The primers will come dry, in small tubes. They are stable at room temperature. As soon as you add water, you will want to keep the primers on ice. You will need to make a 200 millimollar stock of the primers. I also recommend making a working stock as well.
To make the 200 mm stock, find the volume in nanomoles and multiply by 5.
Gene1-1F - 29.4 nm x 5 = 147 ul
Gene1-1R - 35.1 nm x 5 = 175.5 ul
Gene2-1F - 29.6 nm x 5 = 148 ul
Gene2-1R - 29.2 nm x 5 = 146 ul
Take that amount of microliters per tube and add Molecular Grade ddH20 to the tube. You now have a 200 mm stock.
Vortex the tube to mix them. Spin them down in the centrifuge.
For regular PCR, the concentration should be at 20 mm. For RT-PCR, you want it to be at 10 mm.
Using the C1V1=C2V2 equation : (200 mM) x = (20 mM) (100 ul)
x = 10 ul
You want a working stock of 100 microliters. You can put both the forward and reverse primer into your working stock. So 10 ul/2 = 5 ul of the forward primer and 5 ul of the reverse primer.
Add 90 ul of Molecular grade water
5 ul of forward primer
5 ul of reverse primer
Total of 100 ul working stock
Vortex the tube to mix them. Spin them down in the centrifuge.
You want to keep both the long-term 20 mm stock and the working stock (F+R primers) on ice, or in that -20 to -30 C freezer.
Next, you want to create a Master Mix solution. You want the number of reactions + 10% room for error. Total volume for each well (each primer being tested) is 20 ul. If you are testing 5 genes, then that would be 5 reactions (or 5 wells). So take the Mastermix recipe and times it by number of reactions and 1.1 for each of the elements.
Do not add the primer working stocks to the Mastermix. If you are using different templates, say cDNA from mouse and cDNA from frog. DO NOT ADD IN THE TEMPLATE yet to the Mastermix. However, if you are testing genes for the same species, with the same template you can add the template to the Mastermix. Let's assume that all the 5 genes I am testing are for the same species. I will add 22 ul of template to the Mastermix solution.
Next, get some tiny PCR tubes (and lids). Remember, the desired volume for each PCR tube is 20 ul (For regular PCR. For RT-PCR, you want 10 mm). You want to add 19.2 ul of Mastermix to each tube. Then you want to add 0.8 ul of each primer working stock (changing pipette tips each time!!). Then you total volume is 20 ul.
RUNNING THE PCR MACHINE
Each PCR machine varies, but here is the general procedure:
Put the tubes in. Tighten the lid.
-20 ul volume
-Last step should run at 4C forever.
Check with your lab about the specific program you want to run (with temps, times, and cycles). Our PCR machine has a program pre-set.
Here is the program I use for PCR.
5 minutes 94 degrees (x 1 cycle)
1 minute 94 degrees (x 40 cycles)
1 minute 55 degrees (x 40 cycles)
2 minutes 72 degrees (x 40 cycles)
7 minutes 72 degrees (x 1 cycle)
15 minutes 4 degrees (x 1 cycle)
(set on 4 degrees forever, if you want to leave it overnight)
If you want to know what occurs during each step (of the denaturation, annealing, and extension process), check out NCBI's explanation.
RUNNING A GEL
Right before you want to run the gel, add a loading dye to each well. I use a 6x loading dye, but it needs to be at 1x. I use the C1V1=C2V2 formula to solve for x:
(6x)(y) = (20 ul)(1x)
y = 3.333 ul
I want to add 3.3 ul of 6x loading dye to each tube. This will turn the solution from clear to blue. Spin the tubes down.
|Mastermix + Primer and Templates in PCR reaction tubes|
RUNNING A GEL
First you want to make the 1-2% agarose gel.
Depending on your gel casting tray size, you will need different volumes. I am running a small gel and my casting tray holds about 75 ml. To test how much volume it holds, just pour water in from a graduated cylinder to find out. I am going to make slightly more than I need to be safe. A clamp is used on the gel casting tray. Put the comb in. This will create wells when you pour the agarose in.
|Gel Casting tray|
If I want 82 mls of agarose gel mix, I will use 0.82 grams of agarose powder.
I add the powder to 82 mls of Borax. Next I want to microwave it, until it boils. DON'T LET IT BOIL OVER! You may have to stop and wait a few times, until all the particles are dissolved. The solution below needs to be microwaved longer.
|1% Agarose Gel solution|
You want the solution to be clear.
When the solution is clear, wait for the agarose gel solution to cool down. When it is room temp, you want to add Ethidium.
Ethidium is a dangerous chemical and is usually kept in a safe place, stored at room temperature. For a small gel, use 1-2 ul of Ethidium. For a large gel, use 5 ul. In our lab, we use a pipetter reserved for the Ethidium only and kept in a cleared out area assumed to be ethidium-dirty.
Swirl the bottle to mix up the Ethidium into the agarose gel. Pour the gel in the gel casting tray, as pictured above. It should be 15 minutes or longer for the gel to congeal. If you wait too long it will solidify in the bottle.
MAKE SURE THAT NO BUBBLES ARE NEAR THE COMB!
When the gel is solid, you can unclamp the casting tray and carefully remove the tray with the agarose gel in it. It should be rectangular and jelly-like.
Move the gel to the gel electroporesis box.
Pour in Borax to cover the tray. Don't fill it past the MAX line.
Pull the comb out. If you place a dark sheet under the box, you should be able to see square wells. This is where you will pipette your mix into.
For a large gel, you want to put 8-10 ul of each Mastermix+Template+primers+loading dye into each well. For smaller gels, 2-4 ul might be adequate. If you run your gel and get blobs and trails, it may be because there is too much DNA. Cutting the concentration will help.
Use a different pipette tip each time!
In the peripheral wells, you want to use a DNA ladder. I use a 100 bp ladder and a 1000 bp ladder. This will allow you to gauge how large your product is compared to a reliable measure of size.
In general, you can use about 5 microliters for the 100 bp ladder and 2-3 microliters for the 1000 bp ladder.
|Wells are filled in the gel electroporesis box|
Write down which primer is in each well!
Put the cover onto the electroporesis, matching black to black and red to red.
Turn the gel electroporesis machine on. I use a setting of 110, then start it.
You should see bubbles coming out of the anodes. Let your gel run for 20-45 minutes. You want them to run down 75% the length of your gel. If you let it run too long, it will run right off your gel!
A finished gel should look like the one below:
Note: I disposed of my gel in a special hazardous waste ethidium bromide container.
Next, I photograph the gel using a special Gel-Doc machine that uses Trans-UV to image. I invert the image when exporting as a .TIFF file to get the picture below:
INTERPRETING A GEL
Recall that bigger fragments move more slowly and smaller fragments move faster. To give you an idea of relative size, the DNA ladders (100 bp and 1000 bp) are used. Since the fragments will run from the negative electrode (black) to the positive electrode (red), the slower fragments will be closer to the starting point. Read the ladder from the bottom up. See below. The brighter bands are 500 and 1000.
You want your band to be a single, bold band. Multiple bands can indicate contamination or non-specific binding of your primers.
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