F actin

... that I have tried that have improved this situation. My supervisor suggest maybe there is contamination of the amplicon I am testing. We use b-actin as a control for a lot of experiments so it is plausible but I find it difficult to believe when in my endpoint PCR I got the negative for that ...

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... that you could have false results because of one-case-only binding/non-binding. To explain - imagine you will design probes for intron in gene for actin. Generaly there are five proteins in spliceosome, let's call them S pliceosome P rotein1 - 5, but in actin is not present SP3, but are present ...

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BTW, It doesn't co-localize with F-actin and microtubes. It seems look like some kind of vesicles. But these vesicles don't like endosomes, golgi or ER, too.

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... and can display rapid electrical responses (action potentials) to environmental stimuli. These action potentials can influence processes such as actin-based cytoplasmic streaming, plant organ movements, wound responses, respiration, photosynthesis and flowering.[2][3][4]" They have an electron ...

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If you were to inhibit microtubules via nocodazole, how would it affect receptor mediated endocytosis. Same scenario with inhibiting actin via cytochalasin-a.

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