Taq Polymerase Kb Min

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PCR REAGENTS FROM NEB
Extension Rate 1 kb/min 1 kb/min 2.4 kb/min 1 kb/min 1.2 kb/min 1 kb/min 1 kb/min 1 kb/min 0.5 kb/min 1 kb/min Polymerase enables amplification of up to 40 kb PCR products with a fidelity higher than Taq DNA Polymerase alone. … Document Viewer

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Power Taq DNA Polymerase
Power Taq DNA Polymerase Code No.: GN-TAQ-100 Content : Power Taq DNA Polymerase 1 min 72℃ 1 min/kb PCR target 68℃ 1 min/kb PCR target 26~38 For Research Use Only … Content Retrieval

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AccuPrime Taq DNA Polymerase High Fidelity Cat. Nos. Size …
• For longer genomic DNA targets (>15 kb), we recommend using 2 –2.5 U of AccuPrime ™ Taq DNA Polymerase High Fidelity and increasing the extension time as specified (1 min … Access This Document

Taq Polymerase Kb Min

Taq PCR Handbook
Extension rate: 2–4 kb/min at 72°C Half-life: 10 min at 97°C; 60 min at 94°C This protocol has been optimized for amplifying long PCR products (>3 kb) using a combination of QIAGEN Taq DNA Polymerase and ProofStart DNA Polymerase … Access Full Source

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AccuStart Taq DNA Polymerase
Initial denaturation: 94ºC, 1 to 3 min PCR cycling (20 – 40 cycles:) 94ºC, 15 to 30 s 55 – 65ºC, 30s 68 – 72ºC, 1 min per kb of product length Hold 4ºC until processed for analysis Full activation of AccuStart Taq DNA polymerase occurs within 30 seconds at 94ºC; however … Access Document

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High Specificity And Robustness Of Erick B. Hu Jun E. Lee …
55-60°C, 30 s; and 68°C, for 1 min/kb. Twenty percent of each amplification reaction was analyzed by electrophoresis with a 0.5X TBE-3% agarose containing 0.5 µg/ml ethidium bromide. Unlike Taq DNA polymerase alone, AccuPrime™ Taq DNA polymerase functions effi- … View This Document

Taq Polymerase Kb Min

Power Taq DNA Polymerase
Power Taq DNA Polymerase 1.5 ml 10X Reaction Buffer with 15mM MgCl 2 1.0 ml 10mM dNTPs Mixtures (option for GN-TAQ-101) 1 min/kb PCR target 68℃ 1 min/kb PCR target 26~38 For Research Use Only … Retrieve Doc

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TaKaRa Ex Taq
Special step to denature the antibody to Taq polymerase. Example : Amplification of 1 kb DNA fragment 98℃ 10 sec. 98℃, 10 sec. 30 cycles 55℃ 30 sec. 30 cycles or68℃, 1 min. … Get Document

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Platinum Taq DNA Polymerase
kb. Cycle sequencing. It gives more uniform bands than Klenow. The high temperature extension and cycling permits Once dissociated by treatment of the Ab/enzyme mixture at 94°C for 2 min, the Taq DNA polymerase regains its … Get Doc

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JumpStart Taq DNA Polymerase (D9307) – Technical Bulletin
(minimum)* Final extension: 72 °C 1 min (minimum)* Hold 4 °C * 1 minute minimum or 1 minute per kb expected may reduce the affinity of the JumpStart Taq antibody for the Taq polymerase … Retrieve Document