Team:BYU Provo/Notebook/Phage Purification/Fallexp/Period3/Dailylog

From 2013.igem.org

(Difference between revisions)
Line 67: Line 67:
: 2 microL DNA ladder in first well
: 2 microL DNA ladder in first well
: 2 microL stain and 5 microL sample, mix and put in well
: 2 microL stain and 5 microL sample, mix and put in well
 +
: Run at 130 V for
We place the samples in the order: DNA ladder, 297/298 W M, 301/302 W M, 311/312 W M, 313/314 W M
We place the samples in the order: DNA ladder, 297/298 W M, 301/302 W M, 311/312 W M, 313/314 W M

Revision as of 22:02, 23 October 2013


Phage Purification September - October Notebook: October 21- 27 Daily Log



Phage Purification
March-April
May-June
July-August
September-October



<< Previous Next >>


10/21/13

-Today we ran PCR on T4 wild type and mutant phage to determine the sequence differences in the capsid proteins.

- 10.21 T4 PCR

AB DL AC


10/23/13

-Ran a gel on the PCR we did last time.

-Gel
100 mL TAE 1x
1 g regular agarose
2 drops ethidium bromide
Combine and melt TAE and agarose
Cool and add 2 drops ethidium bromide
Allow gel to form with 14 well mold (20 minutes in the fridge)
-Preparing machine
Fill machine with TAE buffer until it covers gel
2 microL DNA ladder in first well
2 microL stain and 5 microL sample, mix and put in well
Run at 130 V for

We place the samples in the order: DNA ladder, 297/298 W M, 301/302 W M, 311/312 W M, 313/314 W M W=wildtype M=mutant


AB DL AC


<< Previous Next >>