FastStart Taq DNA Polymerase, 5 U/μl
from Thermus aquaticus BM, expressed in E. coli, solution
For further processing only.
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Will be supplied as ''Fast Start Taq DNA Polymerase''. Unit of measure is ''kU''.
FastStart Taq DNA Polymerase, 5 U/μl material number and pack size: Material Number Pack Size 12161508103 custom fill
The enzyme is supplied without reaction buffer. -
Hot start Taq DNA Polymerase for highly specific and sensitive amplification using PCR.
Achieve high specificity, sensitivity, and yield.
Prevent the extension of non-specifically bound primers using this hot start enzyme. - For applications see FastStart Taq DNA Polymerase, GMP Grade, 5 U/μl
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See FastStart Taq DNA Polymerase, GMP Grade, 5 U/μl
Appearance: Clear to slightly opalescent, colorless solution
Storage buffer: Tris/HCl, 20 mmol/L; KCl, 100 mmol/L; DTT, 1 mmol/L; EDTA, 0.1 mmol/L; Tween 20; 0.2% (v/v); glycerol, 50% (v/v); pH approximately 9.0 at +25°C
Volume activity: ≥5 U/μL
Unit definition: One unit Taq DNA Polymerase is defined as the amount of heat-activated enzyme that incorporates 10 nmol of total deoxyribonucleosidetriphosphates into acid precipitable DNA within 30 minutes at +75°C under standard assay conditions.
Unspecific endonucleases (λDNA): Not detectable in up to 25 U after 16 hours incubation at +37°C.
Nicking activity (pBR322 DNA): Not detectable in up to 25 U after 16 hours incubation at +37°C.
Ribonucleases (MS2 RNA): Not detectable in up to 25 U after 1 hour incubation at +37°C.
Exonucleases (3H-DNA): Not detectable in up to 15 U after 4 hours incubation at +65°C.
Function test in PCR
(50 pg human genomic DNA, 365 bp tPA fragment): Corresponds to reference
(200 ng human genomic DNA, 284 bp ApoE fragment): Corresponds to reference
Animal-derived additives: None
Stability: At -15 to -25°C within specification range for 18 months.