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Alexa Fluor 647 FluoroNanogold™. 2-in-1 Labeling for Super-Res + TEM

Alexa Fluor® 488-FluoroNanogold™ IgG goat anti-rat

Fluorescent labels PLUS Nanogold® – covalently bound. Make your target visible in almost any microscope!

Nanoparticle Size: 1.4 nm
Reactive Groups: Alexa Fluor® 488
Unit Sizes: 0.5 mL

Alexa Fluor® 488-FluoroNanogold™ IgG goat anti-rat

Alexa Fluor 647 FluoroNanogold™. 2-in-1 Labeling for Super-Res + TEM

Fluorescent labels PLUS Nanogold® – covalently bound. Make your target visible in almost any microscope!

Nanoparticle Size: 1.4 nm
Unit Sizes: 0.5 mL

Alexa Fluor® 488-FluoroNanogold™ IgG goat anti-rat

7207-0.5ML

0.5 mL

$ 378.00

Add to cart

Alexa Fluor® 488-FluoroNanogold™ IgG goat anti-rat

7207-1ML

1.0 mL

$ 630.00

Add to cart
  • 7207-0.5ML

Alexa Fluor® 488-FluoroNanogold™ IgG goat anti-rat

0.5 mL

$ 378.00

Add to cart
  • 7207-1ML

Alexa Fluor® 488-FluoroNanogold™ IgG goat anti-rat

1.0 mL

$ 630.00

Add to cart

Grow the size - Keep the precision

Combine nanoparticle developers with Nanogold® labels

Easy, archival developers for any scope or blots
  • GoldEnhance™:
    Simple. Superior. Precision nanoparticle enhancement
    Sharp, archival staining of blots or easy viewing in any scope.
  • Silver Enhancement:
    Precision nanoparticles, not colloidal silver blobs: precise development for any scope.
Product Information
  • Hirano K, Kinoshita T, Uemura T, Motohashi H, Watanabe Y, Ebihara T, Nishiyama H, Sato M, Suga M, Maruyama Y, Tsuji NM, Yamamoto M, Nishihara S, Sato C. Electron microscopy of primary cell cultures in solution and correlative optical microscopy using ASEM. Ultramicroscopy. 2014 Aug;143:52-66. doi: 10.1016/j.ultramic.2013.10.010. Epub 2013 Oct 22. PMID: 24216127.
    https://pubmed.ncbi.nlm.nih.gov/24216127/

Alexa Fluor® 488-FluoroNanogold™ IgG goat anti-rat

FluoroNanogold™ Combination Labels

Covalently bound, Nanogold® + fluorescent secondary antibodies

Precision meets flexibility

Alexa Fluor® 488 FluoroNanogold™

2-in-1 immunolabeling!

Our new Alexa Fluor® FluoroNanogold™ conjugates will give you greatly enhanced performance compared with conventional fluorophores.

Benefit from greatly improved fluorescence properties, combined with a new level of freedom from background and non-specific binding.

  • Increased fluorescence signal and higher quantum yield – ideal for scarce targets or dynamic systems where exposure needs to be restricted.
  • Fluorescence remains high and consistent across wider pH range.
  • Improved solubility means reduced non-specific interactions, lower background and higher signal-to-noise ratios.
  • Uses fluorescein filter sets.
  • Available in 1 mL or affordable 0.5 mL sizes.
Left: Structure of Alexa Fluor® 488 and Nanogold® - Fab', showing covalent attachment of components. Right: Fluorescent staining obtained using combined combined Alexa Fluor® 488 and Nanogold® - Fab' tertiary probe. The specimen is a slide from the NOVA Lite ANA HEp-2 test, an indirect immunofluorescent test system for the screening and semi-quantitative determination of anti-nuclear antibodies (ANA) in human serum (see ). The slide was stained using positive pattern control human sera, a Mouse anti-Human secondary antiboidy, and combined Alexa Fluor® 488 and Nanogold® - Fab' tertiary probe. Specimens were washed with PBS (30 minutes) between each step, then blocked by the addition of 7 % nonfat dried milk to the tertiary antibody solution (original magnification 400 X).

Left: Structure of Alexa Fluor® 488 and Nanogold® – Fab’, showing covalent attachment of components.

Right: Fluorescent staining obtained using combined combined Alexa Fluor® 488 and Nanogold® – Fab’ tertiary probe. The specimen is a slide from the NOVA Lite ANA HEp-2 test, an indirect immunofluorescent test system for the screening and semi-quantitative determination of anti-nuclear antibodies (ANA) in human serum (see ). The slide was stained using positive pattern control human sera, a Mouse anti-Human secondary antiboidy, and combined Alexa Fluor® 488 and Nanogold® – Fab’ tertiary probe. Specimens were washed with PBS (30 minutes) between each step, then blocked by the addition of 7 % nonfat dried milk to the tertiary antibody solution (original magnification 400 X).

Easily enhanced for electron microscopy, light microscopy, cryo-EM, blots…

Try our precision nanoparticle developers for easily controlled development with low background!

FluoroNanogold™ Combination Labels

Covalently bound, Nanogold® + fluorescent secondary antibodies

Precision meets flexibility

Each secondary antibody / Fab’ includes TWO labels
Covalently bound for stability and long working times:

  1. Fluorescent dye for imaging in Super-Resolution

  2. Nanogold® particles mark your target for TEM, light microscopy and blots!

2-in-1 immunolabeling for Super-Res! 

Simultaneously label for Super-Res AND TEM / light microscopes in a single, standard immunolabeling procedure

Finally– Put your Super-Res images into cellular context!

