Daniel:Notebook/HiResChrPaint/2013-7-11: Difference between revisions
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4. Incubate for 15 minutes (AmpR9) or 20 minutes (AmpR10) at 80C, snap cool on ice | 4. Incubate for 15 minutes (AmpR9) or 20 minutes (AmpR10) at 80C, snap cool on ice | ||
5. Purify using [[Daniel:Protocols/CentriSep|Centri-Sep Column]] | 5. Purify using [[Daniel:Protocols/CentriSep|Centri-Sep Column]] | ||
===Results=== | |||
{| class="wikitable" <hiddentext>generated with [[:de:Wikipedia:Helferlein/VBA-Macro for EXCEL tableconversion]] V1.8</hiddentext> | |||
|- style="font-size:12pt" align="center" | |||
| align="center" width="65" height="30" | | |||
|style="font-weight:bold" width="65" | ng/uL DNA | |||
|style="font-weight:bold" width="65" | pmol/uL dye | |||
|style="font-weight:bold" width="65" | ug DNA in 20 uL | |||
|style="font-weight:bold" width="71" | pmol/uL DNA | |||
|style="font-weight:bold" width="71" | dye/probe | |||
|style="font-weight:bold" width="71" | dye/100 bp | |||
|style="font-weight:bold" width="65" | Base:Dye Ratio (:1) | |||
|- style="font-size:12pt" align="center" | |||
|style="font-weight:bold" height="15" | AmpR9 | |||
| align="center" | 64.6 | |||
| align="center" | 0.6 | |||
| align="center" | 1.3 | |||
| align="center" | 3.9 | |||
| align="center" | 0.2 | |||
| align="center" | 0.3 | |||
| align="center" | 326 | |||
|- style="font-size:12pt" align="center" | |||
|style="font-weight:bold" height="15" | AmpR10 | |||
| align="center" | 71.1 | |||
| align="center" | 0.4 | |||
| align="center" | 1.4 | |||
| align="center" | 4.3 | |||
| align="center" | 0.1 | |||
| align="center" | 0.2 | |||
| align="center" | 539 | |||
|} | |||
It would seem that I can always tell beforehand whether a yield will be good or bad, by the color of | |||
the solution post incubation. If the solution has a faint green color it will be a good yield. If | |||
the solution remains clear it will be a bad yield. Therefore I'm going to ignore columns for future | |||
trials (yes, it looks like I need more troubleshooting). That will save on time and $$, and hopefully | |||
I'll get to the bottom of this before long. |
Revision as of 19:46, 11 July 2013
S2 Probe Prep (Started 5/29/2013)
ULYSIS Dye Coupling (Test 6)
Should be the last test. I'm going to test at 15 minutes and 20 minutes incubation time, 1 uL each. If the results go well this morning I will be labeling the V6S2 set this afternoon.
- Following ULYSIS protocol
1. Add 1 uL DNA in 19 uL labeling buffer (Component C) 2. Denature DNA for 5 minutes at 95C; snap cool on ice 3. Add 1 uL dye to sample; add 4 uL labeling buffer 4. Incubate for 15 minutes (AmpR9) or 20 minutes (AmpR10) at 80C, snap cool on ice 5. Purify using Centri-Sep Column
Results
ng/uL DNA | pmol/uL dye | ug DNA in 20 uL | pmol/uL DNA | dye/probe | dye/100 bp | Base:Dye Ratio (:1) | |
AmpR9 | 64.6 | 0.6 | 1.3 | 3.9 | 0.2 | 0.3 | 326 |
AmpR10 | 71.1 | 0.4 | 1.4 | 4.3 | 0.1 | 0.2 | 539 |
It would seem that I can always tell beforehand whether a yield will be good or bad, by the color of the solution post incubation. If the solution has a faint green color it will be a good yield. If the solution remains clear it will be a bad yield. Therefore I'm going to ignore columns for future trials (yes, it looks like I need more troubleshooting). That will save on time and $$, and hopefully I'll get to the bottom of this before long.