Team:Newcastle/12 July 2010

From 2010.igem.org

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===Aims===
===Aims===
The aim of todays Lab session was to perform the following(see summary) to isolate ''lacI''.  
The aim of todays Lab session was to perform the following(see summary) to isolate ''lacI''.  
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[[Image:P7120450.JPG|300px|thumb|right]]
Summary:
Summary:
# Colony PCR
# Colony PCR
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# Miniprep PCR- of colonies that worked
# Miniprep PCR- of colonies that worked
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[[Image:P7120450.JPG|300px|thumb|right]]
 
===Equipment===  
===Equipment===  

Revision as of 15:45, 21 July 2010

Monday

Contents

Aims

The aim of todays Lab session was to perform the following(see summary) to isolate lacI.

P7120450.JPG

Summary:

  1. Colony PCR
  2. Streak plate
  3. Miniprep PCR- of colonies that worked


Equipment

  • PCR reagents
  • Agar plates
  • Gloves
  • Wire loop

Colony PCR

Of the 11 plates with colonies grown 7 were used for colony PCR and Streak plating. Colony PCR is less accurate than the mini prep however results can be seen quicker whereas the miniprep has a 1 day wait. The colonies selected selected were satellite colonies because ampicillin degraded???

7 Tubes were labelled 1-7 (+ a control)

The quantities for the PCR are as follows:

P7120427.JPG
  • 1microlitre Template
  • 0.25 microlitre GoTaq Polymerase
  • 2.5 microlitre forward primer
  • 2.5 microlitre reverse primer
  • 1 microlitre dNTP (10molar stock)
  • 10.0 microlitre 5times GoTaq buffer
  • 32.75 microlitre deionised H20

Note There are 2 possible reasons for red colonies formed:

  1. Partial digest- rejoins without insert
  2. with insert

We need to tell the difference between the two.

Note PCR is best when everything is kept on ice!

P7120427.JPG
P7120450.JPG


Note Melting temperatures of primers is important and can have a big effect on the product formed (Temperature used see Thursday)

Spread Plates

P7120408.JPG
P7120409.JPG
P7120418.JPG
P7120413.JPG

Tommorrow

We are going to take one of the colonies that have worked and possible a whole plasmid prep.