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Revision as of 19:07, 19 July 2010 (view source) Karpadillo (Talk | contribs) (→Karina's Notebook) ← Older edit		Revision as of 19:07, 19 July 2010 (view source) Karpadillo (Talk | contribs) (→Karina's Notebook) Newer edit →
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	*run at 95 V for about an hour <br/>		*run at 95 V for about an hour <br/>
-	**note sizes of plasmids/inserts <br/><br/>	+	!!note sizes of plasmids/inserts <br/><br/>
	GFP --> pSB1A2 (<br/>		GFP --> pSB1A2 (<br/>
	RFP --> pSB2K3<br/>		RFP --> pSB2K3<br/>

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Revision as of 19:07, 19 July 2010

Meeting Minutes

[http://docs.google.com/present/edit?id=0Ae31et9w_tAhZGZyc3R2ejJfOGNnY2drMmZz&hl=en&authkey=CPHGzfIB Weekly Leader Presentation: Karina]

Agenda

Karina's Notebook

Today's Goal: Digest GFP, RFP, and Terminators. Will do (GFP + T) and (RFP + T) ligations on monday.

Part #'s:

• GFP: E0040 (cut at S and P)
  
• RFP: E1010 (cut at S and P)
  
• Term: B1006 (cut at X and P)
  
  

Recipe

• 12.0 uL DNA
  
• 1.0 uL each enzyme
  
• 5.0 uL NEB buffer 2
  
• 5 uL BSA (10x)
  
• Sterile H20 to fill up to 50 uL
  
  

Mix and put 37º waterbath for 2 or more hours.

Making Gel
To make 50 mL of 0.8% agarose gel, add:

• .4 g agarose
  
• 50 mL TAE (1x)
  
• 10 uL EtBr
  
  

Loading the Gel

• add 10 uL loading dye (6x) to digests
  
• add 40 uL of dye + digests to wells
  
• don't forget to include wells with controls! (uncut plasmids)
  
• load 10 uL ladder
  
• run at 95 V for about an hour
  

!!note sizes of plasmids/inserts

GFP --> pSB1A2 (
RFP --> pSB2K3