Construction of DNA-Origami: Difference between revisions
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*'''''2. Purifying''''' | *'''''2. Purifying''''' | ||
#''' Six times ultrafiltration using a 100 kDa molecular-weight-cutoff filter(MWCO)''' | #''' Six times ultrafiltration using a 100 kDa molecular-weight-cutoff filter(MWCO)''' | ||
#''' 2% agarose gel electrophoresis running at 90 V for 2 h''' | #''' 2% agarose gel electrophoresis running at 90 V for 2 h.''' Louding(Marker, Scaffold, Samples without ultrafiltration, Samples with ultrafiltration, Marker) | ||
#''' Image development''' | #''' Image development''' | ||
* | * | ||
Revision as of 13:58, 25 November 2025
Construction Material
Scaffold
- P8064 Powder and Stock Solution at 150 nM
Staples
- Stock solutions(Hexagonal-prism DNA origami) in three 96‑well plates at 100 uM
- Schematic Diagram

For detailed information, please refer to the shared "Origami" file on Feishu
- Stock solutions (Unmodified hexagonal‑prism DNA origami) in EP tube at 500 nM
Fabrication
- 1. Folfing
| Material | Volume(100 μL) | Volume(50 μL) |
|---|---|---|
| Staples (500 nM) | 25 μL | 12.5 μL |
| P8064 (150 nM) | 10 μL | 5 μL |
| 10X PBS | 10 μL | 5 μL |
| H2O | 55 μL | 27.5 μL |
- Program folding in PCR thermocycler : The mixed sample was put on a thermal ramp starting with a rapid heat denaturation at 80 °C for 5 min followed by cooling from 80 °C to 60 °C over 20 min, then slow cooling from 60 °C to 24 °C over 14 h.
- 2. Purifying
- Six times ultrafiltration using a 100 kDa molecular-weight-cutoff filter(MWCO)
- 2% agarose gel electrophoresis running at 90 V for 2 h. Louding(Marker, Scaffold, Samples without ultrafiltration, Samples with ultrafiltration, Marker)
- Image development
- 3. TME
- Observation by negative‑stain transmission electron microscopy