Gold is the new silver! Silver enhancement has long been used by microscopists to better visualize gold labeling, especially when using small gold particles. With GoldEnhance™, gold ions are specifically deposited around the gold nanoparticle, growing it in size, and offering several advantages over silver.
For TEM, the 1.4 nm Nanogold® can be enlarged to 3-20 nm for clear visiblility, even at low magnifications. Using an initial small gold immunoprobe allows better penetration into tissues (up to 40 microns!) and better labeling of antigens. Then gold enhancement makes everything clearly visible.
The development time can be extended to deposit more gold and make the signal visible by bright field (or reflection) light microscopy. With a little more development time, the signal can be seen by the naked eye, and can be used with dot blots or Westerns.
May safely be used before osmium tetroxide staining (silver is dissolved by the oxidizing agent O4; gold is stable)
Lower backgrounds than silver in many cases; autonucleation minimal even after 1-2 hours
For SEM, gold gives a much better backscatter signal than silver
Compatible with physiological buffers (silver precipitates with chloride ion, as in PBS buffer; gold does not)
Reaction is less pH senstitive than silver, and GoldEnhance™ is near neutral for best structural preservation of biological samples (many silver enhancers have a pH of 3-4)
Excellent shelf life
Low viscosity for easy and accurate mixing of components
Our customers report superb results in their labs, with real improvement over silver enhancement
for light microscopy, electron microscopy and blots.
Much better than enzymatic detection for LM!
Direct detection:
Light micrographs of formalin-fixed serial sections of cervical carcinoma, in situ hybridized for HPV-16/18 using a biotinylated probe (Pathogene-HPV kit, Enzo)
(Micrographs courtesy of Prof. G. W. Hacker. Medical Research Coordination Center, University of Salzburg, Austria)
Deposit metallic gold to enlarge ultrasmall gold nanoparticles for EM - Use it with Nanogold®!
Slow enhancement for an easy control of particle size
Great for SEM: Gold gives a much better backscatter signal than silver
Low background - No autonucleation for 40 minutes
Neutral pH for best ultrastructural preservation
Permanent staining: does not fade
Resistant to osmium tetroxide etching: may safely be used before osmium tetroxide staining with no need for gold toning or other protective treatments. Gold is stable in the oxidizing agent OsO4; silver would dissolve.
Compatible with physiological buffers and other halide solutions --these would precipitate silver.
Can be used for specimens on metal surfaces (e.g. cell culture substrates)
High density of enlarged particles for clear imaging.
Resistant to osmium tetroxide etching: may safely be used before osmium tetroxide staining with no need for gold toning or other protective treatments (silver is dissolved by the oxidizing agent OsO4; gold is stable).
for SEM, gold gives a much better backscatter signal than silver.
Custom conjugation is also available, of Nanogold®, FluoroNanogold, undecagold
or colloidal gold to primary antibodies, peptides, small molecules, or other molecules.
International orders:Our regional distributors can provide expedited customs processing and delivery.