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Content analysis

Please write a short definition regarding how you would define social justice. [Pg.414]

What is the relationship between ethics and social justice  [Pg.414]

What are some of the issues facing engineers regarding social justice  [Pg.414]

How and where do you address social justice in your courses In the program Please provide examples. [Pg.414]

Do you think it is important to integrate social justice in the engineering program Why or why not  [Pg.414]


Halogen, sulphur, nitrogen content Ash content Analysis of ash Organic content by BOD, COD, PV or total carbon methods completed... [Pg.542]

These techniques help in providing the following information specific heat, enthalpy changes, heat of transformation, crystallinity, melting behavior, evaporation, sublimation, glass transition, thermal decomposition, depolymerization, thermal stability, content analysis, chemical reactions/polymerization linear expansion, coefficient, and Young s modulus, etc. [Pg.655]

A content analysis of 11 general chemistry laboratory manuals was carried out by Domin (1999a) and concluded that the majority require the learners to operate predominantly at the three lower cognitive levels of Bloom s taxonomy (knowledge, comprehension and application), leaving out the three higher levels of analysis, synthesis and evaluation. [Pg.112]

Domin, D. S. (1999a). A content analysis of general chemistry laboratory manuals for evidence of higher-order cognitive tasks. Journal of Chemical Education, 76, 109-112. [Pg.130]

Sanger, M. J., Rhelps, A. J. (2007). What are students thinking when they pick their answer A content analysis of students explanations of gas properties. Journal of Chemical Education, 84(5), 870-874. [Pg.190]

Dry ashing procedures for elemental and ash content analysis fall into the following categories ... [Pg.593]

We use gel content analysis to determine the weight fraction of a crosslinked polymer that is bound into an insoluble network. We immerse a stainless steel mesh basket containing a known weight of the crosslinked polymer in a suitable solvent (which may be heated to facilitate dissolution). If necessary, we can slice or grind the sample to increase its surface area. After 24 hours or more, we remove the basket from the solvent and dry it to constant weight. We calculate the gel content from Eq. 5.6. [Pg.118]

The metal content analysis of the samples was effected by Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES Varian Liberty II Instrument) after microwaves assisted mineralisation in hydrofluoric/hydrochloric acid mixture. Ultraviolet and visible diffuse reflectance spectroscopy (UV-Vis DRS) was carried out in the 200-900 nm range with a Lambda 40 Perkin Elmer spectrophotometer with a BaS04 reflection sphere. HF was used as a reference. Data processing was carried out with Microcal Origin 7.1 software. [Pg.286]

Kitchen scales, mixers or refrigerators could be equipped with food content analysis systems that would not only determine the weight e.g. of fruit or vegetable, but also provide data on freshness and nutritional information, e. g. about en-... [Pg.224]

See also Epoxy coatings Epoxy chalcone, 10 450 12,13-Epoxy-cis-9-octadecenoic (vernolic) acid, physical properties, 5 35t Epoxy coatings, 10 436 450 17 845. See also Epoxy can coatings for corrosion protection, 7 199 markets for, 10 442-449 performance of, 10 423 waterborne, 10 439 Epoxy composites, 10 450, 451 Epoxy compounds, photoinitiated polymerization of, 23 716 Epoxy content analysis, 10 385 Epoxy cresol novolac (ECN) resins, 10 367, 369... [Pg.324]

Flow cytometry (FCM) is widely used for exploring mechanism of action of compounds that compromise proliferation since it is rapid, accurate and usable for any cellular context [5], In this chapter we want to point out technical and strategic aspects of use of FCM for cell cycle studies of a putative anticancer agent. As an example we used Edotecarin, a topi inhibitor, firstly evaluating proliferation outcome and classical DNA content analysis by propidium iodide, and then since the compound treatment produced cell cycle perturbation difficult to interprete, a two-parametric analysis by 5-bromo-deoxyuridine (BrdU) was applied for separating cell cycle phases. Moreover we put our efforts into identifing specific cell cycle arrest not easily demonstrable by previously described methods, through the use of in vitro kinetics ( pulse and chase ). Finally, in vivo assessment of efficacy and biomarkers modulation after treatment was analyzed. [Pg.76]

