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DNA Mutagenesis

Random Mutagenesis Kits (隨機突變分析套組)

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.
經過30億年的演變,自然界已經存在且正產生過多的蛋白質,它透過一些簡單程序,即反復循環之隨機誘發突變,然後在生物體內選擇較優越的功能蛋白質核酸譯碼。這個自然演變的例子,在過去20年裡引導科學家發展體外蛋白質變異交換策略應用。經過多樣性的策略應用,主要有三大技術被應用。

dNTP-Mutagenesis、Error-Prone、DNA-Shuffling

Cat. No. PP-101  JBS dNTP-Mutagenesis Kit  15 reactions 

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%.

Cat.No. PP-102  JBS Error-Prone Kit  15 reactions

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%.

Cat.No. PP-103   JBS DNA-Shuffling Kit   15 reactions

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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