  • Reveal your fluorescent labeling in traditional microscopes, where you can see the surrounding cell structures!
    • TEM, light microscope, phase contrast, etc.
  • Adaptable to any resolution, for ultimate flexibility in correlative studies
"FNG [FluoroNanogold™] is a probe containing two different markers; it opens the possibility of imaging the same sample at both the optical and the EM level. Thus, it is easy to perform a multimodal investigation, either on different cells or on the same cell visualized by correlative microscopy." Cheutin, T.; Sauvage, C.; Tchélidzé, P, O'Donohue, M. F.; Kaplan, H.; Beorchia, A., and Ploton, D.: Visualizing macromolecules with FluoroNanogold: from photon microscopy to electron tomography. Methods Cell Biol., 79, 559–574 (2007). [This is an entire chapter on FluoroNanogold, providing a detailed and well illustrated write-up of techniques for combined confocal fluorescence microscopic labeling and electron tomography.]

“FNG [FluoroNanogold™] is a probe containing two different markers; it opens the possibility of imaging the same sample at both the optical and the EM level. Thus, it is easy to perform a multimodal investigation, either on different cells or on the same cell visualized by correlative microscopy.”

Cheutin, T.; Sauvage, C.; Tchélidzé, P, O’Donohue, M. F.; Kaplan, H.; Beorchia, A., and Ploton, D.: Visualizing macromolecules with FluoroNanogold: from photon microscopy to electron tomography. Methods Cell Biol., 79, 559–574 (2007). [This is an entire chapter on FluoroNanogold, providing a detailed and well illustrated write-up of techniques for combined confocal fluorescence microscopic labeling and electron tomography.]

By combining gold and fluorescence into one immunoprobe, the same specimen may be imaged using both fluorescence microscopy (e.g., with a confocal microscope) and at the ultrastructural level by electron microscopy.

FluoroNanogold™is now available with Alexa Fluor®* 647, 546, 488 or 594, giving you the benefits of brighter fluorescence, reduced photobleaching, and compatibility with a wider pH range, or in its original formulation with fluorescein as the fluorophore.

Unlike colloidal golds which quench fluorescence, tiny Nanogold® lets the fluorescence shine through. All components are covalently attached to ensure stability and long shelf life. Fab’ antibody fragments are much smaller probes than IgG conjugates, and have shown excellent penetration into cells and nuclei. FluoroNanogold™conjugates are chromatographically purified to eliminate any aggregates, free gold or unattached fluorescent molecules.

  • Unprecedented correlation between fluorescence and EM data.
  • Single labeling procedure means less chance for specimen perturbation.
  • Choice of new fluorophores for brighter fluorescence, lower background and multicolor labeling.
  • Same excellent penetration as found with Nanogold®: much better than 5 and 10 nm colloidal gold probes.
  • FluoroNanogold™ probes are smaller than IgG conjugates (we use Fab’ fragments).
  • Covalent coupling of both labels gives stability and long shelf life.
  • Conjugates are stable and fluorescent at a wide range of pH and ionic strengths.

Applications

  • Correlative fluorescence and electron microscopy 
  • Check your labeling by fluorescence before processing for EM
  • Monitor a dynamic process by fluorescence to determine when to fix and process for EM.
  • Differentiate different targets using different fluorophores.
Immunolocalization of microtubules with Fluorescein FluoroNanogold™-Fab' in the same human monocyte visualized by various microscopies: (A) Fluorescence; (B) Phase; (C) DIC, and (D) Electron Microscopy (with silver enhancement). (Micrographs courtesy of Dr. J. M. Robinson and Dr. D. Vandré, Ohio State University).

Immunolocalization of microtubules with Fluorescein FluoroNanogold™-Fab’ in the same human monocyte visualized by various microscopies: (A) Fluorescence; (B) Phase; (C) DIC, and (D) Electron Microscopy (with silver enhancement). (Micrographs courtesy of Dr. J. M. Robinson and Dr. D. Vandré, Ohio State University).

See your target’s fluorescent label as before

PLUS the Nanogold label for Super-Res, LM, EM and blots

Featured paper:

Sato et al. (2013) used FluoroNanogold™ to explore the mechanism behind cellular dynamics, using correlative microscopy with fluorescence and the new Atmospheric SEM (ASEM).

Dr. Chikara Sato and colleagues with the Atmospheric Scanning Electron Microscope (ASEM).

Dr. Chikara Sato and colleagues with the Atmospheric Scanning Electron Microscope (ASEM).

Fig. 1 Microtubules, visualized by optical microscopy (OM) and atmospheric scanning electron microscopy (ASEM: inverted SEM). COS7 cells were labeled with anti-alpha-tubulin primary antibody followed by Alexa Fluor 488 FluoroNanogold™ secondary antibody (Nanoprobes). Top: Fluorescence microscopy image. Middle: ASEM image of the same cells after gold enhancement by GoldEnhance™ EM (Nanoprobes). Botton: Higher magnification image of the right filopodia. Microtubule rails are clearly observed in the cytoplasm. (Sato et al., 2013)

Fig. 1 Microtubules, visualized by optical microscopy (OM) and atmospheric scanning electron microscopy (ASEM: inverted SEM). COS7 cells were labeled with anti-alpha-tubulin primary antibody followed by Alexa Fluor 488 FluoroNanogold™ secondary antibody (Nanoprobes). Top: Fluorescence microscopy image. Middle: ASEM image of the same cells after gold enhancement by GoldEnhance™ EM (Nanoprobes). Botton: Higher magnification image of the right filopodia. Microtubule rails are clearly observed in the cytoplasm. (Sato et al., 2013)