Identification marker

Hartmann, U. (1990). Magnetic force microscopy. Advanced Materials, 2,550-2. Hasegawa, R. (1991). Glassy alloy identification marker. Journal of Applied Physics, 69, 5025-6. 

To summarize, the total gamma ray measurements are used for real-time correlation, lithology identification, depth marker and kick-off point selection. 

Finally, it is worth mentioning that tryptase levels do not differentiate between immunologic and non-immimological mast cell activation and do not contribute to the identification of the cause of the anaphylactic reaction. To date, very few mediators [10] apart from histamine and tryptase have been investigated as markers for anaphylaxis. Recent studies also include other mediators that we will only examine briefly. A more extensive review can be found elsewhere [2,11]. 

Analysis in diverse lines can facilitate identification of useful alleles that control expression of enzymes upstream of the carotenoid pathway, a feature that would not be evident from conventional end-product screening of breeding lines. Moreover, this characterization sets the stage for marker-assisted selection of superior endogenous alleles and facilitates selection of introduced transgenes that may be necessary to supplement the genotypic contribution required for a particular plant chemical outcome. 

The Use of PLC for Isolation and Identification of Unknown Compounds from the Frankincense Resin (Olibanum) Strategies for Finding Marker Substances... 

The identification and quantification of potentially cytotoxic carbonyl compounds (e.g. aldehydes such as pentanal, hexanal, traw-2-octenal and 4-hydroxy-/mAW-2-nonenal, and ketones such as propan- and hexan-2-ones) also serves as a useful marker of the oxidative deterioration of PUFAs in isolated biological samples and chemical model systems. One method developed utilizes HPLC coupled with spectrophotometric detection and involves precolumn derivatization of peroxidized PUFA-derived aldehydes and alternative carbonyl compounds with 2,4-DNPH followed by separation of the resulting chromophoric 2,4-dinitrophenylhydrazones on a reversed-phase column and spectrophotometric detection at a wavelength of378 nm. This method has a relatively high level of sensitivity, and has been successfully applied to the analysis of such products in rat hepatocytes and rat liver microsomal suspensions stimulated with carbon tetrachloride or ADP-iron complexes (Poli etui., 1985). 

Martos, I., Ferreres, F., Francisco, A., and Tomas-Barberan, F. A. (2000a). Identification of flavonoid markers for the botanical origin of eucalyptus honey. /. Agric. Food Chem. 48, 1498-1502. 

Figure 7.7 Separation of ethynyl estrogens on silica gel 60 HPTLC plates using two 15-min developments in the solvent system hexane-chloroform-carbon tetrachloride-ethanol (7 18 22 1 v/v). Identification O methyl green (lane marker) 1 17a-ethynylestradiol ...

Ralph, J. Kim, H. Lu, F. Grabber, J. H. Boerjan, W. Leple, J.-C. Berrio Sierra, J. Mir Derikvand, M. Jouanin, L. Lapierre, C. Identification of the structure and origin of a thioacidolysis marker compound for ferulic acid incorporation into angiosperm lignins (and an indicator for cinnamoyl-CoA reductase deficiency). Plant J. 2008, 53, 368-379. 

Popik W, Alee TM. CD4 receptor localized to non-raft membrane microdomains supports HIV-1 entry. Identification of a novel raft localization marker in CD4. J Biol Chem 2004 279(1) 704-712. 

CHEMICAL MARKERS FOR PROTEIN-BASED IDENTIFICATION OR BIODETECTION... 

This result is important to fully understanding the biochemical and ultra-structural origin of peaks and the physiological basis for variation. It not only helps in designing the analytical strategy (e.g., in selection of cleanup columns) but, more important, in making a decision on whether the marker should be used for strain or species identification or for biodetection. For example, there are a number of low-molecular weight peptides (1500-8000 kDa) present in... 

B. anthracis and related species.41,44 6 Some of these peaks have been identified (e.g., as small acid soluble spore proteins and cyclic lipopeptides), but others remain uncharacterized. There is no agreement among different laboratories as to which markers are suitable for chemotaxonomic differentiata-tion of species (i.e., are consistently found in one species versus another) or for strain identification (i.e., are reproducibly found in one strain but not another). Further, although it might be anticipated that surface proteins can be preferentially ionized or extracted, the ultra-structural origin of some peptides within the cell is not always clear. 

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