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the g protein is capable of many interactions with the other membrane proteins. in order to characterize these interactions and to follow their time course, g-protein-deficient cells have been subjected to a variety of ways to trap the g protein-membrane protein interactions (sistow & shetfar 1969, sistow 1969). gtp is hydrolyzed at a high rate with a half-time of about 1 min. in this state the g protein is tightly bound to the membrane. the g protein can then be extracted by guanine nucleotide exchange factors, and also by other membrane permeant substances such as detergents. a g-protein that has been extracted from this way is no longer capable of interacting with the other membrane proteins that it has bound to in the membrane. when the extract is separated from the membrane by gel electrophoresis, the g-protein is found to move with the same mobility as the membrane proteins. this is usually taken to signify that the g protein is stably bound to the membrane, and that it has not been extracted.
in the context of genetic recombination, dna is considered to be linear and to move in the same direction as the replicating dna molecule. we show that dnas are in fact circular and move in the opposite direction to the replicating molecule.
to verify the speed of the download service, we connected to either a local jio sim or an iphone xs from a 3g mobile network in the eight telecom circles mentioned above. for each circle, we checked the iphone to see if an internet connection was detected and pulled off the download speed by pulling the low-level data from the modem in the iphone.
progressive increases in excitability after hyperpolarizing prepulses have been observed in both squid axon and photoreceptor cells (prato 1966). these changes are due to a time-dependent generation of an anomalous hyperpolarizing current carried by h+ ions (hutcheon et al. 1969, ting & mela 1968, mitchell et al. 1968, jakobson & johnson 1969). in squid axons, this voltage-dependent current(iv) is generated by modulation of a h+ current, (iv) which is normally repressed by membrane hyperpolarization (prato 1966).
many birds and insects are capable of the rapid discrimination of a large number of conspecific individuals using visual cues at a distance. theoretically, given the high variability of coloration of many insects and birds, thousands of potential discriminands can be visually matched in a two-dimensional space. the capacity of an individual animal to perform such a feat of discrimination in a single sweep of the retina is still unknown. however, birds could in theory build up a mental image, possibly using a template matching or pattern recognition mechanism. some highly specialized birds, such as the zebra finch, are extremely specialized for the identification of particular conspecifics based on particular song patterns, and are capable of recognizing up to 1000 song sequences. this ability requires extensive training with only one particular song type.
the lens can experience changes as a function of aging; in some species, crystallins are modified due to the deposition of amorphous or crystalline substances on the lens surface (ando & tinsley 1966). as a result, lens transparency and refractive power are diminished, and the lens can become opacified and myopic (prato & goldberg 1969). some protozoans have a crystalline lens. but it does not have the ability to change refraction at the eye; it is simply a transparent lens, like the more commonly encountered animal lens.
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