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A A schematic description of the homogenization of fiber network formed during a non-isothermai crystaiiization process by kinetically controiiing the nucieation of fibers, by kinetically inhibiting the nucieation of fibers to suppress the fiber formation during the early stage of a cooling process T j, a

A A schematic diagram depicting the angular-dependent nature of Metal-Enhanced Fluorescence. The real-color photographs show the fluorescence emission taken at an angle of 225 degrees .

A A schematic diagram depicting the processes in close proximity to metals involved in Metal-Enhanced Fluorescence

A A schematic diagram of a silica particle trapped in the center of a TFCD and a confocal fluorescent microscopy image of fluorescent silica particles trapped in a TFCD array

A A schematic diagram of a triple quadrupole during a selected reaction monitoring present in nearly all natural chemical species and are not drawn to scale.

A A schematic diagram of absorption spectra of the same substance at two different concentrations

A A schematic diagram of equine Cyt c from the front of the heme crevice. The approximate positions of the 8-carbons of the lysine residues are indicated by closed and dashed circles for residues located toward the front and back of the molecule, respectively. Differential chemical modification indicates that some residues are protected by both flavocytochrome c-552 and mitochondrial redox partners . Data for mitochondrial redox partners are from Ref. 98. In the case of the mitochondrial redox partners, R values for lysines 55, 72 and 99 are average values for lysines 53-t-55, 72 73 and 99 100. The R values represent, after a series of corrections, the ratio of acetylation of a specific lysine residue in free Cyt c to the acetylation of the same residue in the Cyt c

A A schematic diagram of the experimental set-up .

A A schematic diagram of the finai structures in the sampies prepared at different poiymer concentrations .

A A schematic drawing of a system of three spins labeled 1,2, and 3. When spin 1 and spin 2 have correlation while spin 3 is isolated, the cross-peak between 1 and 2 appears, as depicted in .

A A schematic drawing of an array of one-dimensional spectra of a homo-nuclear three-spin system with incremented evolution time q. We suppose that the magnetizations of the spins labeled with i, j, and k change with time as depicted in . Since the way that the magnetizations of and k change with is somewhat correlated, a covariance cross-peak appears between and k, as drawn in Q, whereas the time dependence of the j magnetization is quite different from others, resulting in no appreciable covariance cross-peaks.

A A schematic illustration of a microfiuidic cell culture chip with a Drosophila melanogaster embryo exposed to cold and warm medium in a gradient forming intersection of two merging fluidic paths A finite element simulation to visualize generation of a stable gradient in perfusion systems.

A A schematic illustration of the GABAb.

A A schematic image of an atomic force microscope. A laser beam is reflected at the back of the triangular cantilever. A picture of an atomic force microscope which is combined with an optical microscope. The white box indicated by an arrow consists of the AFM unit including the piezo. A step motor causes the box to move up and down.

A A schematic of globular actin monomer forming a protein filament, called F-actin. This filament is one of the important components of muscle cells, as well as the cytoskeleton of other cells. Oriented actin filaments inside a fibroblast cell, called stress fibers, seen through a fluorescence microscope. Image obtained from Nguyen et al. and reprinted with permission.

A A schematic of the group I ribozyme open complex, with the location of the spin label marked by the dot. Variations in PI motions upon mutating the Jl 2 junction from AAA to UUU . Adapted from ref. 69 with permission.

A A schematic of the microfabrication process of a conducting IPN microactuator

A A schematic representation of a cross section of a two-dimensional electric dipole array. except that the dipole array is at the hydrocarbon aqueous interface in this case.

A A schematic representation of a neurotransmitter filled vesicle fusing with the

A A schematic representation of NH4 movement through the quadruplex

A A schematic representation of the folding of the chromatin fiber caused by continuous unwinding of the internucleosomal linker domains. Proc. Natl. Acad. Sci. USA 95, 14173-14178, with permission from Portland Press Biochemical Society, Springer Verlag, and The National Academy of Sciences.

A A schematic representation of the rod photoreceptor cell and the intracellular disk membrane organelles and its counterion, respectively. Diamond symbols mark residues that are highly conserved throughout the rhodopsin subfamily of GPCRs. Sequences at the cytoplasmic surface directly involved in transducin interaction are shaded. These same sequences are also implicated in binding of the regulatory proteins arrestin and rhodopsin kinase. Zigzag lines at 322C and 323C represent palmitoyl residues, while phosphorylation sites in the C-terminal tail are marked by filled square symbols.

A A schematic representation of the three-dimensional structure of the PLC- A model of the conformational change of the PLC-51 PH domain-induced at the membrane surface.

A A schematic structure of the orthoclase lattice. The a and p planes are indicated on the left. ,

A A schematic view of the proximity of a ceU to the surface of a planar electrode and the reaction of dopamine oxidation.

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