Daniel:Notebook/HiResChrPaint/2013-7-22: Difference between revisions

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===Nanodrop Results===
===Nanodrop Results===
{| class="wikitable" <hiddentext>generated with [[:de:Wikipedia:Helferlein/VBA-Macro for EXCEL tableconversion]] V1.8</hiddentext>
|- style="font-size:12pt;font-weight:bold" align="center"
| width="65" height="15" | Sample
| width="65" | V4S4A
| width="65" | V4S4B
| width="65" | V4S4C
| width="65" | V4S4D
| width="65" | V6S4A
| width="65" | V6S4B
| width="65" | V6S4C
| width="65" | V6S4D
|- style="font-size:12pt" align="center"
|style="font-weight:bold" height="15" | ng/uL
| align="center" | 52.6
| align="center" | 44.5
| align="center" | 52.1
| align="center" | 47.4
| align="center" | 105.7
| align="center" | 111.3
| align="center" | 98.1
| align="center" | 103.3
|- style="font-size:12pt" align="center"
|style="font-weight:bold" height="15" | ug in 40 uL
| align="center" | 2.1
| align="center" | 1.8
| align="center" | 2.1
| align="center" | 1.9
| align="center" | 4.2
| align="center" | 4.5
| align="center" | 3.9
| align="center" | 4.1
|- style="font-size:12pt" align="center"
|style="font-weight:bold" height="15" | Total ug
| align="center" | &nbsp;
| align="center" | &nbsp;
| align="center" | &nbsp;
| align="center" | 5.8
| align="center" |
| align="center" |
| align="center" |
| align="center" | 12.5
|}
==DpnII Digestion==
1. Prepare Samples
2. Incubate samples at 37C for 16 hours; 20 minute heat shock at 65C; [[Daniel:Notebook/HiResChrPaint/2013-7-23|Continued]] 7/23/2013]]

Revision as of 00:37, 23 July 2013

S2 Probe Preparation

Back to Calendar

Despite mixed reviews from the S4 set, I'm going to go ahead and make the S2 set. Also, I talked with Alan and he and I are going to prep some cells tomorrow. I'll probably go ahead and attempt fish with the S3 set, since that one worked out great. If I have other probes available, I may use them as well, but Alan and I won't be preparing the cells until tomorrow afternoon, which gives me plenty of time to prep a new set.

PCR Amplification

1. Reaction Table
  20 nM OligoPool 2X Kapa SYBR qPCR MM 100 uM AP1V41U 100 uM AP2V4 100 uM AP1V61U 100 uM AP2V6 2 mM aa-dUTP H20 Total Volume
per rxn 0.2 50 0.4 0.4 0.4 0.4 2.5 45.7 100
V4S3 (12.5x) 2.5 625 5 5 0 0 31 581.5 1250
V6S3 (12.5x) 2.5 625 0 0 5 5 31 581.5 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. Ethanol Precipitation, added 900 uL 100% EtOH, 30 uL 3 M NaOAc, 1 uL glycoblue
6. Incubated 4 hours; resuspend in 50 uL nfH20
7. Column Purification, elute with 40 uL EB
8. Measure concentrations in nanodrop

qPCR Results

File:2013-7-22-S2.png

Nanodrop Results

Sample V4S4A V4S4B V4S4C V4S4D V6S4A V6S4B V6S4C V6S4D
ng/uL 52.6 44.5 52.1 47.4 105.7 111.3 98.1 103.3
ug in 40 uL 2.1 1.8 2.1 1.9 4.2 4.5 3.9 4.1
Total ug       5.8 12.5

DpnII Digestion

1. Prepare Samples


2. Incubate samples at 37C for 16 hours; 20 minute heat shock at 65C; Continued 7/23/2013]]