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文献和实验Antibody to an equal amount of Taq DNA polymerase units. ForTaq DNA polymerase at 5 unit per μl, prepare a 1:1 mixture. Mix well using a Vortex Mixer. 3. Add the following components to a sterile 0.5-ml microcentrifuge tube:
This is a protocol from Engelke et.al.(1990)which was modified by Dr.Baron.The enzyme has been used for RT-PCR,genotyping and cloning.Solutions1000X IPTG0.5M IPTG 1.19g IPTGup to 10 ml wih sterile Qfilter and store at -20℃Buffer A50 mM Tris 7.9 25
Home-made Taq Polymerase Purification
( 8K / 15mins / 4°C). 7) Add 1.86mg of KCl / ml of supernatant. 8) Aliquot equal volumes of supernatant into each of 2 x 250ml centrifuge tubes (preferably conical) containing 75ml of washed Sigma DP-1 cation exchange resin (packed
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