Minnesota/10 July 2008

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Revision as of 16:18, 10 July 2008

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1. Dephosphorylation: Continued with double digestion base vector product from 07-09-2008. Used Antartic phosphoylase to dephosphorylate the base vector. Want to dephosphorylate the base vector to prevent it from closing - want it to stay a linear digested product. After dephosphorylation, the base vector was then incubated @ 37C for 30 minutes. Sample was then placed in a heat bath @ 65C for 15 minutes to inactivate enzyme (phosphotase).

Gene	10x Buffer	DNA	Phosphotase
Base Vector	5.6uL	50.0uL	1.0uL

NOTE: Total volume in dephosphorylation = 56.6uL

2. Run RXN model on Calhoun (super computer).

3. Dilute base vector culture, allow to grow, then miniprep, then streak plates and make base vector glycerol stocks.

4. Autoclave dishes

5. Ligation: Follow table below. When ligation is completed, incubate products @16C for 1 hour. Heat inactivate DNA ligase (enzyme) @ 65C for 15 minutes.

Reagent	Volume in uL
10x Buffer	2.0uL
H20	20.0uL
Vector
DNA
T4 DNA Ligase	1.0uL

@@ Line 27: / Line 27: @@
 |2. '''Run RXN model on Calhoun''' (super computer).
 |-
-|3. Diluate base vector culture, allow to grow, then miniprep, then streak plates and '''make base vector glycerol stocks.'''
+|3. Dilute base vector culture, allow to grow, then miniprep, then streak plates and '''make base vector glycerol stocks.'''
 |-
 |4. '''Autoclave dishes'''
 |-
-|5.
+|5. '''Ligation''': Follow table below. When ligation is completed, incubate products @16C for 1 hour. Heat inactivate DNA ligase (enzyme) @ 65C for 15 minutes.
+|-
+|}
+{|border="1" align="left"
+|-
+!| Reagent !!Volume in uL
+|-
+|10x Buffer ||2.0uL
+|-
+|H20 ||20.0uL
+|-
+|Vector ||
+|-
+|DNA ||
+|-
+|T4 DNA Ligase || 1.0uL
+|-
+|}