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The concentrated formulation does not contain glycerol and is suitable for the preparation of dry amplification mix preparations.", "Country": "XG", "Code": "Product Description", "Name": "Product Description" }, { "Language": "en", "Value": "Apply AptaTaq DNA Polymerase for:

• Fast PCR assays with no extra enzyme activation time and fast cycling protocols
• Single- or multiplex PCR and qPCR applications requiring high specificity, sensitivity, and yield
• RT-PCR
• Difficult templates with secondary structures or GC-rich sequences
• Formulation of dried-down amplification reagents

", "Country": "XG", "Code": "Applications", "Name": "Applications" }, { "Language": "en", "Value": "Will be supplied as \"AptaTaq DNA Polymerase, Glyc.-free, 50 U/uL\". Unit of measure is \"kU\".", "Country": "XG", "Code": "CB - Order Information", "Name": "CB - Order Information" }, { "Language": "en", "Value": "Reversible hot start Taq DNA Polymerase without initial activation step for maximum stability combined with sensitivity and specificity; lyo ready formulation for preparation of dried amplification mixes.", "Country": "XG", "Code": "Positioning", "Name": "Positioning" }, { "Language": "en", "Value": "The aptamer/polymerase mixture is a hot start system with reversible inhibition of the polymerase activity at lower temperatures. Polymerase inactivation is achieved by a tight bond of the folded aptamer-oligonucleotide to the active site of the polymerase at lower temperatures. Upon heating above +60°C, the aptamer acts like a molecular switch, changing its temperature-dependent tertiary structure and releasing the active polymerase. Dropping the temperature below +55°C shuts off the polymerase activity again. Similar to antibody-based methods, the enzyme is much more quickly activated by heating, than chemically modified polymerases. In contrast to antibodies, the aptamer-oligonucleotide is much more stable, allowing longer storage at room temperature.", "Country": "XG", "Code": "Background Information", "Name": "Background Information" }, { "Language": "en", "Value": "

• Reduce time to result.
  Save up to 15 minutes per run by omitting the initial activation step required by chemically modified hot start polymerases, and reduce cycling time with fast protocols.
• Maximize specificity, sensitivity, and yield.
  Achieve reliable amplification of your target DNA from various sources (e.g., genomic DNA, cDNA, plasmids).
• Simplify PCR setup.
  Store these highly stable polymerase for up to 1 month at +2° to +8°C and setup your hot start PCR reaction at room temperature.
• Obtain consistent results.
  Roche standardized manufacturing processes include extensive Quality Control release testing for high lot-to-lot consistency ideal for (IVD) kit manufacturers and end users.
• Prepare stable amplification mixes in dry format.
  Use this formulation for producing dried-down amplification mixes stable at room temperature.

", "Country": "XG", "Code": "Benefits", "Name": "Benefits" }, { "Language": "en", "Value": "Appearance: Clear, colorless solution
Storage buffer: Tris/HCl, 20 mmol/L; KCl, 100 mmol/L; EDTA, 0.1 mmol/L; DTT, 1 mmol/L; Nonidet P40, 0.5% (v/v); Tween 20, 0.5% (v/v); pH approximately 8.0 at +4°C
Volume activity: 55±5 U/μL
Glycerol content: ≤0.1% (v/v)
Aptamer concentration (HPLC): 35.75 μmol/L ±10%
Unspecific endonucleases (λDNA): Not detectable in up to 30 U after 16 hours incubation at +37°C.
Nicking activity (pBR322 DNA): Not detectable in up to 30 U after 16 hours incubation at +37°C.
Exonucleases (³H-DNA): Not detectable in up to 30 U after 4 hours incubation at +65°C.
Performance test in qPCR using LightCycler^® 480 (≥0.03 ng human genomic DNA, 339 bp tPA fragment): Corresponds to reference
Stability: At -15 to -25°C within specification range for 24 months.", "Country": "XG", "Code": "Specification", "Name": "Specification" }, { "Language": "en", "Value": "AptaTaq DNA Polymerase is active at temperature above +60 to +65°C and inactive below +55°C. This hot start feature eliminates the risk of nonspecific primer extension. Taq DNA Polymerase is a highly processive 5'-3' DNA Polymerase that lacks 3'-5' exonuclease activity. Taq DNA Polymerase is stable during prolonged incubations at elevated temperatures (+95°C). The enzyme exhibits highest activity at a pH of approximately 9 (adjusted at +20°C) and temperatures approximately +75°C. The inherent stability of Taq DNA Polymerase is shown by the high storage stability in refrigerator and freezer (24 months at +2 to +8°C and -25 to -25°C). Taq DNA Polymerase accepts dNTP analogs as substrates.
pH optimum: Approximately 9.0 (+20°C)
Temperature optimum for elongation: Approximately +75°C
Half life at +95°C: Approximately 40 minutes
Divalent ion requirement: Mg²⁺ (standard concentration, 1.5 mmol/L)
dNTP requirement: Approximately 200 μmol/L for each dNTP", "Country": "XG", "Code": "Properties", "Name": "Properties" } ] } } ] }