Compared with the traditional radars, a 60-GHz millimeter-wave (mm-Wave) radar is promising to more adverse environmental conditions, e.g., fog, rain, and snow, which may recognize the target more accurately [1,2].
For example, the regulator B may recognize and target the one-dose gene A and suppress A's expression change before the fact.
Two possible explanations of these findings are that activators or repressors recruited by feedback-regulated genes could locally spread to neighboring genes, thus causing a general buffering effect for aneuploid regions, or currently unknown buffering mechanisms may recognize and target aneuploid regions of the genome.
For a given S-haplotype, two or more types of SLF proteins may recognize and target the degradation of a particular non-self S-RNase (Kubo et al. 2010), and thus loss of function in a single type of SLF gene may not affect the SI behaviour of pollen, because products of some other type(s) of SLF gene(s) may also recognize the same non-self S-RNase targeted by the defective SLF.
Based on their observations, Papo and Shai proposed that AMPs, which are positively charged molecules, may "recognize" negatively charged targets such as cancer cells and bacteria [49].
Data in the literature suggest several, not mutually exclusive, possibilities of how SET proteins may recognize their chromatin targets.
Bacterial sRNAs may recognize their cognate target mRNAs in different ways.
They may recognize CCTTC or similar target site with 1-bp difference.
These facts indicate that miRNAs associated with miRNPs may recognize uAUG sequences as target sites and prevent translation.
These distinct binding patterns implied that these antibodies may recognize different sites of the target molecule, which are unequally exposed in the different ELISA formats, and work is now in progress to characterize these clones further.
