Firepol (regular Taq DNA Polymerase) 500 U

Supplier
LabOmics Solis Biodyne
Cat. No
6100500
Pack size
500 units
Links
Data Sheet MSDS

Features

• enhanced stability at room temperature: no activity loss for up to 1 month at RT
• Shipped at RT with no activity loss: save on shipping costs
• highly processive, thermostable DNA polymerase: 5’→3’ polymerization-dependent exonuclease replacement activity but lacks 3’→ 5’ exonuclease activity.

FIREPol® is a highly processive, thermostable DNA polymerase. Due to its genetic modifications FIREPol® has an enhanced stability at room temperature with no activity loss for up to 1 month. The enzyme has 5’→3’ polymerization-dependent exonuclease replacement activity but lacks 3’→ 5’ exonuclease activity.

• Source: Purified from an E.coli strain that carries an overproducing plasmid containing a modified gene of Thermus aquaticus DNA Polymerase.
• Concentration: 5U/µL
• Unit definition: One unit is defined as the amount of enzyme required to catalyze the incorporation of 10 nmol of dNTPs into an acid-insoluble form in 30 minutes at 74ºC.
• Storage and Dilution buffer: 50% glycerol (v/v), 20 mM Tris-HCl pH 8.7 at 25ºC, 100 mM KCl, 0.1 mM EDTA and stabilizers.
• Quality control: The enzyme is free of nicking and priming activities, exonucleases and non-specific endonucleases. SDS/PAGE - 95 kD band, >98% pure. Activity and stability tested via thermo-cycling. The error rate per nucleotide per cycle is ~ 2.5 x 10-5; the accuracy is ~ 4 x 104. Estimated half life at 95ºC is 1.5 hours.
• Shipping and Storage conditions: Routine storage: -20ºC Shipping and temporary storage for up to 1 month at room temperature has no detrimental effects on the quality of FIREPol® DNA Polymerase.

• Mix Composition:

• FIREPol® DNA Polymerase
• 10 x Reaction buffer B (Mg2+ free)

0.8 M Tris-HCl, 0.2 M (NH4)2SO4, 0.2% w/v Tween-20

• 10 x Reaction buffer BD(Mg2+ and detergent free)

0.8 M Tris-HCl, 0.2 M (NH4)2SO4

• 25 mM MgCl2
• 10 x Solution S

Additive that facilitates amplification of difficult templates (e.g. GC-rich DNA templates). This solution should be used at a defined working concentration (1x, 2x or 3x solution). Solution S is NOT a reaction buffer and should be used ONLY IF non-specific amplifications occur.

• Suited for a wide range of PCR assays
• TA cloning