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文献和实验, a pair of frogs were mated (see Grainger Lab X. tropicalis Mating Protocol for details) and the resultant tadpoles were used in the following karyotyping protocol. 2. Place 10 Nieuwkoop & Faber Stage 26-34 tadpoles into a dish of deionized, distilled
Differential Interference Contrast (Nomarski, DIC, Hoffman Modulation Contrast)
that is very common in detritus in ponds and in the solid portion of sewage. The heavily granulated cytoplasm makes a very nice model for observing cytoplasmic streaming. Find the specimen using dark field mode at 40x. Chaos are very large, so this shouldn't
This protocol was provided to us from the Grainger lab and modified by M. Khokha to include the lead brick for better squashing. 1. Place 10 Nieuwkoop & Faber Stage 26-34 tadpoles into a dish of deionized, distilled water.
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