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Hello students.
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Today we are solving a question in biology.
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As you can see from a question day, given us that, cinearhabitis elegance is undergoing p.
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Arogenosa assay, which is a liquid killing assay, and it was performed on cine or haptitis elegance, which is nothing but a transparent nematose.
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Cine or haptiditis elegance is a transparent nematose.
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A liquid killing assay was performed essentially described on anderson.
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In brief, the worms were synchronized by bleaching, gravid uddles and hatching in the absence of foot at 15 degrees celsius.
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The larvae were dropped onto plates containing standard e.
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Coli and then transferred non -permissive temperature to induce stability.
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Okay, so basically an experiment was performed with cinerhabitis elegance where the larvae is poured into a medium of e.
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Coli.
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So this is the final picture they've obtained.
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So these are representative images of the cener habditis elegance death after incubation.
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The bacteria was then scrapped and then was inoculated.
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So lk11 demonstrates the dosage dependent was skewed.
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And the cell impermeable dye, cytox orange, was used to stain the dead books.
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So cytox orange was the dye that was used to stain the dye.
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The dead worms and each well in this experiment contains approximately 18 worms.
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Each will contains 18 worms and three biological replicates were performed and dmso is the liquid the drug is dissolved in.
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Now dms is nothing but dimethyl sulfoxyte...