Mutant Library Construction Service

Mutant Library Construction Service
group name
Pharmaceutical Chemicals
Min Order
1 gram
brand name
CD Genomics
payment method
update time
Mon, 26 Jan 2015 00:53:43 GMT

Packging & Delivery

  • Min Order1 gram


In vitro molecular optimization is a very efficient means of generating mutant proteins.


In vitro molecular optimization is a very efficient means of generating mutant proteins with improved or novel properties, identifying regulatory sequences, and probing for structurally and functionally critical residues. Mutant libraries constructed using the in vitro molecular optimization method provide one useful approach to the systematic study of protein properties, regulation, and function.

Our Mutant Library Service Includes:

1. Site-directed Mutagenesis Libraries
CD Genomics combines its    expertise in de novo gene synthesis and site-directed    mutagenesis into an excellent site-directed mutagenesis library construction    service. The site-directed mutagenesis  library offers a great platform for    protein function and active center studies. In these libraries, any given    residue can be substituted with any of other 19 common amino acids, creating    systematic combinations of amino acid mutations that reveal any significant    pattern.

2. Scanning Point Mutation Libraries 
Scanning point mutation is a systematic means of improving protein performance. It outperforms standard alanine/cysteine scanning by replacing each amino acid with all 20 amino acids simultaneously. This technique provides a detailed profile of each amino acid at the position. For each codon of interest, a small, site-saturated library is constructed. This library can be delivered as a pool or in a separated format for any substitution variant (19 in total). The application of CD Genomics's expertise in de novo gene synthesis to the field of sequential permutation scanning allows us to provide superb sequential permutation scanning library construction services.

3. Randomized and Degenerated Libraries
With our advanced degenerated oligonucleotide techniques, CD Genomics can generate any form of randomization or degeneration of full-length  gene in a synthetic DNA fragment. This permits controlled, highly precise randomization within oligonucleotides. CD Genomics's in vitro library synthesis technology can introduce random substitutions on a controlled level with maximum flexibility. The mutation frequency can be set to any value between 1 and 20 mutations per kb. A peer group of 48, 96, or 192 individual transformants is sequence-verified.