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[Music]
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lb auger plates are commonly used to
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culture individual bacterial colonies
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from freezer stocks or to select
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individual populations from complicated
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bacterial mixtures in this video we'll
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walk you through the steps for making lb
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auger plates we'll show you all the
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materials you'll need for the process
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show you how to sterilize your plates
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indicate best practices during plate
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pouring and will demonstrate how to test
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your plates by the end of this video you
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should be able to prepare LV auger
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plates with your antibiotic of
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interest to begin the plate pouring
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process we'll gather all of our
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necessary materials first we have our lb
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augur powder for every liter of molten
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augur that we make we'll measure out 37
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G of premixed lb AER powder consisting
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of 5 G of peptone 10 G of peptone from
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casin 10 G of sodium chloride and 12 G
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of Ager AER these items can be bought
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premixed or you can buy each separately
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we prefer to buy them premix to save
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time this composition will make 1.2%
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augur plates next we have our sterile
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water our goal is to make 30 gels in 60
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mm x 15 mm plates Each of which can hold
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roughly 5 to 7 Ms of lb augur on plates
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this size you can easily distinguish
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about 100 individual colonies if you're
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going to be doing high volume screening
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we recommend larger plates for the 30
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plates we only need roughly 200 Ms of
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water but just in case we spill a little
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along the way we'll add 220 Ms to start
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because we'll be using these plates for
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selection we'll need antibiotic we keep
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our antibiotics as stock Solutions at
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1000x concentration and dilute them as
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necessary next comes our glass wear and
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disposables we will make the 220 Ms of
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molten lb AER in a 500 mil bottle your
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bottle should always have plenty of
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extra volume so your lb AER doesn't boil
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over in the autoclave we will use the
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sterile pipets to Alo quat the gel mix
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finally we'll use the autoclave tape to
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label our
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bottle now that we have everything ready
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it's time to start making our plates the
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first step is to measure out the elbag
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powder it takes 37 G of powder to make 1
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liter of gel mix since we only need 220
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Ms of gel mix we will measure out 8.14 G
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of elbag powder now we add the elbag
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powder and the sterile water to the
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bottle and swirl to form a colloid do
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not make the seal airtight an airtight
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seal can lead to cracking during the
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sterilization process next we add a
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piece of autoclave tape to the bottle
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autoclave tape darkens when it has been
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at least 10 minutes at 121° C in the
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autoclave and lets us know our lb augur
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has reached the appropriate
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sterilization temperature we also add a
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piece of lab tape to the bottle with our
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initials the date and the bottle
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contents this will clear up any
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confusion should we accidentally leave
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our bottle in the autoclave or if
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somebody opens the autoclave before we
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do autoclaves are used to bring
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materials and media to high temperature
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at high pressure the high temperature
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steril izes our materials while the high
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pressure keeps liquids from boiling over
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some organisms and certain spores can
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however survive in the harsh conditions
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of the autoclave be sure to check the
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literature for the appropriate
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sterilization techniques if you're
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working with any weird and wonderful
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organisms to begin we place our lb aoid
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in the autoclave and seal the door we
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then set the autoclave to reach 121° C
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under 20 psi for 20 minutes and start
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the autoclave cycle do not use the
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autoclave if you have not been prop L
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[Music]
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trained well the elbag sterilizing in
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the autoclave we will prepare our bench
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for plate pouring first we find or make
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an empty section of bench with a working
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flame then we spray down the bench with
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70% ethanol and wipe it with a paper
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towel once the bench is clean we count
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out the appropriate number of plates and
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leave them stacked in an easily
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accessible location be careful not to
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stack them too high lest we have an
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architectural
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disaster now we label our plates with
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the medium and the antibiotic they will
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contain we recommend using a batch
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labeling system to speed up this process
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for instance we simply label our bags
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instead of our plates if you label your
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plates in more detail be sure to write
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on the bottom of the plates instead of
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the
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top next we take our antibiotic out of
