Store at -20°C, avoid frequent thawing and freezing

Taq Pol (5 units/µl)
10x Taq Reaction Buffer complete
10x Taq Reaction Buffer without MgCl₂
MgCl₂ Stock Solution

Taq Pol is recommended for use in routine PCR reactions. It is optimized for high specificity and guarantees minimal by-product formation. The buffer system is recommended for plate based PCR and automated pipetting.
The enzyme replicates DNA at 72°C. It catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exo-nuclease replacement activity but lacks a 3'→5' exonuclease activity.
Taq Pol - red contains an inert red dye for easier handling and to facilitate the preparation of the master mix.

Store at -20°C, avoid frequent thawing and freezing

Taq Pol (5 units/µl)
10x High Yield Buffer complete
10x High Yield Buffer without MgCl₂
MgCl₂ Stock Solution

Taq Pol / high yield is recommended for use in routine PCR reactions. The buffer system is optimized for high efficiency and gives superior amplification results in a broad range of reaction conditions with most primer-template pairs. The buffer system facilitates the incorporation of labeled or modified nucleotides into DNA. Note that the ammonium based buffer contains detergents and may interfere with automated pipetting systems.
The enzyme replicates DNA at 72°C. It catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exo-nuclease replacement activity but lacks a 3'→5' exonuclease activity.
Taq Pol - red / high yield buffer contains an inert red dye for easier handling and to facilitate the preparation of the master mix.

Store at -20°C, avoid frequent thawing and freezing

Hot Start Pol (5 units/µl)
10x Hot Start Buffer complete
10x Hot Start Buffer without MgCl₂
MgCl₂ Stock Solution

Hot Start Pol provides improved specificity and sensitivity when amplifying low-copy-number targets in complex backgrounds or when prolonged room-temperature set up is required. The polymerase activity is blocked at ambient temperature and switched on automatically at the onset of the initial denaturation. The thermal activation prevents the extension of nonspecifically annealed primers and primer-dimer formation at low temperatures during PCR setup.
The enzyme catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exonuclease replacement activity but lacks a 3'→5' exonuclease activity.
Hot Start Pol requires no prolonged activation step. The polymerase inhibiting ligand is quickly released at the increased temperature of thermal cycling.
Hot Start Pol - red contains an inert red dye for easier handling and to facilitate the preparation of the master mix.

Store at -20°C, avoid frequent thawing and freezing

Rapid Pol
Rapid Buffer
MgCl₂ Stock Solution

Rapid Pol Rapid Pol is based on a specifically processed enzyme engineered for higher processivity and speed, offering significantly faster extension rates than wild-type Taq polymerase.
The rapid polymerase is designed for Fast PCR, in which total reaction times are 20-70% shorter compared with conventional PCR assays. This can be achieved without sacrificing reaction performance or the requirement for specialized PCR consumables or thermocyclers.

Store at -20°C, avoid frequent thawing and freezing

High Fidelity Pol (2.5 units/µl)
10x High Fidelity Buffer

High Fidelity Pol is based on a blend of Taq DNA polymerase and a proofreading enzyme specially designed for highly accurate and efficient amplification. It shows excellent results with extremely long (up to 30 kb), GC-rich or other difficult templates.
The enzyme blend includes a highly processive 5'→3' DNA polymerase and possesses a 5'→3' polymerization-dependent exonuclease replacement activity. Its inherent 3'→5' exonuclease proofreading activity results in a greatly increased fidelity of DNA synthesis compared to Taq polymerase.
The enzyme is highly purified and free of bacterial DNA.

Store at -20°C, avoid frequent thawing and freezing

High Fidelity Hot Start Pol (2.5 units/µl)
10x High Fidelity Buffer

High Fidelity Hot Start Pol is based on a blend of Taq DNA polymerase and a proofreading enzyme specially designed for highly accurate and efficient amplification. The additional hot-start function provides improved specificity and sensitivity when amplifying low-copy-number targets in complex backgrounds or when prolonged room-temperature set up is required. The polymerase activity is blocked at ambient temperature and switched on automatically at the onset of the initial denaturation. The thermal activation prevents the extension of nonspecifically annealed primers and primer-dimer formation at low temperatures during PCR setup.
The enzyme shows excellent results with extremely long (up to 30 kb), GC-rich or other difficult templates.
Activation step
High Fidelity Hot Start Pol requires no prolonged heating or denaturing step. The polymerase inhibiting antibodies are released at the increased temperature of the initial denaturation.

Store at -20°C, avoid frequent thawing and freezing

Pfu-X Polymerase (2.5 units/µl)
Pfu-X Buffer (10x conc.)

Pfu-X Polymerase is the ideal choice for applications where the efficient amplification of DNA with highest fidelity is required.
The enzyme is a genetically engineered Pfu DNA polymerase, but showing a 2-fold higher accuracy and an increased processivity, resulting in shorter elongation times.
The enzyme catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction but does not possess a 5'→3' exonuclease replacement activity. Its inherent 3'→5' exonuclease proofreading activity results in a greatly increased fidelity of DNA synthesis compared to Taq polymerase. Pfu-X Polymerase-generated PCR fragments are blunt-ended.
The enzyme is highly purified and free of bacterial DNA.

Store at -20°C, avoid frequent thawing and freezing

Sequencing Pol (5 unis/µl)
10x Sequencing Buffer without MgCl₂
MgCl₂ Stock Solution

Sequencing Pol is a Taq polymerase mutant showing an enhanced efficiency for incorporation of ddNTPs. Its capability of incorporating ddNTPs and dNTPs at equal rates makes it the ideal choice for DNA cycle sequencing.
The enzyme replicates DNA at 74°C. It catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium and has a 5'→3' polymerisation-dependent exonuclease replacement activity only.