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Phylogenetic placement of the enigmatic longhorned beetle Vesperoctenus flohri Bates (Vesperidae) and a first description of its female internal structures
…68–89). We describe and discuss the phylogenetic significance of the internal structures of a recently collected V. flohri female from the Sierra de la Laguna mountain range in Mexico, the…
Morphological cell profiling of SARS-CoV-2 infection identifies drug repurposing candidates for COVID-19
…can significantly accelerate translation. We developed a quantitative high-throughput screen to identify efficacious agents against SARS-CoV-2. From a library of 1,425 US Food and Drug Administration (FDA)-approved compounds and clinical…
What are options to analyze my samples after running myTXTL reactions when using the system for protein production?
Apart from standard biochemical methods like Coomassie-stained SDS-PAGE and western blot analysis, the great advantage of cell-free protein production is the open-system environment which allows the direct quantification and/or analysis…
There is a fully sequenced genome available for my organism – can you use this to make WGE baits?
The myBaits WGE product line ONLY offers bait production directly from high quality genomic DNA precursor material. This gDNA must be made physically available to us in order to manufacture…
What sample evaluation/QC measures are taken for my samples sent for NGS laboratory services?
…enter our QC queue. For Standard and Long Insert quality DNA samples, we will quantify the total gDNA with a spectrofluorometric assay, purify up to 80% of the material, and…
A HYBRID CAPTURE BAIT SET FOR BEGONIA
…in shade adaptation and development and genetically linked to key traits. We demonstrate successful recovery of sequence data from species across Begonia and from fresh, silica-dried and older herbarium material….
What additives are tolerated by the myTXTL system?
It may be necessary at times to add components to the myTXTL system from sources that contain material of unknown effect in the myTXTL system, the following is a guide…
Protein engineering
…analysis in hours not days. Supporting linear DNA templates to reduce time and costs compared to cloning DNA into plasmids (plasmid DNA is also supported). Eliminating the need for additional…
Can I input less than the recommended library mass per myBaits reaction?
…input of sufficiently complex libraries. For best results, it is recommended that only amplified (non-PCR-free) NGS libraries are used for target capture. This provides multiple copies of each starting template…
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