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文献和实验ChIP protocol for X. laevis Lens1/FoxE3 enhancer
(9) Sonicate the homogenate on ice (10 sec. pulse + 50 sec. break x 6 times, 20% amplitude with a small tip of Branson sonifier (Fisher Dismembranator Model 500)). This step releases chromatin DNA from cells without solubilizing yolk proteins that make
Kodak X-OMAT AR film (XAR) (Fisher, 05-728-41) 14 x17 Kodak X-OMAT AR film (XAR) (Fisher, 05-728-42) 8 x 10 and 14 x 17 intensifying screen (Fisher, FB-IS-810 and FB-IS-1417) ART pipette tips (Rainin) Protocol DNA Preparation/Transfer to Membrane
only the one parameter that I think is the most crucial: the temperature of the annealing step during amplification. My standard PCR reactions are as follows: 5 l template DNA (2-300 ng) 5 l 5 l 10X PCR buffer (10X buffer=100 mM Tris pH 8.3, 500 mM KCl
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