Assembly and crystallization of NP superlattices
This protocol is extracted from research article:
Unusual packing of soft-shelled nanocubes
Sci Adv, May 17, 2019; DOI: 10.1126/sciadv.aaw2399

The assembly was obtained by mixing equal molar amounts of type A and type B DNA-functionalized Au NCs, and a linker Ln in a certain mole ratio of linker/type A (or B) DNA-functionalized NCs. The NCs were allowed to aggregate at room temperature. The samples were then annealed at a temperature ~3° to 5°C below the melting temperature of the assembled particles for a period of 30 min to several hours, depending on the sample. The annealed samples were transferred with buffer to a quartz capillary (1.0-mm diameter) and sealed with wax for SAXS measurements.

Note: The content above has been extracted from a research article, so it may not display correctly.



Q&A
Please log in to submit your questions online.
Your question will be posted on the Bio-101 website. We will send your questions to the authors of this protocol and Bio-protocol community members who are experienced with this method. you will be informed using the email address associated with your Bio-protocol account.



We use cookies on this site to enhance your user experience. By using our website, you are agreeing to allow the storage of cookies on your computer.