Diversify PCR Random Mutagenesis Kit for sequence mutations
The Diversify PCR Random Mutagenesis Kit employs a nontoxic method for mutagenizing sequences of up to 4.0 kb in length. The kit broadly distributes all possible mutations without creating hot spots. By allowing you to manipulate mutagenic conditions, the Diversify PCR Random Mutagenesis Kit provides optimal mutagenesis of sequences over an exceptionally broad size range. Select mutation rates from two to eight mutations per 1,000 bp simply by varying the amounts of two key reagents-manganese (Mn2+) and dGTP.
The Diversify PCR Random Mutagenesis Kit employs a nontoxic method for mutagenizing sequences of up to 4.0 kb in length. The kit broadly distributes all possible mutations without creating hot spots. By allowing you to manipulate mutagenic conditions, the Diversify PCR Random Mutagenesis Kit provides optimal mutagenesis of sequences over an exceptionally broad size range. Select mutation rates from two to eight mutations per 1,000 bp simply by varying the amounts of two key reagents—manganese (Mn2+) and dGTP (Cadwell and Joyce 1992; Leung, Chen, and Goeddel 1989).
The Diversify PCR Random Mutagenesis Kit contains our Titanium Taq PCR system to reliably amplify DNA fragments of up to 4.0 kb in length. This extended amplification range makes the Diversify kit ideal for mutating operons, plasmids, and sequences corresponding to large proteins, in addition to short DNA fragments. The kit also contains a rapid control reaction that allows the relative comparison of mutation rates in the control fragment in just two hours following PCR. In addition to the Titanium Taq polymerase mix, the Diversify PCR Random Mutagenesis Kit includes all of the reagents and buffers needed for mutagenesis.
Overview
- Controlled, random mutagenesis for investigating protein function
- Precise control of mutation rate
- No mutational hot spots
- Obtain all possible base substitutions
More Information
Applications
- Random mutagenesis
References
Cadwell, R. C. & Joyce, G. F. Randomization of genes by PCR mutagenesis. PCR Methods Appl. 2, 28–33 (1992).
Leung, D., Chen, E., and Goeddel, D. V. PCR-based random mutagenesis using skewed nucleotide concentrations. Technique 1, 1–15 (1989).
Product citations
Mo, J. Y., Maki, H. & Sekiguchi, M. Mutational specificity of the dnaE173 mutator associated with a defect in the catalytic subunit of DNA polymerase III of Escherichia coli. J. Mol. Biol. 222, 925–36 (1991).
Additional product information
Please see the product's Certificate of Analysis for information about storage conditions, product components, and technical specifications. Please see the Kit Components List to determine kit components. Certificates of Analysis and Kit Components Lists are located under the Documents tab.
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