Team:StanfordBrownSpelman/Lab

Using the Autoclave
Interns can’t. Ask someone with a hard badge. Typical runs take about an hour, but could be two hours if the boiler isn’t warmed up.

Media
Most of the time you'll autoclave the media after putting it together, although certain chemicals (vitamins, antibiotics) need to be added after to prevent degradation.

LB: Use for E. coli
For 500mL, add:
5g Tryptone (or Peptone)
2.5g Yeast Extract
5g NaCl
7.5g Agar (if making plates)
Into 500ml of deionized water

AM (Acetobacter Media): Use for G. hansenii
For 500mL, add:
10g Glucose
2.5g Tryptone (or Peptone)
2.5g Yeast Extract
1.35g Na₂HPO₄
0.75g Citric Acid
7.5g Agar (if making plates)
Into 500ml deionized water

Antibiotic Stocks
We usually make our liquid stocks of antibiotics at 1000X, so that you add 1μl/mL to whatever media you are using. While the desired working concentration might change based on the plasmid, here are the stock concentrations we usually use for common antibiotics:
Chloramphenicol: 34mg/mL (100% EtOH)
Ampicillin: 100mg/mL (50% EtOH)
Kanamycin: 20mg/mL (H20 only)
Neomycin: 50mg/mL (H20 only)
Tetracycline: 15mg/mL (50% EtOH)
You'll want to make these by filter sterilizing; you cannot autoclave antibiotics. We typically store them in 1mL aliquots in a -20C or -30C freezer. Those stocks made with ethanol will not freeze. Those in water only will require thaw time.

Plates
Basics
Using any typical media recipe, add 1.5% agar (15g/L) to the mixture before autoclaving
After removing from autoclave, let cool until it is cool enough to hold for several seconds comfortably (otherwise the media will be too hot and break down the antibiotic)
Add the appropriate amount of antibiotic
Pour enough media into each petri dish to just cover the bottom
E. coli grows on the surface, so the agar layer shouldn’t be thick
Since the dishes come in sleeves of 25, it is usually good to make 500mL of the medium

Keeping Them Sterile
We have a UV hood that we usually make plates in
Gather everything you'll need to make the plates (empty petri dishes, pipette, pipette tip, sharpie, etc) and wipe down with 70% ethanol before placing in the hood
Sterilize for ~5-10min by exposing to UV lamp

Standard Molecular Workflow
Note: PCR is its own huge beast, so it's been given its own section following this one

Liquid Culture
Inoculation: Pipette tips work great for swiping or stabbing a colony
Media: LB works great for both E. coli and B. subtilis
Temperature: 37°C works fine for both E. coli and B. subtilis
Shaker speed: 250 RPM for optimal growth, 200 OK
Antibiotics: If it is appropriate to select for the strain using antibiotics, add 1μl per mL of 1000X stock solution
For best results (but certainly not necessary): Pre-culture for ~6hrs in 20-25% final culture volume Incubate in container with capacity >200% culture volume, overnight

Cryostocking
Any time you generate a new strain (i.e. transform a new combination of DNA parts) you should generate miniprep (for DNA) and a cryostock (for frozen cells).

Procedure
In a cryostock tube (1.8mL tube with screw top), mix a dense liquid culture of the strain with glycerol to the proper percentage (I think there's some flexibility but Jesse usually goes for 20% glycerol for both E. coli and B. subtilis)
(So this might look something like: 500μl liquid culture + 500μl 40% glycerol solution)
Sterile technique is super important when making cryostocks!

Miniprep (Qiagen, modified slightly)
Spin falcon tubes @7600rpm, @4C, for 5min to pellet
Discard supernatant by decanting
Reconstitute pellet in 250μl cold Buffer P1 and transfer to microcentrifuge tube
Add 350μl Buffer P2, invert 4-6 times to mix thoroughly
Let stand for less than 5 minutes
The timing for the next few steps is important. Don’t delay.
Add 350μl Buffer N3, immediately invert 4-6 time to mix thoroughly
This step will form a white precipitate
Immediately spin @max speed for 10min @room temperature
Pipette supernatant into spin column while avoiding the precipitate
Centrifuge 60sec, discard flow-through
Add 750μl Buffer PE to column, let sit for 60sec, spin 60sec
Discard supernatant and spin another 60s to dry
Transfer to clean microfuge tube and let sit 60s
Add 30 or 50μl qH2O and let sit 60s, spin 60s
30 results in higher concentration but lower total yield
Pipette and reapply flow through, sit 60s, spin 60s

Nanodrop
Every time you finish a reaction (and cleanup) you should check to see how much DNA you actually have in your test tube before preceding to the next step. This ensures that reactions that require specific molar ratios (ligations) are run correctly .

