Compositions and methods for nucleic acid amplification
US-2016333340-A1 · Nov 17, 2016 · US
US9670517B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-9670517-B1 |
| Application number | US-201514865127-A |
| Country | US |
| Kind code | B1 |
| Filing date | Sep 25, 2015 |
| Priority date | Jan 16, 2012 |
| Publication date | Jun 6, 2017 |
| Grant date | Jun 6, 2017 |
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The invention provides methods for the synthesis of long oligonucleotides, genes and gene fragments. The methods include the manufacture of genes or gene fragments that can be then inserted into a variety of vectors.
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What is claimed is: 1. A method of synthesizing a gene block of a desired sequence greater than 100 bases, the method comprising: a) providing a plurality of solid supports, wherein at least one solid support contains between 1-8% by weight controlled pore glass; b) synthesizing oligonucleotides on the solid supports, wherein the oligonucleotides comprise a set of oligonucleotides that are partially complementary to at least one other oligonucleotide in the set, and the set of oligonucleotides as a group contain the desired sequence of the gene block; c) detaching the oligonucleotides from the solid supports; d) combining the oligonucleotides under conditions to synthesize the gene block. 2. The method of claim 1 wherein at least one solid support contains 5-8% by weight controlled pore glass. 3. The method of claim 1 wherein the gene block is combined with additional gene blocks to form a longer gene block. 4. The method of claim 1 further comprising performing an error correction step after combining the oligonucleotides. 5. The method of claim 1 wherein the gene block is greater than 200 bases. 6. The method of claim 1 wherein the gene block is greater than 400 bases. 7. The method of claim 1 wherein the gene block is greater than 500 bases.
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Nucleic acid amplification reactions · CPC title
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