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solute concentration on the membrane surface (g L−1).
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Second, immunoelectron microscopy (Griffiths and Hoppeler 1986) was used to label the same glycoprotein in ultrathin sections of infected cells and obtain an LD over membranes, expressed as the number of gold particles per μm of membrane surface (N g / S c ).
Scanning electron microscopic picture of human amniotic membrane: e unprocessed membrane with amniotic epithelial cells, f basement surface of unprocessed membrane, g decellularised membrane with the impressions of cellular basement and h basement surface of processed membrane.
This phenomenon was attributed to the further accumulation of SMA-g-MPEG additives on membrane surface in aqueous conditions.
Microstructural parameters including crystal size (d) and shape (M), apparent surface porosity (Ra) and average grain boundary (G) are used to quantify the membrane surface morphology.
We observed the presence of two morphologically distinguishable cell populations in the 1 g cultured samples: one has smooth membrane surface and the other one is characterized by the presence of membrane expansions morphologically similar to microvilli.
Cells expressing the truncated G-CSFR form exhibit increased receptor expression at the membrane surface, which correlates with sustained intracellular activation and enhanced growth and survival responses to G-CSF [10], [29] [31].
A third scenario that is not considered is similar to the first case where the G-field is parallel to the membrane surface.
Sulfonic groups could be further introduced into the poly styrene) grafts of ETFE-g-PBrTFF-g-PS films with homogeneous distribution in a perpendicular direction to the membrane surface.
(G) Immunoblots and densitometric analysis of Kv2.1 expression on membrane surface, with either flotillin-1 knockdown or overexpression of flotillin-1 in the presence or absence of MG132.
We further assume that the membrane surface concentration of free glycan receptor can be approximated as a constant, [ G ′], at the short time limit.
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