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I enjoyed your presentation! Was there any limitations that resulted in the inconclusive results? Or was it just because the Hypzif failed to work? LikeLike Reply
Hi Jesse, thank you! The only limitations were technical errors or malfunctioning materials. LikeLike Reply
Hi Kiley! I would have just ensured that the conditions in which these experiments were run were more ideal and that all of the reagents were uncontaminated and functional. LikeLike Reply
How could the cDNA been contaminated/damaged before the gel imaging?
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It was likely damaged during our RT-PCR when it was synthesized.
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I enjoyed your presentation! Was there any limitations that resulted in the inconclusive results? Or was it just because the Hypzif failed to work?
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Hi Jesse, thank you! The only limitations were technical errors or malfunctioning materials.
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how do you think the DNA was damanged?
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It was likely damaged during our RT-PCR when the cDNA was synthesized.
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What would you do differently if you were to redo the experiments?
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Hi Kiley! I would have just ensured that the conditions in which these experiments were run were more ideal and that all of the reagents were uncontaminated and functional.
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