Unfortunately monoparametric DNA content analysis by PI is not able to discriminate from different cell cycle phases, and as exemplified in Figure 4, monoparametric analysis by PI show its limitations, since this flow cytometric assay does not display any details S-phase activities after drug treatments. At this point, cells can be arrested in a specific cell phase (eg. Gi or G2/M) and obviously a decrease of S-phase is observed. [Pg.81]

Nevertheless, drugs effects can compete with BrdU uptake in DNA synthesis machinery in case of antimetabolites treatments [20] or after lacking ability to incorporate following DNA damages accumulation or in case of presence of apoptotic cells. Moreover, when cells are delayed between Gi to S (early S, ES) or S to G2/M (late S, LS), only DNA content analysis make accurate quantifications impossible [25],... [Pg.82]

Monoparametric DNA Analysis Fixed cells were stained with PI 25 pg/niL, RNase 5 pg/mL, Nonidet P 40 0.125 pg/mL. Cells were kept at RT for 60 in the dark and were analyzed by BD FACSCalibur flow cytometer. Aggregates were gating out by DDM papameters and DNA content analysis was performed in >10,000-gated cells. DNA histograms were analyzed using ModFit LT . [Pg.94]

To elucidate some enzymatic characteristics of the isolated laccases I, II, and III, substrate specificities for several simple phenols, electrophoresis patterns, ultraviolet spectra, electron spin resonance spectra, copper content, and immunological similarities were investigated. Tyrosine, tannic acid, g c acid, hydroquinone, catechol, pyrogallol, p-cresol, homocatechol, a-naphthol, -naphthol, p-phenylenediamine, and p-benzoquinone as substrates. No differences in the specificities of these substrates was found. The UV spectra for the laccases under stucfy are shown in Figure 4. Laccase III displays three adsorption bands (280, 405, and 600nm), laccase II shows one band 280nm), and laccase I shows two bands (280 and 405 nm). These data appear to indicate differences in chemical structure. The results of the copper content analysis (10) and two-dimensional electrophoresis also indicate that these fractions are completely different proteins (10), Therefore, we may expect differences in substrate specificities between the three laccase fractions for more lignin-like substrates, yet no difference for some simple phenolic substrates. [Pg.208]

Key words High content analysis, Protein fragment complementation. Protein-protein interactions. [Pg.179]

There are a number of stains to label the nucleus for the purpose of detection in high content analysis. We use DRAQ5 to label not only the nuclei but also the cytosol to a lesser extent. With thresholds properly adjusted, imaging software can detect the nuclei and cytosol in the same channel in two consecutive steps with just one staining. [Pg.184]

O Brien, P.J. (2008) Chapter 13 High content analysis of sublethal cytotoxicity in human HepG2 hepatocytes for assessing potential and mechanism for chemical and drug-induced human toxicity, in High Content Screening Science, Techniques and Applications (ed. S.A. Haney), John Wiley Sons, Hoboken, NJ,... [Pg.343]

O Brien, P.J. and Domingos, M.C. (2009) Use of high content analysis in toxicologic clinical pathology for identification and monitoring of translational safety biomarkers. American Drug Discovery... [Pg.343]

Reactivity ratios between acrylated lignin model compound (Fig. 2), defined as Mi, with either MM A or S, defined as M2, were determined experimentally in accordance with standard procedures (15). These involve mixing two different vinyl monomers in various molar ratios with catalyst (i.e., benzoyl peroxide) and solvent, heating the mixture to achieve polymerization, and recovering the polymer by the addition of non-solvent, and centrifugation. The respective molar monomer fractions of the copolymer were determined by UV-spectroscopy in the cases where MMA served as M2, and by methoxyl content analysis in those cases in which S was the M2-species. The results were subjected to numerical treatments according to the established relationships of Kelen-Tiidos (17) and Yezrielev-Brokhina-Roskin (YBR) (18), and this is described elsewhere (15). [Pg.520]

