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Briefly, double-stranded cDNA's were synthesized using oligo dT) beads and cDNA's were digested with NlaIII or DpnII restriction enzymes and ligated to defined gene expression adapter (GEX NlaIII Adapter 1, containing another restriction enzyme MmeI).
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Double-stranded cDNAs were cleaved at DpnII restriction sites, and gene expression adapters 1 and 2 were ligated to the DpnII cleavage and the MmeI cleavage site, respectively, using T4 DNA ligase.
Gene expression (GEX) adapters 1 were ligated to the DpnII cleavage sites using T4 DNA ligase (Invitrogen).
NucARRB1 and wtARRB1 cellscells proliferated faster than control cells, whereas ARRB1 KD decreased cell proliferation (Fig 2B D), implying a dependency on adapter expression.
Additionally we observed expression of the adapter protein shc, phospholipase-Cγ (PLCγ) and p44 MAP kinase, which are involved in VEGFR-2 and -3 signal-transduction (review: 2).
Recently it was shown that cases of human melanomas have a severely diminished expression of the adapter protein Apaf-1 and are concomitantly resistant to apoptosis (Soengas et al, 2001).
Gene expression analysis of these adapter proteins and related genes showed some differences between hESC and the adult endothelial cells.
On this basis, we and others advanced the notion of Ad targeting based on expression of secreted paracrine adapter molecules encoded in the vector genome as a means of retaining targeting capacity of conditionally replicating Ad vectors (CRAds) [29] [32].
Immunohistochemical analyses revealed that expression of p62, an adapter protein between ubiquitin and autophagosome, was elicited on autophagosomal membranes in the AVP neurons, suggesting selective autophagy induction at this time point.
Eike R. Hrincius (University of Münster) presented data demonstrating that the non-structural protein 1 (NS1) of Influenza A virus binds to the cellular adaptor proteins Crk and CrkL, tereby determining the sensitivity of influenza viruses to the expression of the two adapter proteins.
The compiled collection of expression tags with removed adapters was initially aligned against the reduced-complexity set of RefSeq entries and the targets reference sequences were filtered as in the microarray probe mapping to exclude any targets corresponding to different gene symbols or with no associated gene symbol.
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