Web14 jan. 2014 · IDT offers a Resuspension Calculator as part of our SciTools™ suite, which is useful for calculating the volume of buffer to add to a dried down oligo to obtain … Web8 aug. 2024 · It is recommended to briefly centrifuge the tubes of dried oligo prior to opening them. This will ensure that the oligo pellet is at the bottom of the tube and will not be lost when the cap is...
Storage and handling of primers, custom oligos and BHQ Probes
Web31 mrt. 2024 · We recommend resuspending oligos in a TE buffer solution, such as IDTE, to maintain a constant pH that supports oligo stability (IDTE is available from IDT at pH 7.5 and pH 8.0). Alternatively, resuspend oligos in nuclease-free, sterile water, pH 7.0 … MGB Eclipse probes and companion primers are manufactured under ISO … Figure 3. IDT gBlocks and gBlocks HiFi Gene Fragments produce a higher … The IDT xGen hybridization capture products includes a variety of … Follow these steps to resuspend Alt-R™ HDR Donor Blocks: Before opening the … IDT recommends you aim for primers between 18–30 bases; however the … Unless otherwise agreed to in writing, IDT does not intend for these products to be … IDT offers a wide array of primer and probe sets, as well as plasmid controls, for the … Product details. Affinity Plus DNA & RNA Oligonucleotides are locked nucleic … WebThe present invention concerns a system for phenotypical profiling of at least one object and deterministic nanoliter-droplet encapsulation, comprising sample supplying means, buffer supplying means; a microfluidic chip comprising an encapsulation area or structure in which the object is encapsulated with a quantity of the reaction buffer by the droplet; detection … shanon woodruff
Resuspending freeze-dried oligonucleotides - Clark University
WebUse the free IDT OligoAnalyzer™ software to help ensure that primer and probe sets lack hairpins and homo- and heterodimer interactions. From there, you can link directly to the NCBI BLAST™ tool to further analyze … WebFor example, use a 10 µM stock and prepare a 1:5 dilution. We use up to 3 picomoles of primer in 12 µl sequencing reactions. Primer sequences. The conserved rDNA primers … Webis low you can resuspend the oligo in twice the volume to create a more dilute 50 μM stock solution. Vortex thoroughly and repeatedly for a minimum of 30 seconds, until no further particulates are observed in the bottom of the tube. 4. Next, dilute a portion of the stock solution to an appropriate working concentration. Once diluted, aliquot shanon whitelock