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DNA Mutagenesis - Random Mutagenesis Kits |
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Random Mutagenesis Kits
Within three billion years of evolution, nature has produced a plethora of proteins simply by repeated cycles of random mutagenesis followed by in vivo selection for superior function of the encoded proteins. This example of natural evolution has guided researchers within the last two decades to develop strategies for in vitro permutation of proteins.
Among the variety of strategies applied, three major powerful techniques have emerged.
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JBS dNTP-Mutagenesis Kit Random Mutagenesis by dNTP Analogs | |  |
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Kit |
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PP-101 |
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15 reactions |
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240,00 |
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 |  | Store at -20°C, avoid frequent thawing and freezing
Polymerase
10x Mutagenesis buffer
dNTP mix
dPTP
8-oxo-dGTP
PCR grade water |  | JBS dNTP-Mutagenesis Kit is based on the incorporation of the mutagenic dNTP analogs 8-oxo-dGTP and dPTP into an amplified DNA fragment by PCR. The mutagenic dNTPs are eliminated by a second PCR step in the presence of the four natural dNTPs only, resulting in a rate of mutagenesis of up to 20%. |  |  |  |
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JBS Error-Prone Kit Random Mutagenesis by Error-Prone PCR | |  |
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Kit |
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PP-102 |
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15 reactions |
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190,00 |
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 |  | Store at -20°C, avoid frequent thawing and freezing
Polymerase
10x Reaction buffer
10x Error-prone solution
dNTP error-prone mix
PCR grade water |  | JBS Error-Prone Kit introduces mutations in the gene of interest using modified PCR reaction conditions. An increased MgCl2 concentration, the addition of MnCl2 and the unbalanced ratio of dNTPs induce an increased error-rate of the DNA-polymerase. The rate of mutagenesis achieved by error-prone PCR is in the range of 0.6-2.0%. |  |  |  |
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JBS DNA-Shuffling Kit Random Mutagenesis by DNA Shuffling | |  |
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Buy |
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Kit |
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PP-103 |
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15 reactions |
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240,00 |
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 |  | Store at -20°C, avoid frequent thawing and freezing
DNase I
10x Digestion buffer
DNase stop solution
Polymerase
10x Shuffling buffer
dNTP mix
PCR grade water |  | JBS DNA-Shuffling Kit is designed to generate gene libraries by random fragmentation of one gene or a pool of related genes. A controlled fragmentation of the DNA is followed by a random reassembly in a self-priming PCR reaction. This method allows the recombination of sequences from different, related genes. The overall rate of mutagenesis is approx. 0.7%. |  |  |
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