Marker, generation

The idea here is deceptive in its apparent simplicity physical markers generate race consciousness, and race consciousness in its turn influences social relations. The content of race, then—the specific set of traits that constitutes blackness, for instance—is secondary to the social relations created and maintained by the consciousness that such traits stir within both those who possess them and those who do not. 

Py-GC/MS can be applied for both qualitative and quantitative purposes. One typical use of quantitative analysis using pyrolysis is the determination of the amount of a specific polymer in a given complex matrix, such as a composite material, inorganic matrix, etc. Since solubilization is frequently a very difficult task for these materials, pyrolysis can provide quantitative information based on the level of the polymer marker generated by the thermal decomposition. Calibration is typically necessary in these situations, and similarly to other analytical procedures this can be achieved using a standard addition type procedure (see e.g. [17]) or a calibration with known amounts of polymer in a similar or identical matrix. Another case where the quantitation can be necessary is the determination of the amount of a comonomer in a copolymer sample. Successful quantitation by Py-GC/MS is reported in literature for various copolymers [25-39], etc. 

The difference between these two equations dictates that there will be an error if the coinjection equation is used for a delayed injection marker. Table 19.2 shows several examples and the magnitude of the errors generated. 

TABLE 19.2 Errors Generated by Improper Flow Marker Correction... 

Cellular therapies in transplantation and cancer are based on specific cells separated or sorted from human blood, bone marrow, or cord blood by means of their specific cell surface markers or cell differentiation antigens, e.g., CD3, CD4, CD8, CD 14, CD 19, and CD34. For example, the CD34+ stem cells, especially those derived from human embryos, have the capacity to differentiate in culture to generate different somatic cells, e.g., liver cells, heart cells, neurons, etc. This exploding field of research is now termed regenerative medicine. 

An important additional pathway is indicated in reactions I and II of Figure 47-9. This involves enzymes destined for lysosomes. Such enzymes are targeted to the lysosomes by a specific chemical marker. In reaction I, a residue of GIcNAc-1-P is added to carbon 6 of one or more specific Man residues of these enzymes. The reaction is catalyzed by a GIcNAc phosphotransferase, which uses UDP-GlcNAc as the donor and generates UMP as the other product ... 

Marker, H.S., Weiss, C., Silides, D.J., and Cohen, G. (1981). Coupling of dopamine oxidation (monoamine oxidase activity) to glutathione oxidation via the generation of hydrogen peroxide in rat brain homogenates. J. Neurochem. 36, 589-593. 

By far the most widely measured marker of hemostatic activation is D-dimer, which is a product formed by the action of plasmin on cross-linked fibrin (95). D-dimer levels in plasma are generally elevated in DIC. The consumption of platelets and coagulation proteins as a result of thrombin generation leads to the deposition of fibrin thrombi at multiple organ sites. This triggers fibrinolysis with an increase in the formation of fibrin degradation products, which can cause bleeding at multiple sites. Because DIC can have a variety of causes and may coexist with systemic fibrinolysis, such as in pulmonary embolism or deep vein thrombosis, the d-Dimer test is not specific for DIC (95). 

Figure 4. DDC (A), serotonin (B), and tyrosine hydroxylase (C) immunore-activity in the posterior region of a wild-type Drosophila ventral ganglion. Tyrosine hydroxylase (TH) encodes the rate-limiting step in dopamine biosynthesis and is a marker for dopamine cells. B and C are the same CNS assayed for both serotonin and TH. M, medial dopamine neurons VL, ventrolateral serotonin neurons DL, dorsolateral dopamine neurons. Short unmarked arrows in C show vacuolated cells that do not contain DDC immunoreactivity. The immunoreactivity in these cells may represent a nonspecific cross-reactivity of the rat TH antibody. The length bar in A is 50 pM. The images are confocal projections generated on a Molecular Dynamics-2000 confocal laser scanning microscope.

---