For further processing only. Others AptaTaq exo DNA Polymerase 50 U uL AptaTaq exo DNA Polymerase, 50 U/μl 3.6.17.2.1.10 from Thermus aquaticus BM, expressed in E. coli, glycerol-free solution 05364086103 AptaTaq delta exo DNA Pol., Glyc.-free AptaTaq exo DNA Polymerase, 50 U/uL 07613336130810 Reagents, kits custom fill 50 U/μL CustomBiotech product. Please contact your local representative. Will be supplied as "AptaTaq exo DNA Polymerase, Glyc.-free". Unit of measure is "kU". Use AptaTaq exo DNA Polymerase for: SNP analysis and genotyping Allele-specific PCR Multiplexing Arbitrarily primed PCR Formulation of dried-down amplification reagents When time to result matters, this novel hot start technology is ideal as it does not require any activation time. en AptaTaq DNA exo Polymerase is a blend of N-terminal truncated Taq DNA Polymerase and a specific oligonucleotide (aptamer) with hot start features, optimized for excellent discrimination against misextension. This concentrated formulation contains no glycerol and is suitable for the preparation of dried-down amplification mix preparations. en Optimize your SNP analysis. Discriminate between paired and unpaired primer ends using an enzyme optimized for allele-specific PCR. Obtain reliable results fast. Benefit from the general features of the AptaTaq DNA Polymerase System with the discriminating capabilities of a 5'-3' exonuclease activity-lacking Taq DNA Polymerase. Prepare stable amplification mixes in dry format. Use this formulation for producing dried-down amplification mixes stable at room temperature.   en N-terminal truncated Taq DNA Polymerase with reversible hot start system and no 5'-3' exonuclease activity for optimal detection of mismatches; lyo ready formulation for preparation of dried amplification mixes. en Appearance: Clear, colorless solution Storage buffer: Tris/HCl, 20 mmol/L; KCl, 100 mmol/L;EDTA, 0.1 mmol/L; DTT, 1 mmol/L; casein 1 g/L; glycerol-free; pH approximately 8.0 at +4°C Volume activity: 55±5 U/μL Aptamer concentration (HPLC): 240 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. Function 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. en