For vehicles that disappear at image borders or below bridges during an exposure of the sequence (but have been detected or tracked in the image before) the tracking algorithm does not dump a match.
Vehicle tracking was tested on the same data takes obtained at a flight height of 1,000 m (15 cm GSD), 1,500 m (21 cm GSD), and at a flight height of 2,000 m (30 cm GSD). Figure 6 shows a typical result on tracking vehicles from the first image of an image sequence into the second exposure of the sequence.
The micrograph depicted in Figure 2b is a plan view of the nanostructured surface after exposure to the sequence of CF4 and O2 plasma steps and the final HCl/H2O surface cleaning described above.
LLP2-specific MAbs did not bind when effector and target cells were incubated at 37°C, indicating a highly transient exposure of the LLP2 sequence [23], consistent with prior reports of LLP2 membrane association post-fusion [24].
The highest binding affinities are observed with full exposure of the aptamer sequence in the loop, while duplex formation reduces binding affinity most likely due to the thermodynamics of DNA base pairing.
Although the RGD sequences within collagen and laminin are not normally exposed, denaturation or cleavage of these proteins may result in exposure of the RGD sequence and subsequent integrin binding.
We deduced that it is relatively easy for the primer or probe and the DNA polymerase to bind to the target region of the linear plasmid compared with that of the undigested supercoil plasmid, because of the exposure of the target sequence of the digested plasmid.
The activity of XIAP is antagonised by SMAC/DIABLO (second mitochondria-derived activator of caspase/direct inhibitor of apoptosis-binding protein with low pI), that, on release from mitochondria in response to apoptotic stimuli (Du et al, 2000), undergoes maturation and cleavage of its N-terminal region, allowing the exposure of the AVPI sequence.
Most sRNAs are 80 200 nt long and directly bind to their target mRNAs in the 5′-UTR or in the open reading frame to execute their regulation activity by changing the exposure of the SD sequence of mRNAs to ribosomes or altering the stability of mRNAs.
Karstification and in situ solution brecciation developed extensively during exposure of the upper sequences (Fig. 7g), while the pore types are mainly inter-granular dissolved pores, moldic pores, and vugs (Fig. 7b, c).
Surface exposure of the interactive sequences is expected for the functional effects of αB crystallin on microtubule assembly which can only occur on the surface of dissociated subunits of αB crystallin or tubulin.
