Team:CIDEB-UANL Mexico/Test/Protocol

From 2012hs.igem.org

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<h2>Minipreps of plasmidic DNA</h2>
<h2>Minipreps of plasmidic DNA</h2>
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<p>1.Add 1.5 mL of culture inside an Eppendorf tube. Centrifuge at 14000 rpm for 30 seconds and throw the supernatant away inside a container with chlorine at 0.1% or with liquid soap.
+
<p><li>1.Add 1.5 mL of culture inside an Eppendorf tube. Centrifuge at 14000 rpm for 30 seconds and throw the supernatant away inside a container with chlorine at 0.1% or with liquid soap.</li>
-
2.Add 200 μL of Solution I and mix giving vortex until the pill is completely dissolved. (A micropipette can be used if it’s difficult to dissolve).
+
<li>2.Add 200 μL of Solution I and mix giving vortex until the pill is completely dissolved. (A micropipette can be used if it’s difficult to dissolve).</li>
-
3.Leave all at room temperature from 5 to 10 minutes.
+
<li>3.Leave all at room temperature from 5 to 10 minutes.</li>
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4.Add 200 μL of Solution II and mix by inversion. Leave at room temperature from 5 to 10 minutes.
+
<li>4.Add 200 μL of Solution II and mix by inversion. Leave at room temperature from 5 to 10 minutes.</li>
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5.Add 200 μL of Solution III and mix by inversion. Leave all the samples in ice for about 10 minutes.
+
<li>5.Add 200 μL of Solution III and mix by inversion. Leave all the samples in ice for about 10 minutes.</li>
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6.Centrifuge at 14,000 rmp for 5 minutes.
+
<li>6.Centrifuge at 14,000 rmp for 5 minutes.</li>
-
7.Pass the supernatant inside a new Eppendorf tube containing 1mL of ethanol at 100% by using a tip, being careful of not passing any precipitate.  
+
<li>7.Pass the supernatant inside a new Eppendorf tube containing 1mL of ethanol at 100% by using a tip, being careful of not passing any precipitate.</li>
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8.Incubate at 20°C for 10 minutes (From 10 minutes to 2 hours).
+
<li>8.Incubate at 20°C for 10 minutes (From 10 minutes to 2 hours).</li>
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9.Centrifuge at 14,000 rpm for 10 minutes and throw the supernatant away.
+
<li>9.Centrifuge at 14,000 rpm for 10 minutes and throw the supernatant away.</li>
-
10.Add 200 μL of etanol at 70% and give vortex for a few seconds.
+
<li>10.Add 200 μL of etanol at 70% and give vortex for a few seconds.</li>
-
11.Centrifuge at 14,000 rpm for 5 minutes and remove the sobrenatant using a tip.
+
<li>11.Centrifuge at 14,000 rpm for 5 minutes and remove the sobrenatant using a tip.</li>
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12.Dry the pill at 37°C for 5 minutes in the incubator.
+
<li>12.Dry the pill at 37°C for 5 minutes in the incubator.</li>
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13.Add 20 μL of mQ water with RNAse (10ng/ μL) and resuspend with wortex.  
+
<li>13.Add 20 μL of mQ water with RNAse (10ng/ μL) and resuspend with wortex.</li>
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14.Run a gel or store at 4°C  (DNA Electroforesis in agarose gel)</p>
+
<li>14.Run a gel or store at 4°C  (DNA Electroforesis in agarose gel).</li></p>
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<h2>Quantification of DNA by Ultra Violet Spectrophotometry</h2>  
<h2>Quantification of DNA by Ultra Violet Spectrophotometry</h2>  
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<p>1.Take 1ml of mQ water and place it inside a 1.5mL Eppendorf tube.
+
<p><li>1.Take 1ml of mQ water and place it inside a 1.5mL Eppendorf tube.</li>
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2.Add 1 μL of plasmidic DNA samples of E.coli. (Dilution 1:1,000).
+
<li>2.Add 1 μL of plasmidic DNA samples of E.coli. (Dilution 1:1,000).</li>
-
3.Calibrate the spectrophotometer with a cell containing 1mL of distillated water.
+
<li>3.Calibrate the spectrophotometer with a cell containing 1mL of distillated water.</li>
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4.Pass the sample of the Eppendorf tube to a cell of the spectrophotometer by using a micropipette.
+
<li>4.Pass the sample of the Eppendorf tube to a cell of the spectrophotometer by using a micropipette.</li>
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5.Place the cell in the spectrophotometer.
