Taq master mix is made from Krishgen Biosystems Taq DNA polymerase which is purified from the cloned Thermos aquaticus DNA polymerase gene expressed in E. coli. This mix contains all reaction components required for PCR, which includes reaction buffer, dNTP, gel loading dye, stabilizer and sediment in addition to Taq DNA polymerase. The loading dye migrates through 1.0% agarose gel run in a 0.5XTBE buffer at approximately the same rate as the DNA which is 300bp in length. It is recommended for use in routine PCR for amplifying a 10kb product, TA cloning and primer extensions.
0.5 ml x 2 tubes
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