SapphireAmp Fast PCR Master Mix is designed for fast, streamlined PCR, and is, therefore, ideal for applications such as colony PCR. It contains a hot-start PCR enzyme, optimized buffer, dNTPs, along with a blue gel-loading dye and density reagent, in a convenient 2X premix format.
Reactions are assembled by simply mixing primers and DNA template with SapphireAmp Fast PCR Master Mix. For rapid and convenient screening, the amplification reactions can be loaded directly onto an agarose gel immediately after amplification without purification, or digested directly with restriction enzymes.
For E. coli-based colony PCR, inserts up to ~5 kb in length are easily screened; colony PCR can be performed in about an hour.
For human genomic DNA, amplification of 2-kb targets can be completed in one hour; amplifications of up to 6 kb are possible.
Overview
Hot-start PCR master mix is optimized for fast PCR
Colony PCR can be completed in half the time required for conventional Taq DNA polymerase
Convenient protocol eliminates purification steps with no reduction in yield
Restriction enzyme digestion of the PCR products can be performed directly in the PCR buffer
Reactions can be directly loaded onto a gel without purification or the addition of other reagents
SapphireAmp Fast PCR Master Mix is designed for fast, streamlined PCR, and is, therefore, ideal for applications such as colony PCR. It contains a hot-start PCR enzyme, optimized buffer, dNTPs, along with a blue gel-loading dye and density reagent, in a convenient 2X premix format.
Reactions are assembled by simply mixing primers and DNA template with SapphireAmp Fast PCR Master Mix. For rapid and convenient screening, the amplification reactions can be loaded directly onto an agarose gel immediately after amplification without purification, or digested directly with restriction enzymes.
For E. coli-based colony PCR, inserts up to ~5 kb in length are easily screened; colony PCR can be performed in about an hour.
For human genomic DNA, amplification of 2-kb targets can be completed in one hour; amplifications of up to 6 kb are possible.
Overview
Hot-start PCR master mix is optimized for fast PCR
Colony PCR can be completed in half the time required for conventional Taq DNA polymerase
Convenient protocol eliminates purification steps with no reduction in yield
Restriction enzyme digestion of the PCR products can be performed directly in the PCR buffer
Reactions can be directly loaded onto a gel without purification or the addition of other reagents