+
<li>5.Place the cell in the spectrophotometer.</li>
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6.Select the DNA or RNA option in the machine.
+
<li>6.Select the DNA or RNA option in the machine.</li>
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7.Select the DNA option in the spectrophotometer.
+
<li>7.Select the DNA option in the spectrophotometer.<li>
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8.Read the absorbance of the sample with the spectrophotometer.
+
<li>8.Read the absorbance of the sample with the spectrophotometer.</li>
-
9.Annotate the reading made at 260, 280 and 320 nm, the relation 260/280 and the concentration given by the spectrophotometer.
+
<li>9.Annotate the reading made at 260, 280 and 320 nm, the relation 260/280 and the concentration given by the spectrophotometer.</li>
-
10.Remove the cell from the spectrophotometer and throw away its containing into a biological wastes container.
+
<li>10.Remove the cell from the spectrophotometer and throw away its containing into a biological wastes container.</li>
-
11.Wash the cell, first with distillated water and then with ethanol at 100% and put it in a chemical wastes container.
+
<li>11.Wash the cell, first with distillated water and then with ethanol at 100% and put it in a chemical wastes container.</li>
-
12.Let the cell dry so it can be reused. (It’s recommended to use the same used solution).</p>
+
<li>12.Let the cell dry so it can be reused. (It’s recommended to use the same used solution).</li></p>
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<h2>Plasmidic DNA characterization</h2>
<h2>Plasmidic DNA characterization</h2>
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<p>1.Prepare the mix.
+
<p><li>1.Prepare the mix.</li>
-
2.Distribute  the mix in equal parts.
+
<li>2.Distribute  the mix in equal parts.</li>
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3.Add the sample of DNA to the reactions and give a soft vortex.
+
<li>3.Add the sample of DNA to the reactions and give a soft vortex.</li>
-
4.Incubate the reactions at 37°C in the incubator from 1 to 12 hours.
+
<li>4.Incubate the reactions at 37°C in the incubator from 1 to 12 hours.
5.Run the agarose to check the result.</p>
5.Run the agarose to check the result.</p>
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<h2>BioBrick Pieces Assembly</h2>
<h2>BioBrick Pieces Assembly</h2>
-
<p>1.Prepare the mix. (Reaction order: mQ water > Buffer > Enzyme).
+
<p><li>1.Prepare the mix. (Reaction order: mQ water > Buffer > Enzyme).</li>
-
2.Distribute the mix in equal parts.
+
<li>2.Distribute the mix in equal parts.</li>
-
3.Add the sample of DNA to the reactions and give a soft vortex.
+
<li>3.Add the sample of DNA to the reactions and give a soft vortex.</li>
-
4.Incubate the reactions at 37°C in the incubator from 1 to 12 hours.
+
<li>4.Incubate the reactions at 37°C in the incubator from 1 to 12 hours.</li>
-
5.Run 10 μL in agarose gel.
+
<li>5.Run 10 μL in agarose gel.</li>
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6.Store 10 μL for its posterior ligation.</p>
+
<li>6.Store 10 μL for its posterior ligation.</li></p>
<h2>Genetic parts ligation</h2>
<h2>Genetic parts ligation</h2>
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<p>1.Take in account the concentration of every sample that now contain the fragments which will used bind.
+
<p><li>1.Take in account the concentration of every sample that now contain the fragments which will used bind.</li>
-
2.Use the Ligation Calculator to obtain the quantities to separate the ligation MIX  with a final volume of 20 μL.!
+
<li>2.Use the Ligation Calculator to obtain the quantities to separate the ligation MIX  with a final volume of 20 μL.!</li>
-
3.Prepare the mix using the quantities given by the calculator in the following order: Agua mQ >Ligation Buffer>Vector/Fragment.
+
<li>3.Prepare the mix using the quantities given by the calculator in the following order: Agua mQ >Ligation Buffer>Vector/Fragment.</li>
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4.Distribute the ligation mix if necessary and add the ligase T4.
+
<li>4.Distribute the ligation mix if necessary and add the ligase T4.</li>
-
5.Incubate the reactions at 25°C (room temperature) for an 1 hour or all night long.</p>
+
<li<5.Incubate the reactions at 25°C (room temperature) for an 1 hour or all night long.</li></p>
       </div>
       </div>

