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https://www.atum.bio/pipeline/dna
ATUM is building on DNA2.0's reputation for rapid, reliable and accurate DNA synthesis. Using our proprietary GeneGPS® and VectorGPS® platforms we design constructs optimized to express in your system, whether that's a single gene in E. coli, a metabolic pathway in yeast or …
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We generally reply within a few hours. [email protected]. Atum in the World. Events. September 13-16 2021. 15th PEACe Protein Expression in Animal Cells Conference, Virtual. Virtual. ATUM's Oren Beske will present Monday September 13 at 12:15. September 15-16 2021. Cell & Gene Therapies 4th.
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https://www.atum.bio/assets/pdf/Pichia_Culture_and_Induction_Protocol6.pdf
5. Incubate transformations for 1-2 hours at 30°C and 200 rpm. 6. Spread 50, 100, and 200 µl to both YPDS + 250 ug/ml Zeocin and YPDS + 1000 ug/ml Zeocin plates. 7. Incubate the plates at 30°C for 2-3 days, until colonies are well formed. No colonies should grow on the negative control. 8.
https://www.atum.bio/resources/tools/gene-designer
ATUM’s intelligent, user friendly & customizable Genedesigner2.0 provides fast, easy algorithms for in silico cloning, codon optimization, back translation & primer design
https://guidetovaping.com/the-dna20/
Oct 10, 2013 · The DNA20 is a small board only measuring in at 0.65”x1.30”x0.35” off of it hangs a small ribbon cable with a 0.69” OLED screen to display the information. There are 3 on board buttons which can be used; A fire button, a wattage up and a wattage down button. In addition …
https://www.atum.bio/catalog/reagents/protein-paint-box
ProteinPaintbox® Synthetic non-Aequorea fluorescent and chromogenic proteins bring a world of color to your research.Overview. ATUM's synthetic fluorescent and chromogenic proteins (non-Aequorea) are an ideal source of protein coding sequences (genes) that can be easily excised using the flanking restriction sites and cloned into any other expression vector of choice.
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