amplification (SDA) ( see ​ Reference 5)
  • DNA sequencing by the Sanger method ( see ​ Reference 6)

Note

Klenow Fragment, exo- is not recommended for DNA blunting reactions prior to DNA ligation since it frequently adds one or more extra nucleotides to the 3'-terminus of blunt-end DNA substrates in a  non-template directed fashion ( see ​ Reference8).

10X Reaction Buffer 500 mM Tris-HCl (pH8.0 at 25°C), 50mM MgCl 2 , 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 30min 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 MgCl 2 , 1mM 2-mercaptoethanol, 0.033mM dATP, 0.033mM dTTP, 0.4MBq/mL [  3 H]-dTTP, and 62.5µg/mL poly(dA-dT)·poly(dA-dT).
Hazardous No
Inactivation Inactivated by heating at 75°C for 10min or by the addition of EDTA.
Inhibition Inhibitors: metal chelators, PP i , P  i (at high concentrations) (  see Reference 7).
Molecular Weight 68kDa monomer.
Quality Control
  • The absence of endo- and exodeoxyribonucleases confirmed by appropriate quality tests.
  • Functionally tested in random-primed DNA labeling.
Source E. coli cells with a cloned DNA fragment of the mutated 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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