Daniel:Notebook/HiResChrPaint/2013-10-22: Difference between revisions
Jump to navigation
Jump to search
>Djacobse (→qPCR) |
>Djacobse (→qPCR) |
||
Line 63: | Line 63: | ||
5. [[Daniel:Protocols/Qiaquick_Column|Column Purification]], elute with 40 uL EB | 5. [[Daniel:Protocols/Qiaquick_Column|Column Purification]], elute with 40 uL EB | ||
6. Measure concentrations in nanodrop | 6. Measure concentrations in nanodrop | ||
===aqPCR Results=== | |||
[[Image:2013-10-22-BSPPControl.png|600px]] |
Revision as of 00:05, 23 October 2013
BSPP Control
- For first production of BSPP control, see 09/03/2013
Since I'm out of control group, I'm going to make some more.
qPCR
1. Reaction Table
10 nM OligoPool | 2X Kapa SYBR qPCR MM | 100 uM AP1V61U-Amino | 100 uM AP2V6 | H20 | Total Volume | |
per rxn | 0.4 | 50 | 0.4 | 0.4 | 48.8 | 100 |
BSPP 1 (12.5x) | 5 | 625 | 5 | 5 | 610 | 1250 |
BSPP 2 (12.5x) | 5 | 625 | 5 | 5 | 610 | 1250 |
2. Aliquot 100 uL into each of 12 qPCR tubes 3. PCR protocol: i. PCR 3 min 95C ii. 95C 3 sec iii. 55C 30 sec iv. 72C 20 sec v. plate read vi. goto ii x17 vii. 72C 2 min viii. 16C hold 4. Pooled 3 samples together each (300 uL each, 4 pools per set, 8 total) 5. Column Purification, elute with 40 uL EB 6. Measure concentrations in nanodrop