Zeigt alle 5 Ergebnisse
-
not rated 31,00 € – 379,00 €Taq DNA Polymerase, recombinant
Taq DNA Polymerase is now supplied with -inhibitor free- DNA Loading buffer IF
- Best choice for colony PCR
- Adds a single deoxyadenosine (A) to the 3′- ends of PCR products
- No detectable 3’→5′ proofreading exonuclease activity
- For standard PCR where proofreading is not required
- Excellent cost-performance ratio
Concentration: 5U/µL
Source: Purified from an E. coli strain carrying a plasmid with Taq DNA polymerase gene from Thermus aquaticus YT-1.
Reagents supplied with: 10x Taq polymerase buffer and 10x DNA Loading buffer IF -inhibitor free-
Store at: -20 °C -
not rated 109,50 €PCR Cooler „Gold“ 96+6 Aluminium | Kühlständer für 96 Well PCR Platten
• Lead free aluminum alloy
• Excellent heat transfer
• Suitable for 96 well PCR plates, 8 well PCR strips and 0.2 mL PCR single tubes
• 6 additional milled holes for 1.5 mL tubes
• Even temperature distribution
• For cooling on ice
• Autoclavable at 121 °C
• Conical milling, straight top for perfect fit
• Anodized in gold color
• 2 years warranty
• Made in Germany -
not rated 1.849,00 € – 3.290,00 €PCR Workstation | PCR Cabinet | PCR Workbench | UV PCR Bench
PCR Workstatation L • Designed and produced in Germany
• Effective DNA/RNA inactivation with powerful high intensity UV tube
• Prevents your samples from cross contamination
• Adjustable timer
• Total operating time counter for UV tubes
• Easy change of the UV tubes
• Two integrated power outlets for lab equipment
• Economic, energy saving and silent
• Custom sizes available on request -
not rated 4.639,00 €Thermocycler 96 Well PCR- GTC96S Cleaver Thermal Cycler
The Cleaver Scientific GTC96S Thermal Cycler is compatible with all standard 96 plates and 0.2 ml PCR tubes. The wells for the tubes can be divided into six discrete (4×4 well) temperature zones, easily distinguished by blue and black squares. … Read More -
not rated 42,10 € – 169,50 €Klenow Enzyme (DNA Polymerase I Large Fragment)
Concentration: 5U/µL
• Highly pure recombinat enzyme (>98 % as indicated by SDS-PAGE)
• Lacks the 5´->3´ exonuclease activity
• Retains polymerase and 3’→5’exonuclease activity (proofreading, blunting)
• Fill-in of 5’ overhangs to form blunt ends (blunting)
• Second strand cDNA synthesis
• Probe labelling, using random primersSource: E. coli strain carrying a plasmid with a clone copy of DNA Polymerase I large fragment
Reagents supplied with: 10x Klenow reaction buffer
Store at: -20 °C
