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

(Difference between revisions)

Revision as of 21:40, 23 October 2013

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

Phage Purification

March-April

10/21/13

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

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

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

@@ Line 53: / Line 53: @@
 <br>
+<font size="4"> '''10/23/13''' </font>
+-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
+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
+<br>
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