WebEmploy calculators to analyze oligos including concentrations, sequence-specific properties, melting temperatures, and other parameters. Design basic or highly modified … WebHigher purity options will also work. PCR using oligos with critical 5´ sequences (e.g., restriction endonuclease sites, RNA polymerase promoters) Cartridge, HPLC, and PAGE-purified oligos are best for the greatest efficiency. Since oligos are synthesized 3´ to 5´, incomplete oligos (n-x oligos) will be missing the 5´ sequence.
Fisher
WebThe sodium equivalent is calculated as follows: [Na +] = Monovalent ion concentration + 4 × (Free Mg 2+) 1/2 (all in molarity) The default value = 382.84 mM. Temperature for Free Energy Calculation. This is used to calculate the Gibbs free energy (ΔG) in the formula: ΔG = ΔH - T ΔS. The default value = 25.0 °C (298K). WebDec 30, 2015 · It is valid for oligos longer than 50 nucleotides from pH 5 to 9. Symbols and salt adjustment term as above, with the term (41 * (yG + zC-16.4)/(wA + xT + yG + zC)) adjusting for G/C content and the term (500/(wA + xT + yG + zC)) adjusting for the length of the sequence, and F is the percent concentration of formamide. small wooden outdoor table
OligoCalc: Oligonucleotide Properties Calculator
WebIn addition to our custom synthesis options for oligos, primers, probes, and genes, we offer random primers, Oligo (dT) primers, 5’ labeled primers, gene specific primers for sequencing, forward and reverse sequencing primers and kits. Order now. Value Oligo formats. Pay per oligo, 25 and 50 nmol synthesis scales, up to 40 bases, no ... WebJul 28, 2024 · Welcome to a quick tutorial on how to use the Thermo Fisher Scientific Oligos Ordering Portal. In this video we'll discuss how to navigate and use the Oligos Ordering Portal, including how to order standard, plate, and custom oligos, and alternatively how to bulk order multiple oligos at one time. WebFeb 10, 2024 · The destination vector was digested overnight with AAR1 (Thermo Fisher). Oligos were diluted to 100 μM, and 50 μL forward and reverse oligos were annealed with 900 μL buffer (10 mM Tris, pH 7.5) and placed at 98 °C for 3 min, then room temperature for 10 min. Oligos (8μL) were then ligated into the digested vector (1 μL) using T4 ligase ... hikvision tracking camera