OmniTaq 3
€0.00
In stock
SKU
VN1800E
Catalog Number: VN1800E
Size: 125 µl (500~1000 x 25 µl rxns)
Other Size(s): 50 µl (200~400 x 25 µl rxns)
Datasheet
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Size: 125 µl (500~1000 x 25 µl rxns)
Other Size(s): 50 µl (200~400 x 25 µl rxns)
Datasheet
Request Information
Inhibition-resistant Taq Pols & Master Mixes
- Inhibition-Resistant Taq DNA Polymerases are obtained by molecular engineering through mutagenesis of DNA polymerase gene to render enzymes resistant to PCR inhibitors such as blood, plasma, serum, soil, plant, water, chocolate, cheese and milk.
- Proven applications include forensics, environmental testing, agriculture and clinical diagnostics.
- Up to 40% whole blood, plasma or serum are tolerated and varying amounts of soil, plant and inhibitory foods.
- Provides superior amplification, even on damaged or degraded DNA templates.
- DNA extraction is often unnecessary, saving time and enabling amplification from minute quantities of DNA.
- Can tolerate more PCR inhibitors when combining with PCR enhancers.
OmniTaq 3 DNA Polymerase is a new generation mutant of Taq polymerase that is resistant to inhibitory effects from higher concentrations of blood, soil, plants, and more. It remains functional in 40% whole blood in PCR, even without PCR enhancer, and in some concentrations of crude soil extracts where other commercial enzymes fail. However, the presence of a PCR enhancer cocktail can further improve its tolerance. It can directly amplify the target gene from various sample types without DNA purification prior to PCR. This enzyme can be used in real-time PCR with both DNA binding dyes, such as SYBR Green and Eva Green, and TaqMan assay which requires 5’-3’ exonuclease activity.
OmniTaq 3 LA version (Long & Accurate) is available, which allows for amplification of longer products with higher fidelity and accuracy. It is compatible with real-time PCR with DNA binding dyes, such as SYBR Green and Eva Green. However, it is recommended to use the non-LA version for TaqMan assays in real-time PCR.
- Thermostability – more thermostable than standard Taq DNA polymerase
- Efficient – novel buffer system maximizes efficiency of PCR amplification, increases yield of any PCR product
- Robust and Inhibition-resistant – reliable direct amplification from crude samples without DNA purification and with even the most challenging DNA targets, especially when combining with our powerful PCR enhancers
- Flexible – LA version is ideal for amplifying any target up to 30 kb from DNA extracted from human, animal and plant samples
- Inhibition-Resistant Taq DNA Polymerases are obtained by molecular engineering through mutagenesis of DNA polymerase gene to render enzymes resistant to PCR inhibitors such as blood, plasma, serum, soil, plant, water, chocolate, cheese and milk.
- Proven applications include forensics, environmental testing, agriculture and clinical diagnostics.
- Up to 40% whole blood, plasma or serum are tolerated and varying amounts of soil, plant and inhibitory foods.
- Provides superior amplification, even on damaged or degraded DNA templates.
- DNA extraction is often unnecessary, saving time and enabling amplification from minute quantities of DNA.
- Can tolerate more PCR inhibitors when combining with PCR enhancers.
OmniTaq 3 DNA Polymerase is a new generation mutant of Taq polymerase that is resistant to inhibitory effects from higher concentrations of blood, soil, plants, and more. It remains functional in 40% whole blood in PCR, even without PCR enhancer, and in some concentrations of crude soil extracts where other commercial enzymes fail. However, the presence of a PCR enhancer cocktail can further improve its tolerance. It can directly amplify the target gene from various sample types without DNA purification prior to PCR. This enzyme can be used in real-time PCR with both DNA binding dyes, such as SYBR Green and Eva Green, and TaqMan assay which requires 5’-3’ exonuclease activity.
OmniTaq 3 LA version (Long & Accurate) is available, which allows for amplification of longer products with higher fidelity and accuracy. It is compatible with real-time PCR with DNA binding dyes, such as SYBR Green and Eva Green. However, it is recommended to use the non-LA version for TaqMan assays in real-time PCR.
- Thermostability – more thermostable than standard Taq DNA polymerase
- Efficient – novel buffer system maximizes efficiency of PCR amplification, increases yield of any PCR product
- Robust and Inhibition-resistant – reliable direct amplification from crude samples without DNA purification and with even the most challenging DNA targets, especially when combining with our powerful PCR enhancers
- Flexible – LA version is ideal for amplifying any target up to 30 kb from DNA extracted from human, animal and plant samples
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