Team:Newcastle/22 June 2010

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'''22 June 2010'''
 
===Aims===  
===Aims===  
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The aim of today's Lab practice was to extract the plasmids for GFP and RFP, digest the 2 plasmids and extract the 2 inserts and 1 of the backbones (vector)from a gel. From this a ligation was set up.   
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The aim of today's Lab practice was to extract the plasmids for GFP and RFP, digest the 2 plasmids and extract the 2 inserts and 1 of the backbones (vector)from an agarose gel. From this a ligation was set up.   
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===Equipment List===
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===Materials and Protocol===
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For today's Lab pratice we required:  
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====QIagen Miniprep Kit Using a Microcentrifuge for Plasmid Extraction====
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Please refer to: [[Team:Newcastle/Qiagen Minipreps|Qiagen Minipreps]] for materials required and protocol.
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* Broth cultures from yesterday
 
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* Solutions for Minipreps( plasmid and gel extraction,digest and ligation)
 
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* Buffers
 
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* Agarose gel
 
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* Microwave
 
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* Restriction enzymes
 
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* Gloves(for handling the gel)
 
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* Scalpel
 
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* Scales
 
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* Transilluminator
 
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* Nanodrop
 
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===Qiagen miniprep: Plasmid extraction(Summary)===
 
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The 5ml culture set up yesterday was pelleted down using the microcentrifuge, the pellet was resuspended in buffer P1.
 
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Lysis buffer P2 was used to release the DNA from the cell (this buffer contains RNAse to help reduce RNA contamination). PE buffer containing ethanol was used as a wash. We lysed the cells for 1 minute, gently inverting the tube. We neutalised  the lysis with N3 buffer and centrifuged for 10minutes, only the '''plasmid DNA was left in suspension'''. The DNA was eluted at low salt concentration through a column membrane.
 
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====Miniprep Kit Using a Microcentrifuge:Step by step====
 
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The Miniprep Kit is used to extract plasmid, which is the first thing that we did.
 
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# Resuspend pelleted bacterial cells in 250 μl Buffer P1 and transfer to a microcentrifuge tube.
 
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# Add 250 μl Buffer P2 and mix throughly by inverting the tube 4-6 times.
 
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# Add 350 μl Buffer N3 and mix immediately and thoroughly by inverting the tube 4-6 times.
 
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# Centrifuge for 10 min at 13,000 rpm in a table-top microcentrifuge.
 
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# Apply the supernatant to the QIAprep spin column by decanting or pipetting.
 
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# Centrifuge for 30-60s. Discard the flow-through.
 
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# Recommended: Wash the QIAprep spin column by adding 0.5 ml Buffer PB and centrifuging for 30-60s. Discard the flow-through.
 
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# Wash QIAprep spin column by adding 0.75 ml Buffer PE and centrifuging for 30-60s. 
 
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# Discard the flow-through, and centrifuge for an additional 1 min to remove residual wash buffer.
 
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# To elute DNA, place the QIAprep column in a clean 1.5 ml microcentrifuge tube. Add 50 μl Buffer EB or water to the center of each QIAprep spin column, let stand for 1 min, and centrifuge for 1 min.
 
===Digest===
===Digest===
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Please refer to: [[Team:Newcastle/Restriction digests| Restriction digests]] for materials required and protocol.
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Cut with restriction enzyme ''Eco''R1 and ''Pst''1 1 μl of each, the prefix and suffix of the BBa_04450 biobrick.
 
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10*buffer ... so 3 μl in 30μ1 therefore we can have 25μ1 of DNA
 
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Also no more than 10% Glycerol in the enzyme solution or the reaction would be inhibited.
 
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# 20 μl solution should be made in total: 15 μl plasmid (with GFP/RFP), 1 μl EcoRI, 1 μl PstI, 2 μl Buffer (10x), 1μl water. '''NOTE:''' Digestive enzymes should never exceed 10% of the total volume.
 
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# Add the reagents in this order: plasmid, water, buffer, enzymes.
 
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# Centrifuge for a few seconds to make sure that the mixture is at the bottom.
 
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# Heat block for 2 hours at 37 degrees C.
 
===Gel extraction===
===Gel extraction===
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Please refer to: [[Team:Newcastle/Gel extraction| Gel extraction]] for materials required and protocol.
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Gel electrophoresis can be used to separate DNA, RNA, or protein molecules by molecular weight using an electric field applied to a gel matrix
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====Agarose gel====
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====Agarose Gel Electrophoresis====
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Please refer to: [[Team:Newcastle/Gel electrophoresis| Gel electrophoresis]] for materials required and protocol.
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Agarose gel is used for DNA seperation. 1% agarose(1g of agarose in 100 ml of TAE buffer) is used because it is suitable for most kilobase pairs of DNA. We used 60ml for our gel. We used SafeView dye (3 μl) to bind the DNA so that the DNA is visible. We used TAE buffer and boiled the mixture in a microwave to melt it. We then let it cool and poured it into the tank to set( Wait for 30 min to allow the gel to harden).
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====Electrophoresis====
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Transfer harden gel into the gel tank and add TAE buffer until the gel is completely submerge
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Depending on the nature of the sample, 3μl of GeneRuler™ 1kb Plus DNA Ladder was used for analysing DNA
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Loading buffer was then added together with the sample before loading onto the gel matrix
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Run gel at 90V until separation is achieved and visualize using the gelDoc
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In lane one we loaded the molecular marker 5μl. In lane three we loaded the digested RFP plasmid. In lane five we loaded the digested GFP plasmid. In lane eight we loaded 5μl RFP plasmid and 1μl sample buffer. Lanes two, four, six and seven are empty.
 
