Undecagold labeling reagents are now available in three different packages: 50 nmol for larger labeling experiments, 5 X 10 nmol for several smaller labeling experiments, or in single 10 nmol vials so you can try these reagents on a smaller scale for a low price.
Undecagold (Au11) is smaller than Nanogold®, with a core of 11 gold atoms only 0.8 nm in diameter. It is ideal for ultra-high-resolution EM work such as scanning transmission electron microscopy, or for resolving elements of large structures by TEM in conjunction with image processing. Undecagold has been used to see the biotin binding sites on avidin to 1 nm resolution by electron microscopy. It is prepared in a form with one reactive arm for cross-linking to a specific site on a target molecule, and is available with different reactivities for labeling different sites.
Note: Single undecagold clusters are not routinely visualized directly in the TEM. Undecagold may be seen upon image processing of protein helices and crystals, or visualized en masse if there is a bulk deposition such as staining of an organelle. Also, undecagold develops more slowly and with less final silver deposition than Nanogold®. Therefore, for many applications we recommend Nanogold®.
Structure of undecagold showing the [Au11] core, coordinated ligands and peripheral reactive group (maleimide).
Site specific covalent labeling with choice of reactivities.
Applications
Scanning transmission electron microscopy (STEM). [References]
Labeling of F-actin at the Cys-374 residue by reacting with monomalemido undecagold; data was collected from frozen hydrated samples in the EM and image processing used to map the distribution of label (see: Milligan, R.A., et al.: Nature, 348, 217-221 (1990)). [Other references]
Labeling of a cysteine in cytochrome oxidase crystals and EM visualization in uranyl acetate/glucose using image processing. [References]
tRNA labeling with undecagold using a modified nucleic acid base (see: Blechschmidt, B., et al.: J. Struct. Biol., 110, 84-89 (1993)). [Other references]
Localization of the C terminus of the assembly domain of hepatitis B virus capsid protein by electron microscopy, with image processing (see: Zlotnick, A., et al.: Proc. Natl. Acad. Sci. USA, 94, 9556-9561 (1997)).
Isomorphous heavy atom replacement in crystallography of large structures by EM crystallography, single particle alignment work, or X-ray diffraction. Provides a signal much greater than a single heavy atom label (see: Thygesen, J., et al. [review]: Structure, 4, 513-518 (1996)). [Other references]
Labeling carbohydrates on a glycoprotein: sugars are first oxidized to produce aldehydes, which react with the monamino undecagold. [References]
The simple-to-use activated Maleimido-undecagold reagent is used for labeling thiols with undecagold. It will specifically label free sulfhydryls in proteins, antibodies, peptides, substrates or other molecules containing a free thiol. For use, it is simply dissolved in water and mixed with the material to be labeled for a few hours. Undecagold conjugates are then isolated by gel filtration.
Applications:
Create your own small gold probes by linking Au11 to your primary antibody Fab' fragments.
Label proteins directly for high resolution, site specific identification.
Label peptides containing cysteine.
Monomaleimido Undecagold
Single vial (50 nmol)
Monomaleimido Undecagold
Multiple experiments (5 x 10 nmol)
Positively and negatively charged undecagold may be used as ionic labels, to stain biological structures with opposite charges. Positive undecagold has multiple amines on its surface and may therefore stain negatively charged features; negatively charged undecagold has multiple carboxyl groups, and will stain features containing many positively ionizing groups.
Non-fuctionalized undecagold is an inert, stable form of the undecagold particle with no reactive chemical functionalities or specific affinity properties.
Applications:
As a size standard for calibration in high-resolution electron microscopy.
Sizing pores (see: Schwartz, M. P., and Matouschek, A.: The dimensions of the protein import channels in the outer and inner mitochondrial membranes. Proc. Natl. Acad. Sci. USA, 96, 13086-13090 (1999)). [Complete references]
For tracing contiguous interior spaces in cells and tissues.
Nanoprobes does not stock undecagold conjugates, but we will be glad to prepare them to order as a custom synthesis. Let us know your needs, and we'll give you a quote: Use our online form, e-mail us at tech@nanoprobes.com, or call us at 877-447-6266 (US toll-free number) or (631) 205-9490. We look forward to working with you!
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