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I want to investigate microflora inside of Artemia nauplii, so I want to break the body of Artemia nauplii. what kind of homogenizer machine can I use? Or which method can I use? Thank you so much?
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I perform a plate count but there is no colony on the plate although they still normally proliferated in the MRSB culture. Please tell me why? Thank you so much.
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I did a one dimensional SDS - PAGE. Stacking gel is 5% and Separating Gel is 12%,however, they didn't polimerize. I tried to use progressive concentration of Acrylamide from 12% to 36%, and at 36%...
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I was inoculating Trichoderma in broth culture (submerged inoculation) and I want to determine the spore density? Can somebody help me. Thank you so much!
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