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Revision as of 20:23, 21 October 2010

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Contents

Aims

The aim of today's Lab practice was to extract the plasmids for GFP and RFP, digest the 2 plasmids and extract the 2 inserts and 1 of the backbones (vector)from an agarose gel. From this a ligation was set up.

Materials and Protocol

QIagen Miniprep Kit Using a Microcentrifuge for Plasmid Extraction

Please refer to: Qiagen Minipreps for materials required and protocol.


Digest

Please refer to: Restriction digests for materials required and protocol.


Gel extraction

Please refer to: Gel extraction for materials required and protocol.


Agarose Gel Electrophoresis

Please refer to: Gel electrophoresis for materials required and protocol.

Newcastle lab 1.jpeg
Newcastle lab 2.jpeg
Newcastle lab 3.jpeg

Cut gel out

Newcastle lab 4.jpeg
Newcastle lab 5.jpeg
Newcastle lab 6.jpeg

We cut the inserts which were about 900bp and we use the backbone from the RFP plasmid.

QIAquick Gel extraction kit

Newcastle lab 7.jpeg
Newcastle lab 8.jpeg

The DNA fragments are cut from the agarose gel with a scalpel. Three parts of QG buffer is added to one part of gel and the mixtures are dissolved at the temperature of 50°C. The tubes are vortexed every 2-3 minutes to help dissolve the gel. 1 part of isopropanol is added to the sample and mix. The microcubes were spinned in the microfuge for 1 minute.

QIAquick gel extraction microcentrifuge protocol

  1. Excise the DNA fragment from the agarose gel with a clean, sharp scalpel
  2. Weight the gel slice and add 3 volumes of buffer QG to 1 volume of gel (100 mg ~ 100 µl)
  3. Incubate at 50°C and invert the tube gently at regular intrerval until the gel has completely dissolved
  4. After the gel has dissovled completely, check that the color of the mixture is yellow
  5. Add 1 gel volume of isopropanol to the sample and mix
  6. Place a QIAquick spin column in a 2 ml collection tube
  7. To bind DNA, apple the sample to the QIAquick column and centrifuge for 1 min
  8. Discard the flow through and place the QIAquick column back into the same tube (Maximum volumn is 750ul)
  9. Add 0.5 ml of Buffer QG to QIAquick column and centrifuge for 1 min and discard the flow through and place the QIAquick column back into the same tube
  10. To wash, add 0.75 ml of Buffer PE to QIAquick column and centrifuge for 1 min and place the QIAquick column back into the same tube
  11. Centrifuge the column for a further 1 min
  12. Transfer the column into a clean 1.5 ml micriocentrifuge tube
  13. To elute DNA, add 30 µl of Buffer EB to the center of the QIAquick membrane and allow to stand for 1 min
  14. Centrifuge the column for 1 min and transfer the eluate to a clean 1.5 ml micriocentrifuge tube

Weighing

All gel extractions weighed 0.3g.

Set up ligation

Reagents 1:3(μl) 1:5(μl) Vector(μl)
V 0.8 0.8 1
G 2.7 4
R 5.4 7.7
LT4 1 1 1
LB 1.1 1.5 1
H2O 0 0 7
Total Volume 11.0 15.0 10.0

Transformation protocol

  1. Thaw a 200µl aliquot of the desired strain of E. coli and add the transforming DNA (10 ng of vector DNA in 10 µl). Incubate for 45 min at 42°C.
  2. Heat-shock the cells for 120 secs, and place on ice again for 3-4 min.
  3. Add 1ml of LB broth and incubate the cells at 37°C for 1-15 hr in a water bath with gentle shaking.
  4. Plate out 100-200 µl/plate on LB (agar at 1.5%), containing the appropriate selection markers.
  5. Incubate plates overnight at 37°C.

Nanodrop Protocol

Nanodrop can be used to measure the DNA, RNA and protein

  1. Select Nanodrop program from the desktop
  2. To clean Nanodrop, add a drop of water on the spectrometer and press blank
  3. After cleaning, wipe the water off
  4. To equalizen the equipment, add 3 μl of the buffer used in the sample and press blank
  5. Wipe the buffer off
  6. To measure sample, add 3 μl of the sample and press measure
  7. If dealing with multiple samples, clean the equipment with water at regular intervals
  8. After measurement, clean the equipment with a drop of water on the spectrometer and press blank


Newcastle nanodrop 1.jpeg
Newcastle nanodrop 2.jpeg
Newcastle nanodrop 3.jpeg

Outcome

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