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I have never performed FISH experiment on Arabidopsis.. I need a detailed protocol.
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I have performed Dot Blot assay, but the background was too high. For washing the membrane PBS-Tween was used. Can anybody suggest other washing buffer?
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When I performed Dot blot assay I always see a "ring signal" in the sonicated DNA sample (positive ctrl). What do you think, how can I avoid this phenomenon?
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I will perform immuofluorescent labelling in Arabidopsis. For DNA stainig I can use SYBR Gold (there is no UV laser in the microscope). Does anyone have experience with SYBR Gold in fixed...
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