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A set of experimentally validated, mutually orthogonal primers for combinatorially specifying genetic components
Author(s) -
Subu Subramanian,
William P. Russ,
Rama Ranganathan
Publication year - 2018
Publication title -
synthetic biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.769
H-Index - 8
ISSN - 2397-7000
DOI - 10.1093/synbio/ysx008
Subject(s) - synthetic biology , oligonucleotide , computational biology , multiplex , computer science , scalability , gene , biology , throughput , modular design , genetics , telecommunications , database , wireless , operating system
The design and synthesis of novel genes and deoxyribonucleic acid (DNA) sequences is a central technique in synthetic biology. Current methods of high throughput gene synthesis use pooled oligonucleotides obtained from custom-designed DNA microarray chips, and rely on orthogonal (non-interacting) polymerase chain reaction primers to specifically de-multiplex, by amplification, the precise subset of oligonucleotides necessary to assemble a full length gene. The availability of a large validated set of mutually orthogonal primers is therefore a crucial reagent for high-throughput gene synthesis. Here, we present a set of 166 20-nucleotide primers that are experimentally verified to be non-interacting, capable of specifying 13 695 unique genes. These primers represent a valuable resource to the synthetic biology community for specifying genetic components that can be assembled through a scalable and modular architecture.

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