GeneArt® Controlled Randomization Service
![]() | Random SubstitutionsGeneArt® Controlled Randomization technology allows you to accurately direct the effective frequency of random nucleotide substitutions. And unlike error-prone PCR, you decide exactly which part(s) of the gene are affected—randomize the entire open reading frame or confine the mutagenesis to specific regions. |

Get Your Project Started
| Please download the questionnaire to submit project information. For secure data transfer please register at our customer portal. |
For further information regarding this service or the order process, please contact christian.kranz@lifetech.com.
Libraries Are Available Cloned or Ready to Clone
| GeneArt® Controlled Randomization Ready-to-Clone Library |
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| GeneArt® Controlled Randomization Cloned Library |
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Applications
- Diversify antigen-binding sites of antibodies
- Improve physicochemical protein properties such as solubility, heat stability, and activity in industrial environments
- Enhance function, such as promoter activity and enzymatic properties
- Optimize antibody affinity (in vitro affinity maturation)
- Humanize antibodies
- Prolong half-life of therapeutics for in vivo environments
- Improve enzymes for industrial use
- Modify enantioselectivity of enzymes
- Induce changes to alter proteins from patented sequences
Advantages
- Library diversity of up to 1011 variants
- Precise selection of the average mutation rate (number of changes per construct)
- Random mutagenesis throughout construct, or limited to defined positions
- Transition/transversion ratio of 1:2
- Fewer silent mutations
- Low ancillary mutation rate
- Fast production times
Quality Control
All GeneArt® Controlled Randomization products are sequenced and subjected to statistical analysis to help ensure that they meet the following quality benchmarks:
- Sequencing of up to 96 individual transformants to verify that customer’s specifications regarding nucleotide content and amino acid encoding have been met, and that sequence integrity of unmutated portions of the construct meets minimum requirements
- Bulk sequencing to verify that nondegenerated portions of the construct have the correct sequence and randomized portions meet customer’s specifications and maintain an open reading frame
- Real-time PCR prior to amplification to verify that library diversity objectives have been me