Procedure
Make sure you have a pipette that can measure 1μL and an aliquot of your elution buffer
Lift the arm on the nanodrop and load 1 μL of your water/elution buffer aliquot onto the small, silver well (pedestal). Gently close the arm, then reopen the arm and dab the blank liquid off the machine with a kimwipe. Make sure you wipe off the metal nubbin on the arm of the machine, too. Put the arm back down. All this ensures that the nanodrop reading area is clean to begin with
Turn on the computer and open “Nanodrop 2000”
Select “nucleic acid” from the opening menu
A window will pop asking if you want to add this data to the previously saved file. Don’t unless you were the previous user.
The nanodrop will perform a self calibration test for a few seconds
Select the appropriate type of nucleic acid you have in your sample from the dropdown menu. Most likely this is DNA.
Next you need to run a blank. Again load 1μL of your elution buffer onto the pedestal, but this time while the arm is down click the "blank" button on the screen. Wipe down the machine.
Load 1 μL of your sample. Gently close the arm and click the “Read” button
Let it read. If you clicked to create a new file in step 3a, then it will ask you for your filename info and stuff like that. Go through that.
Finally, the results should pop up on the graph and the table below it. Make sure the graph has a good 260/280 ratio (usually greater than 1.75). The graph should have a pronounced peak in the left-center of the plot, and should be pretty low on the right side. The curve of the graph should look relatively smooth.
Generally, the quality of the read should be very high for something like a miniprep and will often be much lower when reading the product of a PCR or digest cleanup
If the graph quality looks pretty good/normal, take note of the "ng/μl" value returned; this is the relevant information giving you the concentration of DNA in your sample
Repeat the scan (literally just click the "Read" button again) 2-3 more times to ensure that the read is consistent, and average the value
Save your data somehow (I just write it down, but you can screen capture if you want) and make sure to write the value on the tube containing the sample, wipe down the nanodrop, gently lower the arm, quit the program, and shut the computer. School’s out, you’re done!

Digestion
20 μL Recipe for any combination of the EcoRI, XbaI, SpeI, PstI:
500-1000 ng DNA (as close to 1 μg as possible)
0.5μL Enzyme 1
0.5μL Enzyme 2
2μl appropriate buffer (see NEB doubledigest finder, but for most biobrick enzymes, CutSmart will work perfectly)
Top up with qH20

Mix reagents, adding enzymes last
Incubate at 37°C for 1-2 hrs (<30 min for HF)
Heat kill at 80°C for 20 minutes if proceeding to ligation

Verification
Gel Casting:
0.75% agarose (if DNA>1000bp)
40mL 1x TAE
0.3 g agarose
1 aliquot (~5μl) gel red

Add dry agarose to clean bottle (small enough to fit in microwave)
Add 40mL 1x TAE buffer
Microwave with cap on but loose, swish periodically, until solution is clear and smooth
Pipette in gel red, directly into solution (heat stable so don’t worry about the temperature)
Pour into gel tray, making sure that tray is oriented and tightly inserted such that leaks will not occur, and that the gel is level

Gel Loading & Running
Lane 1 should be ladder; use 1kb ladder or 100bp ladder depending on the size of your DNA samples
Digests can require more (~1.5x) than the usual amount of loading dye

Gel Imaging (using Typhoon scanner)
Always scan a gel immediately after running
Make sure the scanner area is clean; wipe ONLY with 70% ethanol (or DI) and kimtech wipes
Gel should be placed on scanner face-up. That is, the wells should be oriented up, the same way the gel is oriented in the gel box

Gel Extraction & Cleanup
Make sure to place gel on transilluminator face down (wells toward the glass)
Remove as much excess gel matrix as possible without overexposing DNA to UV

For cleanup, follow protocol for using the Wizard PCR Cleanup Kit, found below in PCR section

Ligation (adapted from openwetware ligation protocol):
10 μl Recipe:
30-50 ng vector DNA (A calculator to make life easy)
1μl (10%) 10X T4 DNA ligase buffer
0.5μl (.5%) T4 DNA ligase
Top up w/ qH20 up to 10uL

