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D diffusion can give much larger mass flux to the surface than does 1-D diffusion.

D display mode for a diode-array detector .

D display models for tensile, shear, and mixed-mode cracks.

D distribution of cadmium and mercury

D Dq vs. time, impregnated catalysts

D eatment of compound 19 with an activatedphosphorylethanolamine derivative.

D electrophoretic separations of laser capture microdissected human cardiac tissue.

D ependence of the reactive force of a superheated-water jet on the initial pressure corresponding to the saturation line. Solid line - calculation for the hydraulic regime of outflow of a one-phase liquid.

D ESRI at 298 K of a phantom consisting of two parallel capillary tubes separated by 3 mm and filled with a solution of TEMPO in benzene, . Redrawn from Ref 55, with permission.

D ester degradation with time in presence of

D ester degradation with time. , amount in

D ethyl acetate-glacial acetic acid-formic acid-water 100 11

D ethyl acetate-methanol-water 100

D Expression of astrocyte markers in adult mouse DG. A Staining for S100 J demonstrates the lower density of positive cells in DGL as compared to neighboring DG layers. However, no difference could be seen among the molecular layer . Scale bar 50 pm

D fferent mechanisms of dynamic quenching

D Fibonacci sequence. Moving downwards corresponds to an inflation of the self-similar chains, and moving upwards corresponds to a deflation

D fits to sample van der Waals data, illustrat-

D for similar plots of dtpjdy and dipjdz for the first n—n excitation of ethylene

D from Brookhaven Symposium Biology, by J. Gall, 1955

D from Escherichia coli and Salmonella typhimurium by R. M. Macnab, , 1987

D FT-IR images based on the integrated v for deuteration time t Omin and 193 min. The dashed line indicates the NH ND exchange front.

D FVM grid with a control volume embracing a node P.

D g values for the bilayers composed of the 3Rg thick d-PS spin cast films with the different scaled film thicknesses by Rg of the h-PS polymer. Figure reproduced from Ref. with permission from American Chemical

D Gel Electrophoresis of in vitro Translated Soybean Epicotyl mRNA. Experimental conditions are as described in

D Gel Electrophoresis of in vitro Translated Soybean Hypocotyl mRNA. Numbers to the left indicate migration of molecular weight markers . The separating gel was 12 polyacrylamide. Numbered arrows indicate polypeptides that are up-regulated by BR while lettered arrows show polypeptides that are down-regulated in response to BR. Other experimental details are described in the text. A hypocotyl sections auxin-depleted for 2 hours followed by buffer treatment for 2 hours A as in A with 340 nM BR replacing buffer treatment.



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