Efficient and rapid method for assembling and cloning double-stranded DNA fragments
US9951327B1 · kind B1 · utility
1Cited by
92References
18Claims
0Family size
Assignee
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Key dates
| Filing date | Jul 17, 2015 |
| Grant date | Apr 24, 2018 |
| Priority date | — |
| Expiry date | May 16, 2036 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12Y605/01001
- WIPO fieldBiotechnology
- WIPO sectorChemistry
Abstract
The invention is directed to an in vitro method for joining a first set of double-stranded (ds) DNA molecules. Small molecules acting as chaperone agents are identified that promote efficient and rapid assembly (that is, joining) of overlapping double-stranded DNA fragments.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.