Maxima Sybr Green Qpcr Master Mix (2x), With Separate Rox Vial, Ready-To-Use Solution Optimized For Qpcr And 2-Step Rt-Qpcr, Each

Details:

The master mixes include maxima hot start taq dna polymerase and dntps in an optimized pcr buffer. Only template and primers need to be added. The sybr green i intercalating dye allows for dna detection and analysis without using sequence-specific probes.Maxima hot start taq dna polymerase in combination with an optimized buffer ensures pcr specificity and sensitivity. Dutp is included in the mix for optional carry-over contamination control using uracil dna glycosylase (udg). The use of maxima sybr green qpcr master mixes in real-time pcr ensures reproducible, sensitive and specific quantification of genomic, plasmid, viral, and cdna templates. Maxima sybr green qpcr master mixes are compatible with most real-time thermal cyclers.Specificity - maxima hot start taq dna polymerase and the optimized buffer eliminate non-specific amplification and formation of primer dimerssensitivity - detects low copy number targetswide linear range - accurate quantification across 9 orders of magnitudereproducibility and convenience - ready-to-use 2x master mix