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	<ul>The procedure consists of three basic steps:		<ul>The procedure consists of three basic steps:
-	■ Preparation and clearing of a bacterial lysate	+
-	■ Adsorption of DNA onto the QIAprep membrane	+	<li> Firstly, the cells are cultured overnight and spun down and resuspended to a concentrated volume. The resuspension solution contains  RNAase which degrades all the RNA to minimize the contamination and possible interaction of RNA with the plasmidsSubsequently this concentrated volume of the cells are lysed using an alkaline lysis buffer. This breaks open the cell wall and membrane to spill out the inner composition of the cell. Following the lysis, the cell is neutralized using an acidic solution which also serves the purpose of creating a high salt environment with ions. Following this step, the cells are transfered to a silica column which binds DNA along with some endonucleases but allows everything else to pass through. A final wash step is done to ensure that the endonuclease is washed off leaving mostly the DNA. However, this can have some RNA contamination left in it. Then the column is washed with 50-100 µL and speced to measure the concentration. </ul>
-	■ Washing and elution of plasmid DNA	+
-	All steps are performed without the use of phenol, chloroform, CsCl, ethidium bromide,	+
-	and without alcohol precipitation.</ul>	+
	<h3>Tips</h3>		<h3>Tips</h3>

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Revision as of 07:10, 26 October 2010

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Taq Polymerase Chain Reaction

Theory

PCR amplifies a portion of DNA, as bounded by specific primers. The process mimics the replication of DNA in a regular cell.

1. First, the two strands of the template DNA are separated (denatured) at 95°C, which is a high enough temperature to break the hydrogen bonds between the base pairs.
2. Next comes the annealing of the primers. The annealing temperature is extremely specific to the primer being used. There are many programs out there that can help you determine the annealing temperature of the primer such as BLAST primer and GCK.
3. Then, at 72°C, the Taq polymerase extends the annealed primer to create a copy of the DNA template. The process repeats. Note: you can use Pfu or other polymerases with exonuclease activity in order to ensure that there are no mutations are added.

Primers are short pieces of DNA (approximately 20-30 bases long) that are complementary to the base strand. Since polymerase can only attach an incoming 5' nucleotide to an existing 3' end, a starting point for the polymerase to "attach to" has to exist. This is the end of the primer. As a result, the portion bound between the two primers is amplified.

Taq polymerase is harvested from bacteria that live in hot springs, and it is used because it is functional at relatively high temperatures. Its optimal functioning temperature is at 72°C. Otherwise, the denaturation temperatures (at 95°C) will destroy the polymerase and cause the PCR to fail. MgCl₂ is a salt that allows Taq polymerase to function.

Because polymerase can only go so fast, you should allow approximately 1 minute for every 1000 base pairs to be amplified, to ensure that the strand is fully copied before the cycle repeats. Step 5 is the final extension time, which ensures that all strands are extended completely. Then the PCR product can be held as long as you need it to be held at 4°C.

Tips

• For the Master Mix, you should add water in two portions (half added before all other reagents and half added after all other reagents).
• Make sure you spin down the mixture with centrifuge or microfuge before you add Taq

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Preparation of Competent cells

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Bacterial Transformation

You may leave the cells shaking for longer than an hour but not overnight. Leaving the cells in the shaker for about 2-4 hours allows the cells to grow and recover well. This gives high transformation efficieny with lots of colonies.

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Restriction Digest

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Ligation

Quick ligase is expensive, you can use quick ligase buffer with regular T4 ligase and ligate at room temperature for 15-20 minutes and it will do the same trick!

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Miniprep Plasmid Preparation (using GenElute)

Theory

Miniprepping allows one to extract plasmid DNA from bacteria. The principle behind this includes alkaline lysis followed by a silica column adhesion and elusion using water/ respective buffer. For example the QIAgen kit works like Principle The QIAprep miniprep procedure is based on alkaline lysis of bacterial cells followed by adsorption of DNA onto silica in the presence of high salt (1). The unique silica membrane used in QIAprep Miniprep Kits completely replaces glass or silica slurries for plasmid minipreps.

The procedure consists of three basic steps:
• Firstly, the cells are cultured overnight and spun down and resuspended to a concentrated volume. The resuspension solution contains RNAase which degrades all the RNA to minimize the contamination and possible interaction of RNA with the plasmidsSubsequently this concentrated volume of the cells are lysed using an alkaline lysis buffer. This breaks open the cell wall and membrane to spill out the inner composition of the cell. Following the lysis, the cell is neutralized using an acidic solution which also serves the purpose of creating a high salt environment with ions. Following this step, the cells are transfered to a silica column which binds DNA along with some endonucleases but allows everything else to pass through. A final wash step is done to ensure that the endonuclease is washed off leaving mostly the DNA. However, this can have some RNA contamination left in it. Then the column is washed with 50-100 µL and speced to measure the concentration.

Tips

• When you are spec-ing your DNA, make sure you use the elution water/ buffer as your blank.
• When spinning your DNA after lysing and neutralization you can spin for 15-20 minutes. This allows the debris to stick to the side of the tube allowing transferring the supernatant with the plasmid much easier and contaminant free.

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Agarose Gel Electrophoresis

Tips

If you are looking for a big band higher up in the ladder, run the gel at a higher voltage for a shorter period of time. Ethidium bromide wash if necessary. You don't always have to prepare the 20 μL of solution, you can add appropriate amount of DNA usually 3 μL and then add 2 μL dye and just run teh entire mixture in the gel. Make sure you are careful and there are no bubbles in the well, or in your pipette tip. That would move the DNA out of the gel.

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Making of Agarose Gels

Tips

• When looking for large bands, make gels that are higher than one percent and run at a higher voltage, do the opposite for smaller sized bands.

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Rehydration of Registry DNA

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Construction Technique

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Overnight Cultures

Tips

• Make a control tube with your respective antibiotic. Do not put a colony in there and see if there is any growth. This will ensure that your antibiotics are working.

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Glycerol Stock Preparation

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LB Agar Plate Preparation

Tips

• Tape up plate sleeves if planning to reuse the sleeves

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QIAprep Spin Miniprep Kit

Tips

• Drying for 2 minutes instead of 1 minute can ensure that all of the wash solution is removed
• When doing the aliquot step, put the pipette tip directly on the filter and eject in the center of the filter
• Wait 15 minutes after adding the water onto the filter in the aliquot step

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Gel Extraction

Tips

• Shorten melting time and alternate between 30 seconds in heat plate and 30 seconds in vortex and look at solution in light to ensure gel is melted.
• Use clear 1.5 tubes so that its possible to observe the colour change caused Binding Buffer(XP2) when the pH is too high or too low
• Dry step after the addition of Binding Buffer(XP2) could help separate the SPW buffer and Binding Buffer(XP2) stages.
• Shorten the length of spin and increase the rpm for the addition of binding buffer and SPW steps and increase to 2 minutes for drying stages
• Ensure that the spin column is dry before transferring into the clean 1.5 mL tube
• You may use isopropanol to dilute the QG solution after the gel is melted. This increases the yield of DNA

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PCR Purification

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