Revision as of 18:34, 16 June 2012

Web Site for Igem project of CIDEB

Lab Protocols

Use of plates with BioBrick lyophilazed

  • 1.Search in the Part Registry web site for the desired BioBrick and locate its exact ubication in the DNAs’ plate.
  • 2.Position correctly the lyophilizated DNAs’ plate.
  • 3.Using a 10 μl micropipette, take a white tip and drill the aluminum cover in the well where is located the BioBrick piece.
  • 4.Using the same micropipette, throw away the tip, take another one to take 10 μl of mQ water and introduce this tip in the well.
  • 5.Up and down the liquid using the micropipette a couple of times until the DNA is completely resuspended (when dissolving the DNA, it will give to the water a reddish coloration, so, the more reddish the solution, the better the suspension).
  • 6.Pour the liquid in a 0.6 μl Eppendorf tube, label and store.

    • Preparation of competent cells of E.coli and their transformation

  • Preparation of Ca+ Competent Cells
  • 1.Inoculate a DH5T cells colony in 5ml of Luria Bertani medium (LB) without antibiotic. Incubate all night long at 37 Celsius degrees with constantly agitation.
  • 2.Inoculate 1/100 of the volume of these cells to 100ml of LB medium, incubate at 37 Celsius degrees with constantly agitation until reach a DO6000.34!(~5x108!cel/mL).
  • 3.Cool the culture in ice for 5 minutes.
  • 4.Centrifuge for 8 minutes at 1700 × g 4° C.
  • 5.Resuspend gently the pill in 20mL of 0.1 M calcium chloride cooled in ice.
  • 6.Centrifuge for 8 minutes at 1700 × g 4° C.
  • 7.Resuspend the pill in 4ml of 0.1 M calcium chloride cooled in ice.
  • 8.Store in ice for a week until its use.

  • Transformation of Ca+ Competent cells
  • 1.In a 1.5mL Eppendorf tube pre-cooled, add 50 μl of competent bacteria. (It’s very important to keep the materials at 4°C).
  • 2.Add 2 μl of DNA and mix giving some light hits among the tubes.
  • 3.Stand in ice from 20 to 30 minutes.
  • 4.Give the thermal shock by immersing the Eppendorf tubes inside a beaker with water at 42°C for a minute. 5.Put the tubes back in the ice for 2 minutes.
  • 6.Add 200 μl of LB medium and incubate at 37°C from 20 to 30 minutes.
  • 7.Culture in LB boxes with their respective antibiotic and incubate at 37°C all night long.

    • Inoculation in petri dish and in test tube

  • Stria in plate
  • 1.Take the bacteriological handle and introduce in the flame of the burner until the point of the handle gets red, so it can be sterilized.
  • 2.Take it away from the flame and wait until it’s a little bit cooled.
  • 3.Introduce the sterilized handle inside the tube that contains the bacteria and take a drop of the culture.
  • 4.Take it away from the tube and inoculate the plate by stria forming parallel lines, spreading it over the agar. 5.First, inoculating a corner, sterilize the handle again and spread from a corner the bacteria previously inoculate, sterilize again and finish with wide movements.
  • 6.Incubate the plate at 37°C from 18 to 24 hours.

    • Extension on surface (When cultivating a transformation)

  • 1.Take the inoculum using a micropipette and place it in the agar surface.
  • 2.Take the glass bar and introduce it in a beaker with alcohcol.
  • 3.Put it away and quickly pass it by the flame and cool it a little bit.
  • 4.Place the bar in the agar without making any contact with the dumped culture.
  • 5.Spread the inoculum in the plate until it’s dry.
  • 6.Incubate the plate at 37°C from 18 to 24 hours.

    • Inoculation in test tube from plate (Peck colonies for cloning)

  • 1.Add the correct antibiotic to a test tube with culture medium.
  • 2.Peck a colony with a bacteriologic handle previously sterilized o peck with the point of the micropipette.
  • 3.Shake by making small circles in the culture (if a handle was used) or up and down the culture a couple of times (if a micropipette was used).
  • 4.Incubate at 37°C with vigorous and continuous agitation from 16 to 18 hours.

