http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2022205578-A1

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filingDate 2021-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e266d16b848ba11ddff17d76483ca795
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publicationDate 2022-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2022205578-A1
titleOfInvention High-throughput automated gene synthesis apparatus based on cluster array
abstract A high-throughput automated gene synthesis apparatus based on a cluster array. The high-throughput gene synthesis apparatus comprises a substrate and a microwell plate, wherein the substrate is provided with several clusters of microwells (1); a sidewall surface of the microwell (1) is chemically modified and is then used as a solid-phase carrier for nucleic acid synthesis, or the microwell (1) is filled with solid-phase carriers; and the several clusters of microwells (1) are arranged in a cluster array, each cluster of microwells (1) has the same size as that of each hole (2) on the microwell plate, and the position of each cluster of microwells (1) corresponds to the position of each hole (2). When oligonucleotides are synthesized using the apparatus, the synthesized oligonucleotides are automatically recovered into a standard SBS plate (a 96-well plate, a 384-well plate, a 1536-well plate, etc.) having a corresponding size under the apparatus, thereby forming oligonucleotide pools required for each gene. The yield of the oligonucleotides is at a pmoL level, and is sufficient for direct subsequent gene assembly by means of polymerase cycling assembly (PCA) or ligase chain reaction (LCR) without amplification. The oligonucleotides which have been subjected to error correction can thus be used for full-length gene splicing, thereby realizing high-throughput automated gene synthesis.
priorityDate 2021-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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