Substrate chromogenic

Goebel and Avery J Exptl Medicine 50 521 7929 Snyder and Link J Am Chem Soc 75 1758.] chromogenic substrate for P-galactosidases [Buoncore et al. J Appl Biochem 2 390 1980]. 

Identification by nuclear magnetic 19A Chromogenic substrate assay... 

The CTAD additive mixture has found application in the monitoring of heparin therapy by either the chromogenic substrate assay or the APTT and in the measurement of platelet markers such as P-selectin (CD62) by flow cytometry (108, 109). 

Muftic, M. K. Application of chromogenic substrates to the determination of peptidases in mycobacteria. Folia Microbiol. (Prague, Czech Republic) 1967,12, 500-507. 

Levine MN, Lavis LD, Raines RT (2008) Trimethyl lock a stable chromogenic substrate for esterases. Molecules 13 204-211... 

Alkaline phosphatase is an enzyme represented by various isoforms in many tissues such as liver, bone, intestine, placenta, some tumors and in leukocytes. Addition of 1 mM levamisole to the chromogen/substrate will inhibit endogenous alkaline phosphatase activity, with the exception of the intestinal isoform. If necessary, this can be blocked with a weak acid wash, such as 0.03 0.5 N HC1 or 1 M citric acid. 

Niewola et al. [183, 185] have described a rapid, convenient and accurate method, based upon an enzyme-based immunosorbent assay (ELISA) for the determination of Paraquat residues in soil. Polystyrene plates, coated with paraquat-keyhole limpet haemocyanin (KLH) conjugate, are incubated with the test samples and a known amount of monoclonal antibody. Residual antibody that has not reacted with free Paraquat in the sample combines with paraquat-KLH on the plate. The determination of the fixed antibody is achieved by the addition of peroxidase labelled rabbit antimouse immunoglobulin G followed by reaction with a chromogenic substrate. The enzyme activity of the solid phase is determined from the absorbance measurements, which are inversely proportional to the concentration of Paraquat. The method shows high specificity and correlates well with the traditional ion exchange-spectrophotometric method for the determination of Paraquat [178]. 

In addition to the many enzyme systems available, there are with each a series of chromogenic substrate solutions that can be used to create different colors and locations of reaction products. For the peroxidase system, there are numerous oxidizable compounds that precipitate as a permanent color. The most common and still widely used is 3,3 diaminobenzidine tetrahydro-chloride (DAB). This compound precipitates to a golden brown color when in solution with peroxidase and hydrogen peroxide. This brown color has many subtleties and readily stands out in a tissue section. With practice, it is possible to differentiate specific from nonspecific staining patterns just by examining the characteristics of the precipitated pigment. This material is also insoluble in alcohol and xylene, and therefore the tissue may be routinely dehydrated and cleared without loss of chromogen. 

In this technique, once the specimens have been prepared (see Chapters 8-13), the antibody solution at the appropriate dilution is applied. Following 30 min of incubation, extensive washing is done before incubation with the chromogen. Washes totaling 30 min should be performed. The antigen is then detected by incubation in the chromogenic substrate solution. 

The wide range of chromogenic-substrate systems available allows one to obtain excellent color contrast for double/multiple antigen detection. Chromo-genie reactions resulting in black (IGSS), yellow-brown (IPO/DAB), red-brown (IPO/AEC), blue (lAP/Fast Blue, or 5-bromo-4-chloro-3-indolyl phosphate/ nitroblue tetrazolium [BCIP-NBT]), and purple (lAP/Fast Red or New Fuchsin) can be used in different combinations (see Chapter 23). For development of these products, the following protocols are provided (see Note 16). 

Toxi-Chromotest is a commercial toxicity assay that is based on the assessment of the inhibition of (3-galactosidase activity, measured using a chromogenic substrate and a colorimeter. A mutant strain of Escherichia coli is revitalized from a lyophilized state prior to the test [39]. The principle of the MetSoil test is similar to that of the Toxi-Chromotest . 

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