    • Reculture bacteria from test tube to test tube

  • 1.Add the correct antibiotic to a test tube containing culture medium.
  • 2.Take approx. 20 μL of cultura containing bacteria and introduce them into a test tube with the new culture medium.
  • 3.Incubate at 37°C with vigorous and continuous agitation from 16 to 18 hours.

    • Minipreps of plasmidic DNA

  • 1.Add 1.5 mL of culture inside an Eppendorf tube. Centrifuge at 14000 rpm for 30 seconds and throw the supernatant away inside a container with chlorine at 0.1% or with liquid soap.
  • 2.Add 200 μL of Solution I and mix giving vortex until the pill is completely dissolved. (A micropipette can be used if it’s difficult to dissolve).
  • 3.Leave all at room temperature from 5 to 10 minutes.
  • 4.Add 200 μL of Solution II and mix by inversion. Leave at room temperature from 5 to 10 minutes.
  • 5.Add 200 μL of Solution III and mix by inversion. Leave all the samples in ice for about 10 minutes.
  • 6.Centrifuge at 14,000 rmp for 5 minutes.
  • 7.Pass the supernatant inside a new Eppendorf tube containing 1mL of ethanol at 100% by using a tip, being careful of not passing any precipitate.
  • 8.Incubate at 20°C for 10 minutes (From 10 minutes to 2 hours).
  • 9.Centrifuge at 14,000 rpm for 10 minutes and throw the supernatant away.
  • 10.Add 200 μL of etanol at 70% and give vortex for a few seconds.
  • 11.Centrifuge at 14,000 rpm for 5 minutes and remove the sobrenatant using a tip.
  • 12.Dry the pill at 37°C for 5 minutes in the incubator.
  • 13.Add 20 μL of mQ water with RNAse (10ng/ μL) and resuspend with wortex.
  • 14.Run a gel or store at 4°C (DNA Electroforesis in agarose gel).

    • Quantification of DNA by Ultra Violet Spectrophotometry

  • 1.Take 1ml of mQ water and place it inside a 1.5mL Eppendorf tube.
  • 2.Add 1 μL of plasmidic DNA samples of E.coli. (Dilution 1:1,000).
  • 3.Calibrate the spectrophotometer with a cell containing 1mL of distillated water.
  • 4.Pass the sample of the Eppendorf tube to a cell of the spectrophotometer by using a micropipette.
  • 5.Place the cell in the spectrophotometer.
  • 6.Select the DNA or RNA option in the machine.
  • 7.Select the DNA option in the spectrophotometer.
  • 8.Read the absorbance of the sample with the spectrophotometer.
  • 9.Annotate the reading made at 260, 280 and 320 nm, the relation 260/280 and the concentration given by the spectrophotometer.
  • 10.Remove the cell from the spectrophotometer and throw away its containing into a biological wastes container.
  • 11.Wash the cell, first with distillated water and then with ethanol at 100% and put it in a chemical wastes container.
  • 12.Let the cell dry so it can be reused. (It’s recommended to use the same used solution).

    • Plasmidic DNA characterization

  • 1.Prepare the mix.
  • 2.Distribute the mix in equal parts.
  • 3.Add the sample of DNA to the reactions and give a soft vortex.
  • 4.Incubate the reactions at 37°C in the incubator from 1 to 12 hours. 5.Run the agarose to check the result.

    BioBrick Pieces Assembly

  • 1.Prepare the mix. (Reaction order: mQ water > Buffer > Enzyme).
  • 2.Distribute the mix in equal parts.
  • 3.Add the sample of DNA to the reactions and give a soft vortex.
  • 4.Incubate the reactions at 37°C in the incubator from 1 to 12 hours.
  • 5.Run 10 μL in agarose gel.
  • 6.Store 10 μL for its posterior ligation.

    • Genetic parts ligation

  • 1.Take in account the concentration of every sample that now contain the fragments which will used bind.
  • 2.Use the Ligation Calculator to obtain the quantities to separate the ligation MIX with a final volume of 20 μL.!
  • 3.Prepare the mix using the quantities given by the calculator in the following order: Agua mQ >Ligation Buffer>Vector/Fragment.
  • 4.Distribute the ligation mix if necessary and add the ligase T4.

    • iGEM High School Division, 2012 edition - CIDEB-UANL_Mexico team

    Retrieved from "http://2012hs.igem.org/Team:CIDEB-UANL_Mexico/Test/Protocol"