The energy storage can be identified from non-potentiality of the source region such as magnetic shear or accumulated helicity (Tsurutani et al. 2009a; Kazachenko et al. 2012).
The cutting force and process damping coefficients at different parts of the drill lip are identified empirically; the cutting force coefficients are identified from non-symmetric drilling tests, and the process damping coefficients are identified from chatter-free orthogonal turning tests.
Interestingly, two WRKY homologues were identified from non-plant eukaryotic species, and both have two WRKY domains [see Additional files 1 and 2].
This is because no similar protein motif was identified from non-redundant protein database searches, and it is not easy to speculate their protein function even if they were translated.
Recently, several WRKY genes were identified from non-plant eukaryotes, including Dictyostelium discoideum, a slime mold closely related to the animal and fungi lineages, and the green alga Chlamydomonas reinhardtii, an early branch of plants.
Recently, several cathelicidins have been identified from some non-mammalian vertebrates including hagfish [27], rainbow trout [28], [29], atlantic salmon [29], and chicken [30], [31].
After analyzing the proteomics data according to the stringent criteria, a total of 3,010 proteins and 3,224 proteins were identified from the non-diabetic and diabetic serum, respectively.
However, these proteins were identified from the non-infective stage, and their presence in the infective stage of the parasite needs to be confirmed prior to further studies on their use in vaccines.
The results of volatile analyses demonstrated that more than 90 constitutive and inducible compounds from volatile blends have been identified from host and non-host plants (see Table S1, 2, 3, 4).
Closely related homologs were identified from the NCBI non-redundant database using BLASTP searches.
Hundreds of proteins with various defined key cellular functions were identified from TNBC and non-TNBC tumors.
