Sharp size distribution of SPI-Mark™ Colloidal Gold products
While most immuno gold work, with electron microscopy has been done in conjunction with TEM, there have been published some very
exciting results based on the use of SEM as well. For example, there is great interest in using colloidal gold tagged antibodies
for identifying surface antigens on the surfaces of cultured cells. While the precise details of the protocol one would end up
using is very much dependent on the specifics of the samples, we believe that one of the best publications on this topic is the following:
Coller, Barry S., Kutok, J. L., Scudder, L. E., Galanakis, D. K., West, S. M ., Rudomen, G. S., Springer, K. T., "Studies of Activated GPIIb/IIIa
Receptors on the Luminal Surface of Adherent Platelets: Paradoxical Loss of Luminal Receptors When Platelets Adhere to High Density Fibrinogen."
J. Clin. Invest. Vol. 92, pp.2796-2806, 1993.
Everyone has at least some interest in the concentration of the gold colloid
and conjugate in the suspension being purchased. Most of this information
has been gathered on the unconjugated gold probes
but it would be applicable to the conjugates as well. How all this
translates down into what it means in terms of the number of protein
molecules per gold particle, consider these examples for Protein A:
The number of gold particles per ml is another question that is sometimes
asked. We don't have measurements on all gold sizes, but an example is
given for 20 nm gold conjugates:
For an optical density (OD) of 4: 2.8 x 10-12 particles per ml.
Note: Because of some technical difficulties, we are temporarily unable to offer 1 nm gold products, either conjugated or
unconjugated, but the example for 1 nm has been left in the table for illustrative purposes.
The larger the particle the greater the surface area therefore the greater the number of antibodies that can bind. Ultimately, it is
believed that there is some binding of the Fab region and that some binding sites are not going to be available. Some antibodies will
give better sensitivity than others because the amino acids in their Fab fragments don't bind and therefore the Fabs are free. If
sensitivity is poor, it may be worth examining antibodies from other host species, as each will have different characteristics.
Protein A is a lot smaller than IgG, therefore there would be less gold
particles of 1nm gold attached to Protein A, and more Protein A molecules
attached to the larger particles sizes. A 20nm gold particle would have
something like 150 Protein A molecules compared to the 48 IgG's.
Quite a bit of time, effort, and energy is spent characterizing such issues for the SPI-Mark Gold Probes, so if you have additional questions, let us
know, but with the caveat that what we tell you about the SPI-Mark brand of colloidal gold probe suspensions would not be directly applicable to other brands.
Questions often times come up about what should be the "correct color". In
general, the SPI-Mark Colloidal Gold products, like all other colloidal gold
products (to our knowledge) are that deep "Cabernet Sauvignon" red or almost
purple color except for the SPI-Mark 2 nm gold products. Both
are pale straw in color, and look brown when concentrated x10. If one ends
up with a water white clear solution and they don't now if there is any gold
present or not, then the conclusive "test" is to blot 1µl of each onto a
nitrocellulose membrane filter and silver enhancing.
If the clear solutions don't enhance, then there are no gold particles present.