Another way is one use throwable plastic hoop. Which is completely stupid, but well…
Comment on Prove your humanity.
Sterile_Technique@lemmy.world 1 day agoPretty much. It’s like a little wire loop - sterilize it with a bunsen burner, let it cool, then take a swab from your source specimen and drag it into your agar for that section 1. Sterilize it again with the burner, cool, then drag through the last couple lines of 1 to get region 2. Repeat for 3 and again for 4. The sample size of individual microbes gets exponentially fewer each time - done correctly and region 4 is dotted with individual cells, which you leave alone for a while to incubate, then come back and start making your observations like how it’s interacting with the agar, what color, texture etc; smear it onto a microscope slide, see how it responds to different stains, it’s shape, it’s arrangement… then start checking all those findings against known properties of different microbes until you find a match.
BrowseMan@sh.itjust.works 8 hours ago
janus2@lemmy.zip 10 hours ago
raise your hand if you ever wrecked a plate by forgetting to cool the loop
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Sterile_Technique@lemmy.world 10 hours ago
I made that mistake several times, but iirc it was always a recoverable error. When I stuck that hot loop into the agar it would sizzle, which would tell me I just murdered every bacterium that loop touched; so resterilize actually allow it to cool this time, and repeat the botched step in a slightly different location to pass through a section of bacteria that I hadn’t just dropped a nuke on.
…which is probably shitty technique, but it got me good enough results to get good enough data for class.
janus2@lemmy.zip 10 hours ago
This would have been a handy technique if in addition to forgetting to cool the loop I also noticed that I had forgot to cool the loop lol