Water crystallization in frozen whippable emulsions such as ice cream or aerated desserts, may be analysed by the NMR technique similar to that described for solid fat content analysis. Again, this technique is best used for only relative studies on the effects of ingredient composition on freezing/melting behaviour. [Pg.83]

In terms of our typology of mysticism, ideally the most "complete" mystical experience should have demonstrated the phenomena of all the categories in a maximal way. The evidence (particularly from the content analysis and also supported by impressions from the interviews) showed that such... [Pg.156]

Proteomics in parasitic flatworms can be completed on intracellular fractions (e.g. microsomal or cytosol) or at the host-interface on excretory-secretory (ES) products. ES analysis can be completed during in vitro culture or in vivo by, for example, bile or gut content analysis. In all cases, a rapid and careful preparation is vital to prevent altered pro-teomic profiles due to stress responses (upreg-ulation of heat shock proteins) and action of proteases. Parasitic flatworms are best extracted from fresh host material, washed with a buffered saline solution at approximately the host s body temperature. In F. hepatica, for example, this will allow regurgitation of gut contents to remove digested material from, and removal of host material adherent to the outer surfaces of the parasite (Jefferies et al., 2001), both of which can subsequently complicate separation and identification. [Pg.329]

The optimal moisture content of the dried granulation needs to be determined. High moisture content can result in (1) tablet picking or sticking to tablet punch surfaces and (2) poor chemical stability as a result of hydrolysis. An overdried granulation could result in poor hardness and friability. Moisture content analysis can he performed using the conventional loss-on-drying techniques or such state-of-the-art techniques as near infrared (NIR) spectroscopy. [Pg.215]

Konemann, S., Schuck, A., Malath, J., Rupek, T., Horn, K., Baumann, M., Vormoor, J., Rube, C., and Willich, N. 2000. Cell heterogeneity and subpopulations in solid tumors characterized by simultaneous immunophenotyping and DNA content analysis. Cytometry 41 172-177. [Pg.326]


See other pages where Content analysis is mentioned: [Pg.176]    [Pg.364]    [Pg.291]    [Pg.96]    [Pg.231]    [Pg.118]    [Pg.407]    [Pg.83]    [Pg.111]    [Pg.105]    [Pg.179]    [Pg.179]    [Pg.325]    [Pg.327]    [Pg.204]    [Pg.550]    [Pg.108]    [Pg.760]    [Pg.122]    [Pg.532]    [Pg.398]    [Pg.155]   
See also in sourсe #XX -- [ Pg.65 , Pg.70 , Pg.71 , Pg.83 ]

See also in sourсe #XX -- [ Pg.234 ]




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Analysis Iron content

Analysis ammonia content

Analysis bacterial content

Analysis manganese content

Analysis of Chemical Information Content Using Shannon Entropy

Analysis of Metal Salt Content Dissolved in Aerosol Solvent(s)

Analysis of Metal Spiked Oil Blends Using High Pressure Oxygen Combustion for Metals Content

Analysis of Old Lubricating Oil for Total Metal Content Using a Slurry Method with Internal Standard

Analysis of Organs and Organ Content

Analysis of Plastics, Fibres and Textiles for Metals Content Using ICP-OES

Analysis sulfate content

Analysis sulfide content

Consciousness content analysis

Content ranges, trace analysis

Contents 14 Quantitative image analysis

Contents 9 Analysis overview

Contents Break-Even Analysis

Gastric contents analysis

Gel content analysis

Genome analysis gene content

High content analysis

High content analysis assays

High content screening analysis

High content screening microscopy analysis

Information Content of Quantitative Analysis

Information content analysis

Milk analysis water content

Near-infrared protein content analysis

Thermal analysis water content measurement

Thermal gravimetric analysis content

Uranium Content Analysis in Other Bioassays

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