Sentence examples for verified full length from inspiring English sources

We created stable cell lines expressing either wild type human clathrin cDNA or human temperature-sensitive clathrin (TS-clathrin), by using human clathrin heavy chain cDNA under a constitutive CMV (cytomegalovirus) promoter (verified full length cDNA clone IRATp970E0575D from RZPD  =  Deutsches Resourcenzentrum fuer Genomforschung GmbH; accession number: Uniprot Q00610).

We BLASTed our conserved blocks against a large dataset of experimentally verified full length cDNA sequences from P. falciparum and P. yoelii and manually inspected the results.

For that purpose, a standard curve was established using serial dilutions of a recombinant plasmid containing verified full-length PAR1 clone.

There is currently a non-redundant set of over 13,000 sequence verified, full-length ORF human clones in the MGC collection.

To verify full length GFP expression, all plates were harvested at 72 hours, after which time the cells were lysed, GFP protein was purified and examined by western blot analysis using anti-His antibodies (figure 3B).

In addition, most copies of Novel_NA_RP (604/881) were the verified full-length elements, suggesting that this family might experience a burst of transposition in R. prolixus.

From 1961 sequence-verified full-length clones representing 96% of protein coding F. tularensis ORFs, we successfully expressed and purified 72% of the proteins.

To establish an A.2 cell line that constitutively expressed UBP43, the UBP43 open reading frame was generated by PCR from a sequence-verified full-length cDNA purchased from Open Biosystems.

Sequence-verified full-length cDNA clones with high accuracy that harbor protein coding sequences are critical for advances in structural, functional and comparative genomic studies.

A total of 768 sequence-verified full-length human genes in pANT7_cGST or pLDNT7_nFLAG were obtained from the Center for Personalized Diagnostics at the Arizona State University and are publicly available [ 20].

To circumvent the aforementioned limitations with existing yeast arrays, we combined the sequence-verified Full-Length EXpression-ready (FLEX) plasmid library of galactose-inducible untagged ORFs (Hu et al. 2007) with a set of Barcoder yeast strains, which are compatible with parallel competitive growth analysis.