The Muta-ChromoPlate provides a clear colour endpoint. Reagents, cultures and other consumable components are supplied ready-to-use in a non-specialized laboratory. The Muta-ChromoPlate kit is based on the most generally used and bacterial reverse mutation test, known as the Ames Test (Ames et al., 1975 Mutation Research 31:347)
The test employs a mutant strain, or several strains, of Salmonella typhimurium, carrying mutation(s) in the operon coding for histidine biosynthesis. When these bacteria are exposed to mutagenic agents, under certain conditions, reverse mutation from amino acid (histidine) auxotrophy to prototrophy occurs.
Traditionally, reverse-mutation assays have been performed using agar plates. An alternate assay performed entirely in liquid culture is the 'Fluctuation Test' based on multiple yes/no colour endpoints (Hubbard, S.A et al., 1994, pp. 141-160, in Kilbey et al. (Eds.), Handbook of Mutagenicity Testing (2nd Ed,.) Elsevier Sciences, NY. This test principle is being applied in the Muta-ChromoPlate test kit.
The Muta-ChromoPlate Kit is generally more sensitive (up to 10 times) than the pour-plate assay, because it allows testing of higher concentrations of sample (up to 75% v/v). The assay procedure is simple and requires minimal training. Consumable components are provided with ready-to-use and step-by-step instructions. "Instructions for Use" are provided with the basic kit. The only equipment required are a 37 degree Celsius incubator and a single and a multi-channel micropipettor.
What New with EBPI's Ames Strains? EBPI has developed a new line of Ames Express bacteiral strains that include an internal bio-activation based on human recombinante liver enzymes. EBPI visit www.Biotoxicity.com to learn more about this new exciting product launch.
S9 Activation Enzymes S9 is a crude liver enzyme extract that can, under certain conditions, convert materials without any genotoxic activity to active genotoxic entities. The chemical process involved is probably different for different materials. In addition, the lifetime of the activated moieties is extremely variable: some may be extremely short-lived. This is the reason for incubating the S-9 with the bacteria and the tested material at the same time. |