Procedure
Usually heat inactivation of digests is sufficient; difficult ligations might require a proper cleanup
As often as possible, use isolated inserts and vectors to avoid unwanted ligations
If the reaction needs to be greater than 10μl, adjust amount of 10X ligase buffer and T4 DNA ligase so that they remain at 1% and .5% by volume, respectively
For cohesive (sticky) ends, incubate at 16°C overnight or room temperature for 10 minutes.
For blunt ends or single base overhangs, incubate at 16°C overnight or room temperature for 2 hours (alternatively, high concentration T4 DNA Ligase can be used in a 10 minute ligation).

Chemically Competent Transformation
Materials:
1 aliquot of competent cells
2-4μl ligation mixture
500μl SOC media

Procedure
Thaw cells at 4°C for 5 minutes
Gently mix in ligation product
Incubate at 4°C for 20 min
Meanwhile, warm SOC media to 37°C
Heat shock at 42°C for 30 sec (45 sec for NEB5-alpha cells)
Return to 4°C for 1 min
Add 500μl pre-heated SOC
Incubate at 37°C for 1hr with shaking
Meanwhile, pre-heat plates to 37°C
Plate, one plate w/ 100μl, one plate w/ 150μl

Acetobacter Transformation (electroporation)


PAGE Gel Preparation, Running, and Scanning (proteins only)
Setting up and Running the Gel 1. Use NuPAGE (NOT Bolt) gels, located in middle room fridge on top shelf, far left 2. Keep the gel in its case and rinse off with DW water 3. Carefully remove comb from the case by pulling out from both sides, be gentle! Also remove white tape on bottom for current circulation when gel is running 4. Keep gel in its case. Load gel into running box (upright). Make sure gel is secure and the segment for loading the wells is on the side opposite you. 5. Add SDS running buffer (not MOPS!) so wells overflow into front of the box 6. Before loading must wash out each gel well by pipetting gently up and down 7. Prepare loading samples (also refer to gel kit instructions) a) 7.5ul of product + 2.5ul SeeBlue loading dye in each well b) 6ul SeeBlue NuPAGE ladder (purple top, keep refrigerated) 8. BEFORE LOADING SAMPLES HEAT THEM for 10 minutes at 70 C 9. Load gel with ladder and dyed samples NOTE: When you load a PAGE gel push pipette against the front of the box. The gel has 12 wells, if you do not need to use all 12, then avoid using the very first and the very last well; as the gel runs the current pulls unevenly from the sides (creates “smiling effect” that can make interpreting the scan more difficult) 10. Run gel for 35 minutes at 150-200V

Fixing and Staining the Gel 1. After running, the gel needs to be fixed, stained overnight, and then washed before it can be scanned on the Typhoon scanner. Prepare fixing solution for the gel (ideally you should do this while the gel is running) Fix solution recipe: 50% methanol, 7% acetic acid, fill with milliQ water to 200ul 2. Remove the gel from the running case and place it in a clean container with fixing solution 3. Put gel in 100ul of fix solution and shake in RT at 80rpm for 30 minutes 4. Repeat step 3 with remaining 100ul fix solution 5. Remove all fix solution from container with the gel 6. Soak gel in 60ml SYPRO Ruby gel stain, shake overnight at 80rpm in RT.

Washing and Scanning the Gel 1. Remove PAGE gel from overnight staining and put into new, clean container 2. Wash gel in 100ul of wash solution for 30 minutes in 70-80rpm for 30 minutes Wash solution recipe: 10% methanol, 7% acetic acid, fill with milliQ water until 100ul 3. Remove gel from wash and rinse twice with DI water for 5 minutes to remove all wash to prevent damage to scanner

Scanning a Protein PAGE gel 1. Same as DNA gel, specify size of the gel for the scanner. When loading, make sure to be gentle with the gel (it’s fragile!) and carefully separate combs when on the scanner so you can tell which well is which

PCR (Polymerase Chain Reaction)
Templates 1. Amplifying from a plasmid or isolated sample of DNA You have a tube of linear or plasmid DNA like that from the registry directly and don’t want to wait for the the transformation and miniprep. (note: you should go through the time-intensive transformation in parallel regardless).

