Endy:Pouring plates: Difference between revisions

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This is a general protocol is for the standard preparation of plates.
Also see the [[Endy:Pouring LB plates from prepped media|shortcut method]] for using pre-made 1.2% Agar in LB from the Building 68 media prep room.
==Notes==
==Notes==


*Since 500mL LBAgar makes approxiamtely 20 plates, to make a sufficent quantity to supply the whole lab with plates for a week, you will want to prepare no less than 2L LBAgar at a time.
*(Optional) pre-heat a H2O bath to 55 deg C.  
 
*If you don't know how to use the autoclave, ask for a demo.
*Melt LB ahead of time because it cools to 55 degrees slowly. A good way to do this is melt it in the morning then leave it in the 60 degree incubator or a 60 degree bath. If in a rush, carefully cool by running cold water over the container.


==Materials==
==Materials==
 
For 1 L of Media:
*LB Agar 1.2% (from the media room, very end of the hall on the right)
*10 g of Agar (for 1% Agar plates (w/v))
*Empty plates (above any of the -20 freezers)
*media components specific to media of interest
*antibiotics (liquid stocks from our -20 freezer)
*1 L ddH2O
*Sterile antibiotic stock solution (if required)


==Method==
==Method==
===Preparatation of LB Agar===
===Mixing and Sterilizing Media===
 
#Add dry materials and H2O to a flask sufficiently large to minimize boil-over. (ex.2 L flask for 1 L of media.)
#Obtain 1.2% agar from the media room (500 ml per bottle). SIGN IT OUT - to Endy Lab
#(optional, really unnecessary) add a magnetic stir bar and stir the media.
#Melt in microwave:
#Cover the top of the flask LOOSELY with aluminum foil.
#*use 50% power
#Autoclave the media on the Fluid Cycle, 30 min, 255 deg C. (Keep in mind autoclave reduces pressure slowly. It will take more time than 30 min to execute the cycle.)
#*loosen the cap
#Remove media to 55 deg. H2O bath or room temp to cool.
#*monitor as you melt
#Once media has cooled to ~55 deg. C, add antibiotics, if required.
#*takes approx. 10 minutes per bottle.
#If too hot, let the melted solution cool so that it's warm, but not hot, to the touch - you can use the water bath to do this (50-60 degrees); this won't let it resolidify. At room temp. it may take 20 mins for LB to cool sufficiently.
#ONCE IT'S COOL ENOUGH (50-60 degrees) - add antibiotics: final concentration, 50ug/ml AMP; 20ug/ml KAN. (concentrations of liquid stocks: Amp; 50mg/ml. Kan, 10mg/ml.) (This information posted on the refrigerator with our stuff and antibiotics). For 500mL of LB Agar, use 500uL Amp or 1mL Kan.
#Swirl to mix; try not to make many bubbles.


===Actual Pouring===
===Pouring Plates===


#Obtain a container of empty plates. 1 bottle (500ml) of LB Agar will make about 1 container of plates (20 plates).
#Obtain 2 sleeves of empty plates. 1 L of media will make about 40 plates.
#Using sterile technique, (flame the top of the bottle), pour the LB Agar into the plates. How much to pour? Cover the base of the plate, and then just a bit more after that.
#Using sterile technique, pour the media into the plates.  
#Recap each plate upon pouring. If there are lots of bubbles in your plates (i.e. more than one or two on the edge), you can flame the plate using the small bunsen burner to eliminate bubbles. (See a demo on this).
#*Cover the base of the plate, and then just a bit more after that.
#Leave plates to dry and cool for a while (overnight even). LABEL the stack of plates to indicate antibiotic!
#Recap each plate upon pouring. If there are lots of bubbles in your plates (i.e., more than one or two on the edge), you can flame the plate using the small bunsen burner to eliminate bubbles. (See a demo on this).  Another way to remove the fine bubbles that may be in your flask before puring is to mist the inside of the flask with a 75% ethanol spray bottle.
#Leave plates to dry and cool for a while (overnight even).  
#*It is a good idea to label the stack of plates to indicate antibiotic.
#Store the plates in their original bags - upside down, so that the gel is hanging downwards (this keeps condensation off the gel).
#Store the plates in their original bags - upside down, so that the gel is hanging downwards (this keeps condensation off the gel).
#Label the bags following taping rules:
#Label the bags following taping rules:
#*Red tape in back (indicates LB)
#*Red tape in back (indicates LB)
#*Tape in front indicates antibiotic. (Green: Kan. Yellow: Amp.) (More taping/color rules are on the refrigerator in the second bench room)
#*Tape in front indicates antibiotic (green=Kan, yellow=Amp, more taping/color rules are on the refrigerator in 68-564)
#*also write name of antibiotic, and concentration, on the front piece of tape.
#*Also write name of antibiotic, and concentration, on the front piece of tape.
#Store the labeled bags of plates in the cold room.
#Store the labeled bags of plates in the cold room.


[[Category:Miscellaneous Protocol]]
[[Category:Protocol]]

Latest revision as of 08:38, 14 March 2007

This is a general protocol is for the standard preparation of plates.

Also see the shortcut method for using pre-made 1.2% Agar in LB from the Building 68 media prep room.

Notes

  • (Optional) pre-heat a H2O bath to 55 deg C.
  • If you don't know how to use the autoclave, ask for a demo.

Materials

For 1 L of Media:

  • 10 g of Agar (for 1% Agar plates (w/v))
  • media components specific to media of interest
  • 1 L ddH2O
  • Sterile antibiotic stock solution (if required)

Method

Mixing and Sterilizing Media

  1. Add dry materials and H2O to a flask sufficiently large to minimize boil-over. (ex.2 L flask for 1 L of media.)
  2. (optional, really unnecessary) add a magnetic stir bar and stir the media.
  3. Cover the top of the flask LOOSELY with aluminum foil.
  4. Autoclave the media on the Fluid Cycle, 30 min, 255 deg C. (Keep in mind autoclave reduces pressure slowly. It will take more time than 30 min to execute the cycle.)
  5. Remove media to 55 deg. H2O bath or room temp to cool.
  6. Once media has cooled to ~55 deg. C, add antibiotics, if required.

Pouring Plates

  1. Obtain 2 sleeves of empty plates. 1 L of media will make about 40 plates.
  2. Using sterile technique, pour the media into the plates.
    • Cover the base of the plate, and then just a bit more after that.
  3. Recap each plate upon pouring. If there are lots of bubbles in your plates (i.e., more than one or two on the edge), you can flame the plate using the small bunsen burner to eliminate bubbles. (See a demo on this). Another way to remove the fine bubbles that may be in your flask before puring is to mist the inside of the flask with a 75% ethanol spray bottle.
  4. Leave plates to dry and cool for a while (overnight even).
    • It is a good idea to label the stack of plates to indicate antibiotic.
  5. Store the plates in their original bags - upside down, so that the gel is hanging downwards (this keeps condensation off the gel).
  6. Label the bags following taping rules:
    • Red tape in back (indicates LB)
    • Tape in front indicates antibiotic (green=Kan, yellow=Amp, more taping/color rules are on the refrigerator in 68-564)
    • Also write name of antibiotic, and concentration, on the front piece of tape.
  7. Store the labeled bags of plates in the cold room.
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