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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. T7 DNA Polymerase

T7 DNA Polymerase

Kód produktu: EP0081 Kód výrobce: EP0081 Kód dodavatele: {943549B4-5BA5-4D33-9597-53034C007970} Výrobce: Life Technologies Czech Republic s.r.o.
T7 DNA Polymerase
2 795,10 Kč
2 310,00 Kč bez DPH
do týdne
300 Units

.

B buffer for 100% activity FastDigest buffer for 100% activity G buffer for 100% activity 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
T7 DNA Polymerase, a template dependent DNA polymerase, catalyzes DNA synthesis in the 5'=>3' direction.

Zobraz detailní popis

Detailní popis

Thermo Scientific T7 DNA Polymerase, a template dependent DNA polymerase, catalyzes DNA synthesis in the 5'=>3' direction. It is a  highly processive DNA polymerase allowing continuous synthesis of long stretches of DNA. The enzyme also exhibits a high 3'=>5' exonuclease activity towards single- and double-stranded DNA.

Highlights

  • Strong 3’=>5’ exonuclease activity, approximately 1000-fold greater than Klenow Fragment (see Reference 1)
  • Active in restriction enzyme buffers

Applications

  • Purification of covalently closed circular DNA by removal of residual genomic DNA
  • Primer extension reactions on long templates (see​ Reference 1)
  • DNA 3'-end labeling (see​ Reference 1)
  • Strand extensions in site-directed mutagenesis (see​ Reference 2)
  • Fill-in blunting of 5'-overhang DNA
  • Second strand synthesis of cDNA (see​ Reference 3)
  • In situ detection of DNA fragmentation associated with apoptosis (see​ Reference 4)

Note

Assays at 37°C require only short incubation times (see​ Reference 6).

10X Reaction Buffer 400 mM Tris-HCl (pH 7.5 at 25°C), 100 mM MgCl2, 10 mM DTT.
CategoryName
Definition of Activity Unit
  • One unit of the enzyme catalyzes the incorporation of 10 nmol of deoxyribonucleotides into a polynucleotide fraction (adsorbed on DE-81) in 30 min at 37°C.
  • Enzyme activity is assayed in the following mixture: 40 mM Tris-HCl (pH 7.5), 10 mM MgCl2, 1 mM DTT, 0.1 mg/ml BSA, 0.33 mM of each dNTP, 0.4 MBq/ml [3H]-dTTP, and 0.5 mM alkali-denatured calf thymus DNA.
Hazardous No
Hazardous: No
Inactivation Inactivated by heating at 75°C for 10 min.
Inhibition Inhibitors: metal chelators, modification reagents (acetic anhydride, N-ethylmaleimide inactivate the 3'=>5' exonuclease activity but not the polymerase activity) (see Reference 5)
Molecular Weight The T7 DNA Polymerase is composed of two subunits: an 80 kDa polypeptide (the product of gene 5 of bacteriophage T7) and a 12 kDa thioredoxin (from the trxA gene of E. coli).
Quality Control The absence of endodeoxyribonucleases is confirmed by the appropriate quality test.
Shelf Life:
Shipping Condition:
Shipping Information
Source Two E. coli strains, one with the cloned gene 5 of bacteriophage T7, and the other with the cloned trxA gene of E. coli.
SpecificationName
SpecificationValue
Storage Buffer The enzyme is supplied in:
20 mM potassium phosphate (pH 7.4), 1 mM DTT, 0.1 mM EDTA and 50% (v/v) glycerol.
Storage Condition -20 C
Storage Condition:

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