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Collagen alpha-1(VIII) chain is a protein that in humans is encoded by the COL8A1 gene. [5] [6]This gene encodes one of the two alpha chains of type VIII collagen.The gene product is a short chain collagen and a major component of the basement membrane of the corneal endothelium.
A pronounced double minimum at 208 and 222 nm indicate α-helical structure, whereas a single minimum at 204 nm or 217 nm reflects random-coil or β-sheet structure, respectively. A less common method is infrared spectroscopy, which detects differences in the bond oscillations of amide groups due to hydrogen-bonding.
This means that all redundant genes should theoretically become a pseudogene and eventually be lost. Scientists have devised two hypotheses as to why redundant genes can remain in the genome: the backup hypothesis and the piggyback hypothesis. [16] The backup hypothesis proposes that redundant genes remain in the genome as a sort of "back-up plan".
The beta sheet (β-sheet, also β-pleated sheet) is a common motif of the regular protein secondary structure. Beta sheets consist of beta strands ( β-strands ) connected laterally by at least two or three backbone hydrogen bonds , forming a generally twisted, pleated sheet.
Pigment color differs from structural color in that it is the same for all viewing angles, whereas structural color is the result of selective reflection or iridescence, usually because of multilayer structures. For example, butterfly wings typically contain structural color, although many butterflies have cells that contain pigment as well. [3]
The brilliant iridescent colors of the peacock's tail feathers are created by structural coloration, as first noted by Isaac Newton and Robert Hooke.. Structural coloration in animals, and a few plants, is the production of colour by microscopically structured surfaces fine enough to interfere with visible light instead of pigments, although some structural coloration occurs in combination ...
Safranin is used as a counterstain in some staining protocols, colouring cell nuclei red. This is the classic counterstain in both Gram stains and endospore staining. It can also be used for the detection of cartilage, [2] mucin and mast cell granules. Safranin typically has the chemical structure shown at right (sometimes described as dimethyl ...
This was termed a chromaticity cell. A third cell – also a chromaticity cell – responded with hyperpolarization at fairly short wavelengths, peaking about 490 nm, and with depolarization at wavelengths longer than about 610 nm. Svaetichin and MacNichol called the chromaticity cells yellow–blue and red–green opponent color cells.