In this case, you need first to know the concentration of your sample. If you don’t know it or it was not provided, you can learn the concentration for your sample by using the nanodrop machine located in room 347. It depends on the size of your template, but as a general rule, you need on the order of 25-50 ng template minimum for a successful PCR, so adjust the volume of your template in your PCR accordingly.

2. Colony PCR You can also amplify plasmid or genomic DNA straight from live cultures of organisms containing your desired sequence. You will usually have cultures in one of two forms: either in liquid culture, or spread on an agar plate. If you are amplifying from liquid culture, grow it up as much as you can and add 1μL of the culture to the PCR mix. If you're amplifying from the plate, there is no need to add a volume; instead, simply take a pipette with a pipette tip from the green box, gently touch the pipette tip to the desired colony on the plate (try to take as little from the plate as possible; agar can screw up PCRs), and then insert your pipette tip into the PCR mixture and pipette up and down to mix.

Polymerases and Master Mixes GoTaq Green http://www.promega.com/resources/protocols/product-information-sheets/g/gotaq-green-master-mix-m712-protocol/ Q5 Polymerase Q5 is a fast, high-fidelity polymerase that even beats Phusion. Unlike Taq, Q5 produces blunt-end amplicons. It’s also very expensive so treat it carefully. 25 μL recipe: 5 μL 5x Q5 buffer 0.5 μL 10mM dNTPS 1.25 μL forward primer (10μM dilution) 1.25 μL reverse primer (10μM dilution) Template DNA (a couple nanograms worth) qH2O to 24.75 μL 0.25 μL Q5 enzyme (add last)

The 50uL recipe (when you needs lots of product) is simply double.

Thermocycler Conditions Taq polymerase (GoTaq Green) Initial Denature: 95°C 2 min The official Platinum Blue protocol calls for 94°C for 3 min, although I have never done it that way. Either will work, I am sure. Denature: 94°C 15-30 secs Use a shorter time if the amplicon is a relatively short segment of DNA, and a longer time if it is a relatively long piece of DNA. Annealing X°C 15-30 secs

This is the most crucial step of the thermocycle! Your annealing temperature will be determined by the melting temperature of your primers. As a general rule, your annealing temperature should be about 5° lower than the lowest melting temperature of your primer pair. Additionally, if you are trying to add tails to you amplicon (e.g. you are trying to add restriction sites to the ends of your DNA template), you may need to drop the annealing temperature down even more. I have had primers with melting temperatures above 65° that needed to be annealed at 42°. Additionally, if a primer may be difficult to anneal to the template, you can increase the annealing time for better results. Extension 72° X seconds Taq extension runs at 1kb per minute. Therefore, allow the extension step enough time to fully copy your entire amplicon. Repeat steps 2-4 32X Final Extension 72°C 5 min Hold 4°C forever Q5 Initial Denature at 98°C for 30 sec Denature at 98°C for 10 sec

3. Annealing at X°C for 15-30 sec Use the NEB calculator: https://www.neb.com/tools-and-resources/interactive-tools/tm-calculator Extension at 72°C for X seconds Q5 is much faster than Taq, and requires 20-30 sec per kb. Go to step two 25-35X Final extension at 72°C for 2 min Hold 10°C forever (zero minutes=forever)

The standard protocols for various polymerases can be found at these addresses:
GoTaq: http://www.promega.com/resources/protocols/product-information-sheets/g/gotaq-green-master-mix-m712-protocol/
Q5: https://www.neb.com/protocols/2012/09/27/pcr-using-q5-high-fidelity-dna-polymerase-m0491

PCR Cleanup (using Wizard SV Gel and PCR Purification System)
Sample Prep

Gel Extraction: Following electrophoresis, excise DNA band from gel and place gel slice in a 1.5ml microcentrifuge tube. Trim the slice of parts that don’t contain DNA Weigh gel slice (by weighing the tube containing the slice and subtracting the mass of the empty tube) Add 10μl Membrane Binding Solution per 10 mg of gel slice. Vortex and incubate at 50–65°C until gel slice is completely dissolved (usually 10-15 minutes)

PCR Amplifications: Add an equal volume of Membrane Binding Solution to the PCR amplification.
Binding of DNA
Insert SV Minicolumn into Collection Tube.
Transfer dissolved gel mixture or prepared PCR product to the Minicolumn assembly. Incubate at room temperature for 1 minute.
Centrifuge at max speed for 1 minute. Discard flowthrough and reinsert Minicolumn into Collection Tube. If you are worried about the final concentration of your purified product, you can repeat this step to maximize the amount of DNA bound to the filter. Washing
Add 700μl Membrane Wash Solution (ethanol added). Centrifuge at max speed for 1 minute. Discard flowthrough and reinsert Minicolumn into Collection Tube. Repeat Step 4 with 500μl Membrane Wash Solution. Centrifuge at max speed for 5 minutes. Empty the Collection Tube and re-centrifuge the column assembly for 1 minute with the microcentrifuge lid open (or off) to allow evaporation of any residual ethanol.

