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LDx, Glyc.-free, 50 U/μL\". Unit of measure is \"kU\".", "Name": "CB - Order Information" }, { "Language": "en", "Value": "Select AptaTaq DNA Polymerase LDx to perform microbial testing and other assays where the absence of contaminating bacterial, fungal, and/or human DNA is crucial. AptaTaq DNA LDx Polymerase is ideal for:
  • Fast PCR assays with no extra enzyme activation time and fast cycling protocols
  • Single- and multiplex PCR and qPCR applications that require high specificity, sensitivity, and yield
  • RT-PCR
  • Difficult templates with complex secondary structures or GC-rich sequences
  • Formulation of dried-down amplification reagents
", "Name": "Applications" }, { "Language": "en", "Value": "AptaTaq DNA Polymerase LDx is a blend of Taq DNA Polymerase and a specific oligonucleotide (aptamer) with hot start features, optimized for applications detecting the lowest levels of DNA.", "Name": "Product Description" }, { "Language": "en", "Value": "
  • Minimize risk of contaminating nucleic acids.
    AptaTaq DNA Polymerase LDx is extensively evaluated using ultra sensitive tests for detecting contaminating nucleic acids from bacteria and fungi. Roche has developed a nucleic acid-free workflow with clearly defined, highly consistent manufacturing processes resulting in a product with very low nucleic acid background.
  • Prepare stable amplification mixes in dry format.Use this formulation for producing dried-down amplification mixes stable at room temperature.
  • Enjoy the benefits of the advanced AptaTaq hot start system.
    Refer to AptaTaq DNA Polymerase for additional benefits like speed, easy handling and consistent results.
", "Name": "Benefits" }, { "Language": "en", "Value": "Reversible hot start Taq DNA Polymerase without initial activation step for maximum stability combined with sensitivity and specificity in microbial testing; lyo ready formulation for preparation of dried amplification mixes.", "Name": "Positioning" }, { "Language": "en", "Value": "LDx quality contains a very low DNA background, as verified using an ultra-sensitive LightCycler® assay for the absence of gram(+), gram(-) bacteria, and fungal DNA. To pass this Quality Control test, the level of contaminating nucleic acid must be <1 genome equivalent per 20 units of DNA polymerase. Furthermore, it is analyzed for the absence of contaminating human DNA with a LightCycler® test, specific for β-globin.", "Name": "Quality Control" }, { "Language": "en", "Value": "For information on LDx refer to AptaTaq DNA Polymerase LDx, 5 U/μl
For additional information on the AptaTaq hot start system, see AptaTaq DNA Polymerase, 5 U/μl", "Name": "Background Information" }, { "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.
Tests for the presence of contaminating nucleic acids
(human genomic DNA, β-Globin fragment): Corresponds to specification
(LC UniTool Resolight assay, specific for grampositive and gramnegative bacterial DNA and fungi DNA, <1.0 copy genomic DNA/20 U enzyme): Corresponds to specification
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 12 months.", "Name": "Specification" }, { "Language": "en", "Value": "AptaTaq DNA Polymerase LDx 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 lacking 3'-5' exonuclease activity. Taq DNA Polymerase is stable during prolonged incubations at elevated temperatures (+95°C). This enzyme exhibits highest activity at a pH of approximately 9 (adjusted at +20°C) and temperatures approximately +75°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", "Name": "Properties" } ] } } ] }

AptaTaq DNA Polymerase LDx, 50 U/μl

from Thermus aquaticus BM, expressed in E. coli, glycerol-free solution

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