2X PCR Master Mix with Loading Dye

  • 2X SuperRed PCR MasterMix with Loading Dye(Red)

    2X SuperRed PCR MasterMix with Loading Dye(Red)

    SuperRed PCR Master Mix (2x) is a 2× concentrated, optimized mixture composed of Taq DNA Polymerase, the NH4+ buffer system, dNTPs and MgCl2. An inert red dye and a stabilizer are also present to allow direct loading of the final products onto an agarose gel for analysis. The advantages of SuperRed PCR Master Mix (2x) include high convenience, sensitivity, specificity and stability. It minimizes man-made errors during PCR operating process. SuperRed PCR Master Mix (2x) is suitable for routine PCR reaction, amplification of complex templates such as GC rich templates (>60%) and templates with secondary structure, and large-scale gene detection.

  • 2X Tools Taq PCR MasterMix with Loading Dye(Blue)

    2X Tools Taq PCR MasterMix with Loading Dye(Blue)

    2× ToolsTaq PCR MasterMix is a 2× concentrated, optimized mixture composed of ToolsTaq DNA polymerase, dNTPs, MgCl2, reaction buffer, PCR reaction enhancer, optimizer and stabilizer. The advantages of 2× ToolsTaq PCR MasterMix include high convenience, sensitivity, specificity and stability. It minimizes man-made errors during PCR operating process. 2× ToolsTaq PCR MasterMix is suitable for routine PCR reaction, amplification of complex templates such as GC-rich templates (>60%) and templates with secondary structure, and large-scale gene detection.

  • 2X Extra Long Taq PCR MasterMix with Loading Dye(Blue)

    2X Extra Long Taq PCR MasterMix with Loading Dye(Blue)

    2× EtraLong Taq PCR MasterMix is a 2× concentrated, optimized mixture composed of ExtraLong Taq DNA polymerase, dNTPs, MgCl2, reaction buffer, PCR reaction enhancer, optimizer and stabilizer. The advantages of2× EtraLong Taq PCR MasterMix include high convenience, sensitivity, specificity and stability. It minimizes man-made errors during PCR operating process. 2× EtraLong Taq PCR MasterMix is suitable for long-range PCR reaction, amplification of complex templates such as GC-rich templates (>60%) and templates with secondary structure and large-scale gene detection.

  • 2X GC MasterMix with Loading Dye(Blue)

    2X GC MasterMix with Loading Dye(Blue)

    2× GC PCR MasterMix is a 2× concentrated, optimized mixture composed of GeneTaq Plus DNA polymerase, dNTPs, MgCl2, reaction buffer, PCR reaction enhancer, optimizer and stabilizer. The advantages of 2× GC MasterMix include high convenience, sensitivity, specificity and stability. It minimizes man-made errors during PCR operating process. 2× GC PCR MasterMix is suitable for routine PCR reaction, amplification of complex templates such as GC-rich templates (>60%) and templates with secondary structure.

  • 2X Super Hi-Fi Taq PCR MasterMix with Loading Dye(Blue)

    2X Super Hi-Fi Taq PCR MasterMix with Loading Dye(Blue)

    2× Super Hi-Fi Tag PCR MasterMix is a 2× concentrated, optimized mixture composed of Super Hi-Fi Tag DNA polymerase, dNTPs, MgCl2, reaction buffer, PCR reaction enhancer, optimizer and stabilizer. The advantages of 2×Super Hi-Fi Tag PCR MasterMix include high convenience, sensitivity, specificity and stability. It minimizes man-made errors during PCR operating process. 2×Super Hi-Fi Tag PCR MasterMix is suitable for routine PCR reaction, amplification of complex templates such as GC-rich templates (>60%) and templates with secondary structure.

  • 2x HotStart Taq PCR MasterMix with loading dye (Blue)

    2x HotStart Taq PCR MasterMix with loading dye (Blue)

    The advantages of 2×HotStart PCR MasterMix include high convenience, sensitivity, specificity and stability. It minimizes man-made errors during PCR operating process. HotStart inhibitor blocks the substrate binding site of HotStart Taq DNA polymerases in a temperature-dependent manner. Inactive polymerase-inhibitor complexes are formed at temperatures < 40°C, where the affinity of HotStart inhibitor for HotStart Taq DNA polymerase is higher than the binding affinity of the template DNA. Between 40°C and 55°C the HotStart inhibitor competes with the template DNA for binding to the Taq DNA polymerase, thereby shifting the binding equilibrium towards complex formation with only target-specific primed template DNA. This minimizes the non-specific amplification in PCR and ensures high sensitivity and specificity.