Elution Carefully transfer Minicolumn to a clean 1.5ml microcentrifuge tube. Add 30-50 μL of Nuclease-Free Water to the center of the minicolumn. Incubate at room temperature for 1 minute. Centrifuge at max speed for 1 minute. By adding less water, like 30 μl, you will increase the concentration but decrease the total amount of product. On the flipside, if you want to maximize product, you can maximize elution volume so long as you don’t care about concentration.
Note: you can also increase yield by warming the elution water before hand. I usually warm it to 40°C with good results.
Discard Minicolumn and take sample to nanodrop (see 'Nanodrop', below) Store DNA at –20°C.

The standard protocols for the SV Wizard Gel and PCR purification kit can be found here: http://www.promega.com/resources/protocols/technical-bulletins/ 101/wizard-sv-gel-and-pcr-cleanup-system-protocol/

ELIM Biopharm: Primers & Sequencing

Primers

Designing Primers
Choose a forward and reverse primer from a location in the gene or plasmid that is sure to include the portion desired for amplification or sequencing For sequencing, it is desirable if possible to have primers that fall 50-150bp outside your desired region, to ensure that accurate reading occurs for the whole gene (often the first and last ~100bp in the read are very inaccurate) For PCR remember that the sequence portion corresponding to the primers themselves will be amplified also Primers should normally be between 15-30bp in length (around 20bp is ideal)
Desired melting temperatures are generally between 55-65°C As you will see, melting temperature is a function of length and GC content, so it is often difficult to design primers in regions much greater than 50% AT Forward and reverse primers should have the same melting temperature, or with a difference of no more than 3 degrees The annealing temperature used for a pair of primers should be set at 5 degrees below the lower melting point of the primer pair Using a tool like ApE or Geneious makes it easy to select certain sections of a sequence to check for primer features like melting point and GC content IDTs 'Oligo Analyzer' is a great tool to check for primer dimerization, hairpin structures, etc. http://www.idtdna.com/analyzer/Applications/OligoAnalyzer/ Use this tool or something like it as a final check to make sure your primers will not be likely to react with themselves or each other around the temperatures they will be active for gene interaction NCBI Primer Blast is another great tool. It can be used both to help design the primers and to ensure that the primers you choose will not amplify any genomic DNA in a colony based amplification http://www.ncbi.nlm.nih.gov/tools/primer-blast/ Primer Blast isn’t perfect. It will often miss off-target products, or predict ones that don’t happen. Special BioBrick considerations

Ordering Primers We order our primers from ELIM Biopharm (http://elimbio.com/) The rest is fairly self-explanatory, but we'll do a walk through when you get here Primers <36bp ordered before 5pm will arrive the next day Delivery is around 2:15pm

Primer Dilution (stock preparation) Once you receive your primers, you need to dilute them; Kosuke does 1/10 dilutions, iGEM typically uses 1/20 (10μM) dilutions Typically we create 100-200μl working stocks; it will take a long time to use up that much primer
Example: 10μL primer stock 190μL qH2O or TE buffer Sequencing Two main reasons: After a difficult pcr/gel extraction to ensure the product is correct After cloning/biobricking to ensure no errors were introduced during PCR

Ordering Sequencing You can put in the order using the same general procedure for ordering primers The important difference is either before or right after ordering, you need to actually prepare the DNA that will be picked up for sequencing (see Premix Specifications below) For DNA pickups for sequencing, the guy usually shows up around 2PM, so if you want an order picked up day of, be sure to have everything put together by lunchtime This can usually be done even if you're miniprepping the sample that morning; preparing the sample for sequencing doesn't take too long unless you have a lot of samples to prepare He always picks up the samples from room 3 , there's a file box labeled "ELIM" Print out the order confirmation sheet and staple a baggy with your samples to it and put it in the box Premix Specifications (plasmid DNA) Prepare the DNA as specified by ELIM. For plasmids, this looks like: 500ng DNA 0.8μl primer (one primer per sequencing reaction) Top up w/ qH20 to 15μL For sequencing other DNA (e.g. PCR product) see the ELIM website for specifications: http://www.elimbio.com/Sample_Preparation.htm

