928100
Gold nanoparticles
30 nm diameter, Alkyne functionalized, 1 ML, OD 50, in water
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About This Item
UNSPSC Code:
12141717
NACRES:
NA.22
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Quality Level
description
Alkyne surface density: 1/nm2
concentration
in water
OD
50
core diam.
30 nm , coefficient of variance <12%
diameter
30 nm
λmax
526 nm
PDI
<0.200
functional group
alkyne
storage temp.
2-8°C
InChI
1S/Au
InChI key
PCHJSUWPFVWCPO-UHFFFAOYSA-N
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General description
Alkyne functionalized gold nanoparticles are suitable for covalent conjugation of any azide-tagged molecule through Cu(I)-catalyzed click chemistry. These gold nanoparticles allow for rapid generation of gold conjugates for subsequent use in downstream assays.
Alkyne functionalized gold nanoparticles are more than 95% spherical and have uniform size distribution (CV <12%).
Alkyne functionalized gold nanoparticles are more than 95% spherical and have uniform size distribution (CV <12%).
Application
Ideal for development of gold conjugates for use in applications such as blotting, lateral flow assays, microscopy, and transmission electron microscopy (TEM).
Storage and Stability
When stored for a long period of time gold nanoparticles may sediment at the bottom of the vial, which is especially prominent for larger particle sizes. Prior to use, re-suspend the sedimented particles by thorough mixing until a homogenous solution is obtained.
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 2
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Gold nanoparticles: synthesis and applications in drug delivery.
Khan A K, et al.
Tropical Journal of Pharmaceutical Research, 1169-1177 (2014)
Wilson Luo et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(5), 1052-1059 (2016-10-12)
In this study, we report the design, synthesis, and characterization of small 3 nm water soluble gold nanoparticles (AuNPs) that feature cyclopropenone-masked strained alkyne moieties capable of undergoing interfacial strain-promoted cycloaddition (i-SPAAC) with azides after exposure to UV-A light. A strained
Mingmin Li et al.
Nanotheranostics, 3(1), 113-119 (2019-03-23)
Surface-enhanced Raman spectroscopy (SERS) has proven a powerful tool for multiplex detection and imaging due to its narrow peak width and high sensitivity. However, conventional SERS reporters are limited to thiolated compounds, which have limitations such as chemical stability and
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