Team:Newcastle/22 June 2010

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'''Tuesday'''
 
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===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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===Equipement List===
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==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 an agarose gel. From this a ligation was set up. 
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For today's Lab pratice we required:
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==Materials and Protocol==
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* Broth cultures from yesterday
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===QIagen Miniprep Kit Using a Microcentrifuge for Plasmid Extraction===
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* Solutions for Minipreps( plasmid and gel extraction,digest and ligation)
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Please refer to: [[Team:Newcastle/Qiagen Minipreps|Qiagen Minipreps]] for materials required and protocol.
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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.
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===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.
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===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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|[[Image:Newcastle_lab_1.jpeg|thumb]]
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|[[Image:Newcastle_lab_1.jpeg|thumb|Dr Wendy demostrating how to use gel electrophoresis machine]]
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|[[Image:Newcastle_lab_2.jpeg|thumb]]
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|[[Image:Newcastle_lab_2.jpeg|thumb|Gel tank]]
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|[[Image:Newcastle_lab_3.jpeg|thumb]]
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|[[Image:Newcastle_lab_3.jpeg|thumb|Deena pouring hot molten gel]]
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|}
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{|
{|
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|[[Image:Newcastle_lab_4.jpeg|thumb]]
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|[[Image:Newcastle_lab_4.jpeg|thumb|Putting the gel on the geldoc]]
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|[[Image:Newcastle_lab_5.jpeg|thumb]]
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|[[Image:Newcastle_lab_5.jpeg|thumb|Preparing to cut the gel]]
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|[[Image:Newcastle_lab_6.jpeg|thumb]]
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|[[Image:Newcastle_lab_6.jpeg|thumb|Gel illuminated by the UV light which is emitted by the geldoc]]
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We cut the inserts which were about 900bp and we use the backbone from the RFP plasmid.
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We cut the inserts which were about 900bp and we use the backbone from the plasmid consisting ''rfp''.
====QIAquick Gel extraction kit====
====QIAquick Gel extraction kit====
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{|
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|[[Image:Newcastle_lab_7.jpeg|thumb]]
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|[[Image:Newcastle_lab_7.jpeg|thumb|Phil cutting the gel]]
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|[[Image:Newcastle_lab_8.jpeg|thumb]]
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|[[Image:Newcastle_lab_8.jpeg|thumb|Transferring the cut gel part into a 2 ml microfuge tube]]
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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.
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==Set up ligation==
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====Weighing====
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All gel extractions weighed 0.3g.
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===Set up ligation===
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{|border=1
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==Transformation protocol==
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Please refer to: [[Team:Newcastle/Transformation of E. coli|Transformation of ''E. coli'']] for materials required and protocol.
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===Nanodrop Protocol===
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==Nanodrop Protocol==
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Please refer to: [[TeamNewcastleNanoDrop Spectrophotometer| Nanodrop Spectrophotometer]] for materials required and protocol.
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Nanodrop can be used to measure the DNA, RNA and protein
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# Select Nanodrop program from the desktop
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# To clean Nanodrop, add a drop of water on the spectrometer and press blank
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# After cleaning, wipe the water off
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# To equalizen the equipment, add 3 μl of the buffer used in the sample and press blank
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# Wipe the buffer off
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# To measure sample, add 3 μl of the sample and press measure
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# If dealing with multiple samples, clean the equipment with water at regular intervals
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# After measurement, clean the equipment with a drop of water on the spectrometer and press blank
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{|
{|
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|[[Image:Newcastle_nanodrop_1.jpeg|thumb]]
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|[[Image:Newcastle_nanodrop_1.jpeg|thumb|A typical curve to be achieved from a nanodrop spectrophotmeter]]
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|[[Image:Newcastle_nanodrop_2.jpeg|thumb]]
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|[[Image:Newcastle_nanodrop_2.jpeg|thumb|Phil analyzing a sample on the nanodrop machine]]
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|[[Image:Newcastle_nanodrop_3.jpeg|thumb]]
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|[[Image:Newcastle_nanodrop_3.jpeg|thumb|Analyzed data on the screen]]
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==Outcome==
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{| style="color:#1b2c8a;background-color:#0c6;" cellpadding="2" cellspacing="1" border="1" bordercolor="#fff" width="62%" align="center"
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!align="center"|[[Team:Newcastle|Home]]
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!align="center"|[[Team:Newcastle/Team|Team]]
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!align="center"|[https://igem.org/Team.cgi?year=2010&team_name=Newcastle Official Team Profile]
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!align="center"|[[Team:Newcastle/Project|Project]]
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!align="center"|[[Team:Newcastle/Parts|Parts Submitted to the Registry]]
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!align="center"|[[Team:Newcastle/Modelling|Modelling]]
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!align="center"|[[Team:Newcastle/Notebook|Notebook]]
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!align="center"|[[Team:Newcastle/Safety|Safety]]
|}
|}
{{Team:Newcastle/footer}}
{{Team:Newcastle/footer}}

Latest revision as of 20:42, 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.

Dr Wendy demostrating how to use gel electrophoresis machine
Gel tank
Deena pouring hot molten gel

Cut gel out

Putting the gel on the geldoc
Preparing to cut the gel
Gel illuminated by the UV light which is emitted by the geldoc

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

QIAquick Gel extraction kit

Phil cutting the gel
Transferring the cut gel part into a 2 ml microfuge tube

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

Please refer to: Transformation of E. coli for materials required and protocol.

Nanodrop Protocol

Please refer to: Nanodrop Spectrophotometer for materials required and protocol.


A typical curve to be achieved from a nanodrop spectrophotmeter
Phil analyzing a sample on the nanodrop machine
Analyzed data on the screen

Outcome

Home Team Official Team Profile Project Parts Submitted to the Registry Modelling Notebook Safety
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