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Polyamides (nylons) are synthetic analogs of proteins having the amide groups separated by hydrocarbon chains, (CH2)n, and can be made with an excess of either terminal amino (−NH2) or terminal carboxyl groups (−COOH).
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Thus, accurate delineation of the nature of the imbalance, either terminal or interstitial, is crucial for diagnosis and prognosis.
Mapping some morphological traits commonly used in the classification of Algansea onto the molecular phylogenies clearly shows that the orientation of the mouth, either terminal or upturned, represents a homoplasious character.
The text is presented in three general sections according to the dimensionality of the coordination polymer, and then is subdivided in sections that take into account the structural role of the nucleobase as ligand (either terminal or bridging), and the nature of the nucleobase (pyrimidine vs purine).
Deletion mutants of either the N-terminal or C-terminal domain were constructed by ligating either the EcoRI/BamHI or EcoRI fragment of pIRES1neo/Scr3 into the EcoRI/BamHI site of pEGFP-C2 or into the EcoRI site of pEGFP-C1, and the resultant plasmids are designated pGFP-Scr3ΔN and pGFP-Scr3ΔC, respectively.
A similar effect was proven in other DEAD-box helicase related genes, such as the UAP56 [ 36] and DP103 [ 37], where the deletion of either the N-terminal or C-terminal flanking sequences outside the domain core regions impacts their helicase and ATPase activity, signifying the regulatory roles of the flanking regions.
HEK 293T cells were transfected to express c-myc tagged recombinant forms of either the NH2-terminal half (A2ML1 1–889) or the COOH-terminal half of A2ML1 (A2ML1 990–1454).
The GFP cassette was amplified from GFP-pBSpuro cassette [63] with 50 nucleotides of EBV genome (151,959-152,008 and 152,008-152,058) at either terminal of the cassette (Figure 1A); the amplified cassette was then transfected in EL350 with MD1BAC for homologous recombination and the clones were screened on amp-kan plate (kanamycin was already inserted into BAC EBV in MD1BAC [29]).
Previous studies have shown that deletion of either the N-terminal 30 aa of LANA, which eliminates the Region I cluster of basic amino acids and disrupts the classical bipartite kr-NLS, or deletion of the N-terminal 50 aa of LANA, which completely eliminates the kr-NLS, prevents nuclear localization of full-length LANA [48].
Nevertheless we investigated the NLS in more detail and showed that mutations destroying the functionality of the NLS did not completely abolish the nuclear translocation of either the N-terminal or the full length GFP fusion proteins in either aPKC.
Press the red probe against either terminal screw of the heating element.
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