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the freezer we keep our antibiotics
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stored as 1000x stock Solutions and
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dilute these as necessary most
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antibiotics can be stored in water but
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some like Chlor fenicol must be stored
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in other solvents like ethanol check
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with the antibiotics manufacturer for
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further
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details we next set a water bath to 60°
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C making sure that the water bath has
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enough water to submerge about 75% of
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our molten lb AER bottle we will cool
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the lb AER mix in the water bath once
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the autoclave cycle is complete 60° C is
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a good temperature because it's warm
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enough for the lb auger to remain in
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liquid form yet cool enough that most
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antibiotics will not
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denat once the autocave cycle is
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complete it's time to retrieve our
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bottle of molten lb augur when handling
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anything coming out of the hot autoclave
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you should always wear thermally
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protective gloves before we retrieve our
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augur it's good practice to leave the
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autoclave door open just a crack for
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about 10 minutes this will allow any
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excess steam to escape and will cool our
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sample slightly after 10 minutes we
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fully open the autoclave remove our
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samples and leave the autoclave door
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open just a crack as a courtesy to the
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next user next we place the bottle with
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the molten lb Aug mix into the 60° C
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water bath submerging about 75% of the
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bottle be careful not to let any of the
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water bath water touch the lip or the
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top of the bottle as this water is not
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likely to be sterile after at least 5
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minutes we remove our molten gel mix
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from the water bath as a good rule of
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thumb if you can hold the bottle with
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lab gloves it's likely cool enough to
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add antibiotic you can use a laser
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thermometer for a more accurate
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temperature
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[Music]
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measurement to begin the plate pouring
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process we light the flame at our gel
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pouring station and dilute our
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antibiotic into the 60° C augur mix
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we're adding 220 microl because we're
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diluting our antibiotic 1 to 1,000 into
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220 mL of augur once the antibiotic is
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added it's time to start pouring our
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plates it's usually faster easier and
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more sterile to pour the molten gel mix
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straight from the bottle however it's
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good practice to measure out the first
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couple of plates using a sterile pipet
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until you get a good feel for the
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appropriate volume don't worry if you
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overfill or spill a little that's why we
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made 220 mL of alagar instead of 200
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you'll get the hang of it and before you
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know it you'll be a plate pouring Pro as
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you pour your plates be careful to recap
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them quickly since that little flame
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certainly won't kill everything that
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could fall on them we stack our plates
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in piles of about five as we pour make
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sure you swirl each plate after you pour
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it if your elb augur partially
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solidifies you should stop pouring and
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remake the gel mix if you're making
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plates without any antibiotic you can
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alternatively reify the lb augur by
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running it through the autoclave again
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or by microwaving if you microwave
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beware of
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overboiling it takes roughly 30 minutes
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for our plates to solidify at room
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temperature however we leave them out
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overnight to allow them to dry
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once dry we place the plates in a
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plastic bag with an absorbent material
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to reduce
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condensation for long-term storage we
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keep our plates in the cold room at 4°
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C even when stored at this temperature
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plates should always be checked for
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contamination prior to use and should
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never be stored for more than a
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month once our plates have solidified
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and dried we test them to make sure the
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antibiotic functions properly to do so
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we pull out two plates on the first
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plate we we streak out a strain that we
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know to be resistant to the antibiotic
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on a second plate we streak out a strain
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that's not resistant to the antibiotic
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we then incubate both plates overnight
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at the appropriate growth temperature if
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we prepared our plates properly only the
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resistance strain should
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grow if only the resistance strain grows
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our plates are ready for use or storage
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at 4°
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C isolating individual colonies on
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plates is a crucial step in many
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experiments because colonies arise from
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single bacteria and are considered
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isogenic thank you for watching our
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plate pouring protocol video if you'd
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like to watch more videos or browse more
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written molecular biology protocols
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