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Isolation detergents

Density gradient centrifugation to isolate detergent-resistant membranes... [Pg.42]

Figure 9. Typical fluorescence signals obtained from a suspension of isolated rat cardiac myocytes after the application of maitotoxin (MTX). The arrow indicates the addition of MTX (10 g/mL), a detergent Emulgen 810 (1%), which frees all vesicular Ca , or EGTA (3.5 mM), a chelator that removes all free Ca in the cuvette. The intensity of Quin 2 fluorescence is expressed in arbitrary units. (Reproduced with permission from Ref. 20. Copyright 1987 Elsevier)... Figure 9. Typical fluorescence signals obtained from a suspension of isolated rat cardiac myocytes after the application of maitotoxin (MTX). The arrow indicates the addition of MTX (10 g/mL), a detergent Emulgen 810 (1%), which frees all vesicular Ca , or EGTA (3.5 mM), a chelator that removes all free Ca in the cuvette. The intensity of Quin 2 fluorescence is expressed in arbitrary units. (Reproduced with permission from Ref. 20. Copyright 1987 Elsevier)...
Hospital isolates of Serratia marcescens may be highly resistant to ehlorhexidine, hexachlorophane liquid soaps and detergent creams. The outer membrane probably determines resistance to biocides. [Pg.268]

Sample preparation used to extract proteins from cells prior to analysis is an important step that can have an effect on the accuracy and reproducibility of the results. Proteins isolated from bacterial cells will have co-extracted contaminants such as lipids, polysaccharides, and nucleic acids. In addition various organic salts, buffers, detergents, surfactants, and preservatives may have been added to aid in protein extraction or to retain enzymatic or biological activity of the proteins. The presence of these extraneous materials can significantly impede or affect the reproducibility of analysis if they are not removed prior to analysis. [Pg.206]

FIGURE 10.12 The mole ratio of carotenoid/phospholipid and carotenoid/total lipid (phospholipid + cholesterol) in raft domain (detergent-resistant membrane, DRM) and bulk domain (detergent-soluble membrane, DSM) isolated from membranes made of raft-forming mixture (equimolar ternary mixture of dioleoyl-PC (DOPC)/sphingomyelin/cholesterol) with 1 mol% lutein (LUT), zeaxanthin (ZEA), P-cryptoxanthin (P-CXT), or P-carotene (P-CAR). [Pg.205]

The isolated cells may be lysed using standard mechanical or detergent methods and the biotinylated cell-surface proteins analyzed or isolated using (strept)avidin reagents. [Pg.520]

The structure and roles of membrane microdomains (rafts) in cell membranes are under intensive study but many aspects are still unresolved. Unlike in synthetic bilayers (Fig. 2-2), no way has been found to directly visualize rafts in biomembranes [22]. Many investigators operationally define raft components as those membrane lipids and proteins (a) that remain insoluble after extraction with cold 1% Triton X-100 detergent, (b) that are recovered as a low density band that can be isolated by flotation centrifugation and (c) whose presence in this fraction should be reduced by cholesterol depletion. [Pg.28]

The sodium and calcium pumps can be isolated to near purity and still exhibit most of the biochemical properties of the native pump. Some kinetic properties of these pumps in native membranes are altered or disappear as membrane preparations are purified. For example, when measured in intact membranes, the time-dependencies of phosphorylation and dephosphorylation of the pump catalytic sites exhibit biphasic fast to slow rate transition this characteristic progressively disappears as the membranes are treated with mild detergents. One suggested explanation is that, as the pumps begin to cycle, the catalytic subunits associate into higher oligomers that may permit more efficient transfer of the energy from ATP into the ion transport process [29, 30], Some structural evidence indicates that Na,K pumps exist in cell membranes as multimers of (a 3)2 [31]. [Pg.82]

Cell fractionation procedures were fundamental to the biochemical identification of steroid and thyroid hormone receptors in brain as well as in other tissues. Isolation of highly purified cell nuclei from small amounts of tissue from discrete brain regions generally is accomplished with the aid of a nonionic detergent, such as Triton X-100 [7],... [Pg.849]

Conductivity sensors are most commonly used for safety purposes in household appliances. Presence and absence of washing liquor, detergency, and water softener can be easily measured and proper operation ensured [71]. The various applications mainly differ by their design of electrode geometry and methods for electrical measurement. Due to the close relation between ionic conductivity and water hardness, the automatic water softener in an automatic dishwasher can be controlled by a conductivity sensor [72]. To isolate the transmission of the measured value from the process controller, the conductivity sensor could incorporate an opto-electronical coupling [73]. Thus, protective insulation of the electrodes in a washer-dryer could be ensured. [Pg.107]

After use, all containers should be drained and rinsed several times with a solution of water, detergent, and lye ( bury rinse solution deeply in an isolated location with 18 inches [7 cm] of cover ) the empty container should be punctured and crushed to prevent reuse. [Pg.1070]


See other pages where Isolation detergents is mentioned: [Pg.42]    [Pg.23]    [Pg.274]    [Pg.42]    [Pg.23]    [Pg.274]    [Pg.459]    [Pg.206]    [Pg.130]    [Pg.173]    [Pg.295]    [Pg.503]    [Pg.225]    [Pg.181]    [Pg.440]    [Pg.419]    [Pg.208]    [Pg.177]    [Pg.322]    [Pg.125]    [Pg.59]    [Pg.278]    [Pg.109]    [Pg.121]    [Pg.45]    [Pg.121]    [Pg.321]    [Pg.73]    [Pg.149]    [Pg.890]    [Pg.585]    [Pg.128]    [Pg.196]    [Pg.315]    [Pg.335]    [Pg.967]    [Pg.90]    [Pg.339]    [Pg.362]    [Pg.151]    [Pg.576]    [Pg.784]    [Pg.234]   
See also in sourсe #XX -- [ Pg.57 ]




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