Daniel:Notebook/HiResChrPaint/2013-4-15: Difference between revisions
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===Dye Coupling Reaction=== | ===Dye Coupling Reaction=== | ||
Thaw out oligos, sodium bicarbonate solution, DMSO | 1. Thaw out oligos, sodium bicarbonate solution, DMSO | ||
Use thermo device on Noi's desk to heat DMSO, sodium bicarb to 42 C | Use thermo device on Noi's desk to heat DMSO, sodium bicarb to 42 C | ||
Add 2.5 uL DNA, 1.5 uL sodium bicarbonate to 0.2 mL eppendorf | 2. Add 2.5 uL DNA, 1.5 uL sodium bicarbonate to 0.2 mL eppendorf | ||
Thaw out dyes (they are in big -20C) and resuspend in 2.2 uL DMSO | 3. Thaw out dyes (they are in big -20C) and resuspend in 2.2 uL DMSO | ||
Add 1 uL of appropriate dye to oligo set (see below) | Use dyes immediately, they do not store | ||
4. Add 1 uL of appropriate dye to oligo set (see below) | |||
[[Daniel:Notebook/HiResChrPaint|Back to Calendar]] | [[Daniel:Notebook/HiResChrPaint|Back to Calendar]] |
Revision as of 18:15, 15 April 2013
Dye Coupling Test and Gel Quantification
Purpose: Test dye coupling reaction, specifically the purification step, to ensure proper dye-coupled DNA is being captured. Two samples chosen from Gel Quantification (4/10/13). Oligos coupled to appropriate dye.
Dye Coupling Reaction
1. Thaw out oligos, sodium bicarbonate solution, DMSO Use thermo device on Noi's desk to heat DMSO, sodium bicarb to 42 C 2. Add 2.5 uL DNA, 1.5 uL sodium bicarbonate to 0.2 mL eppendorf 3. Thaw out dyes (they are in big -20C) and resuspend in 2.2 uL DMSO Use dyes immediately, they do not store 4. Add 1 uL of appropriate dye to oligo set (see below)