Checking the Data Usually sequencing data will be available the morning after you put in the order, sometimes early, sometimes closer to lunchtime
The results can be accessed again through the ELIM site; after signing in, there is an option to "retrieve/download sequencing data" You can either just view, or download the files I recommend downloading all the files because you'll want to view them all anyway Tools like ApE or Geneious will be needed to properly read the files Each sequence read will come with a '.ab1' file that visualizes the data, and a '.seq' file that actually gives you the sequence they read Check the ab1 file first; you're hoping for strong clear peaks, where one of four different colors represents each possible base Typically the beginning and end of the read will look sloppy, but the middle few hundred bases should look very pretty If the read looks pretty clean, then open the .seq file and compare the sequence to the theoretical sequence

Gene Synthesis

iGEM and the Registry of Standard Biological Parts
Using iGEM Registry DNA
Detailed instructions for locating a particular part and reconstituting that DNA from the iGEM distribution plates can be found here: http://partsregistry.org/Help:Distribution_Kits The plates are currently stored in the freezer in room 378

Important points:
Transform the DNA into an E. coli cloning strain e.g. DH5α As always when generating a new strain: grow a liquid culture, cryostock the strain, and miniprep to have a source of the DNA

Creating a Registry Page for a New Part
The iGEM site guides you through this pretty well. From the main page for the Registry you will see a link for 'add a part' and go from there You will have options for submitting basic parts or composite parts; usually whatever functional unit you end up using in the iGEM projects will be a composite part, but for every composite part you'll also want to create an individual part page for the basic parts from which it is made In fact, the basic parts pages should be made first, so you can reference them in creating the page for the composite part

Cultures

Bacillus subtilis

Bacillus subtilis Transformation
Phase 1
1.inoculate 25% (5mL) of desired final volume of LB with BS168 in the morning, in container >200% final volume (50mL falcon tube) 2.incubate @37C for ~6hrs, then top up to final volume (20mL) LB to incubate overnight 3.spin and pellet @3000g for 5 min 4.wash with cold (4C) sterile deionized water by resuspending (in 25-50% original volume) and spinning @3000g for 5min 5.discard supernatant, repeat twice more 6.finally resuspend in 1% of the original culture volume (from which the pellet was formed) with cold (4C) 30% PEG solution 7.aliquot into 100μl samples (use pre-chilled tubes) 8.freeze immediately @ -80C 9.after waiting overnight, proceed to phase 2

Phase 2 (electroporation)
1.thaw cells @ 4C until liquid 2.transfer to cold .2cm electroporation cuvette 3.apply current with cuvette uncapped, @ 25μF, 2.5kV (12.5kV/cm), 400ohms 4.immediately add 2ml of prewarmed SOC to cuvette, cap, and mix by inverting several times 5.transfer cuvette contents to 15ml falcon tube by pipetting or decanting and incubate for 90 min @37C 6.plate on preheated selective agar (if unsure about efficiency, try 100μl, 15μl) Escherichia coli (adapted from Dr. Shih’s protocol) Doubling time for E.coli in ideal conditions, 37ºC = 20 minutes

Site Directed Mutagenesis

1. How to make primers (http://openwetware.org/wiki/Richard_Lab:Site_Directed_Mutagenesis)
Double primer method:
Design mutagenesis primers. The targeted mutation should be included into both primers. The mutation can be as close as 4 bases from the 5-terminus. The mutation should be at least 8 bases from the 3-terminus. At least eight non-overlapping bases should be introduced at the 3-end of each primer. At least one G or C should be at the end of each primer. Design your primers (including the mutations) to have a Tm >=78°C.

Single primer method: Design mutagenesis primer(s). The targeted mutation should be in the middle of the primer Design your primers (including the mutations) to have a Tm >=78°C.

2. How to use thermal cycling: Specifics can be found in the QuikChange Lightning Site-Directed Mutagenesis Kit http://www.chem.agilent.com/library/usermanuals/Public/210518.pdf http://www.biomedcentral.com/1472-6750/8/91