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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
E. Z. N.A.TM X-press Plasmid Protocol
at maximum speed (13,000 x g) for 1 minute to dry the column. 14. Transfer the X-press spin column into a new 1.5 ml centrifuge tube. Add 50 uL Elution Buffer (10mM Tris Hcl pH 8.5) directly onto the center of the membrane. 15. Centrifuge
DNA/RNA/Protein Purification from Cultured Cells Using SQ DNA/RNA/Protein Cell Kit (1-2 x 106 cells)
2. Table top centrifuge capable at least 13,000 x g 3. 1.5 or 2 ml Nuclease-Free centrifuge tubes 4. 0.45 μm filter unit 实验步骤 Before starting: 1. Fresh or flash-frozen cultured cells can be used
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