scholarly journals Determination of Ca2+ concentration in cells using Ca electrode.

1985 ◽  
Vol 25 (4) ◽  
pp. 168-173 ◽  
Author(s):  
YASUNOBU OKADA
Keyword(s):  
In Cells

Utilization of Labelled ‘Myleran’ for the Determination of the Size of DNA Molecules in Cells

Nature ◽  
1964 ◽  
Vol 203 (4947) ◽  
pp. 865-867 ◽  
Author(s):  
W. G. VERLY ◽  
A. PETITPAS-DEWANDRE
Keyword(s):  
Dna Molecules ◽  
In Cells

Determination of topological structure of ARL6ip1 in cells: Identification of the essential binding region of ARL6ip1 for conophylline

FEBS Letters ◽  
2013 ◽  
Vol 587 (22) ◽  
pp. 3656-3660 ◽  
Author(s):  
Masahiro Kuroda ◽  
Shintaro Funasaki ◽  
Tsuyoshi Saitoh ◽  
Yukiko Sasazawa ◽  
Shigeru Nishiyama ◽  
...  
Keyword(s):  
Topological Structure ◽  
Binding Region ◽  
In Cells

scholarly journals The current distribution in an electrochemical cell. Part VII. Concluding remarks

2002 ◽  
Vol 67 (4) ◽  
pp. 273-278 ◽  
Author(s):  
Konstantin Popov ◽  
S.M. Pesic ◽  
Predrag Zivkovic
Keyword(s):  
Process Parameters ◽  
Current Distribution ◽  
Current Density ◽  
Electrochemical Cell ◽  
Side Wall ◽  
Cell Geometry ◽  
Electrode Edge ◽  
Side Walls ◽  
In Cells

Anew method for the determination of the ability of an electrolyte to distribute uniformly current density in an electrochemical cell is proposed. It is based on the comparison of the current in cells in which the electrode edges touch the cell side walls with the current in cells with different electrode edge ? cell side wall distances. The effects of cell geometry process parameters and current density are discussed and illustrated using the results presented in the previous papers from this series.

scholarly journals A Novel H+ Conductance in Eosinophils

1999 ◽  
Vol 190 (2) ◽  
pp. 183-194 ◽  
Author(s):  
Botond Bánfi ◽  
Jacques Schrenzel ◽  
Oliver Nüsse ◽  
Daniel P. Lew ◽  
Erzsébet Ligeti ◽  
...  
Keyword(s):  
Nadph Oxidase ◽  
The Novel ◽  
Experimental Conditions ◽  
Intact Cells ◽  
Electrophysiological Studies ◽  
Dependent Signal ◽  
Low Threshold ◽  
Nadph Oxidase Activation ◽  
In Cells

Efficient mechanisms of H+ ion extrusion are crucial for normal NADPH oxidase function. However, whether the NADPH oxidase—in analogy with mitochondrial cytochromes—has an inherent H+ channel activity remains uncertain: electrophysiological studies did not find altered H+ currents in cells from patients with chronic granulomatous disease (CGD), challenging earlier reports in intact cells. In this study, we describe the presence of two different types of H+ currents in human eosinophils. The “classical” H+ current had properties similar to previously described H+ conductances and was present in CGD cells. In contrast, the “novel” type of H+ current had not been described previously and displayed unique properties: (a) it was absent in cells from gp91- or p47-deficient CGD patients; (b) it was only observed under experimental conditions that allowed NADPH oxidase activation; (c) because of its low threshold of voltage activation, it allowed proton influx and cytosolic acidification; (d) it activated faster and deactivated with slower and distinct kinetics than the classical H+ currents; and (e) it was ∼20-fold more sensitive to Zn2+ and was blocked by the histidine-reactive agent, diethylpyrocarbonate (DEPC). In summary, our results demonstrate that the NADPH oxidase or a closely associated protein provides a novel type of H+ conductance during phagocyte activation. The unique properties of this conductance suggest that its physiological function is not restricted to H+ extrusion and repolarization, but might include depolarization, pH-dependent signal termination, and determination of the phagosomal pH set point.

Determination of Acid Phosphatase Activity in Cells of Prostatic Tumours

Nature ◽  
1960 ◽  
Vol 188 (4751) ◽  
pp. 663-664 ◽  
Author(s):  
P. L. ESPOSTI ◽  
B. ESTBORN ◽  
J. ZAJICEK
Keyword(s):  
Acid Phosphatase ◽  
Phosphatase Activity ◽  
Acid Phosphatase Activity ◽  
In Cells
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