摘要:
The invention relates to a method for marking a substrate with a unique library of nucleic acid sequence tags comprising: providing a library of nucleic acid sequence tags, comprising at least two different groups of nucleic acid sequence tags that each comprise a plurality of nucleic acid sequence tags, wherein each of said nucleic acid sequence tags comprises a defined nucleic acid motif in at least a first and a second characteristic position, and wherein outside of said at least two characteristic positions each nucleic acid sequence tag comprises a random nucleic acid sequence, wherein the combination of the nucleic acid motifs of the at least first characteristic position and the at least second characteristic position of a nucleic acid sequence tag is characteristic and unique for the group of said nucleic acid sequence tag, and marking the substrate with the unique nucleic acid library by applying the nucleic acid sequence tag library to the substrate. The invention further relates to a packaging article comprising a substrate marked according to the method of the present invention and different kits for applying and validating a substrate tagged according to the present invention.
摘要:
Described is a method for generating a multiple-gene assembly in a single DNA construct, a kit and a single DNA construct generated by the method. Different assembly methods are known in the state of the art but user has to decide between scar free, sequence independent methods, which require the time consuming individual design of every assembly and modular approaches, which generate scar sequences and require laborious parts domestication. In order to overcome these drawbacks a method for generating a multiple-gene assembly in a single DNA construct is provided that contains freely designed scar-free level 0 assembly units in a predefined order, determined by flanking homology regions and which is sequence-independent.