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文献和实验Natural History Museum Protocol for EST sequencing from lamb
- (if the agarose gel in step 4 only shows a weak band, use less than 50µl of water to elute). Direct Purification Buffer: 50mM KCl (=0.37g/100ml) 10mM Tris-HCL (pH 8.8 at 25℃) (=0.12g/100ml) 1.5mM MgCl2 (=0.03g/100ml) 0.1% Triton X-100 (=100µl/100ml
ChIP protocol for X. laevis Lens1/FoxE3 enhancer
1.5 ml 1.2 mM EDTA 0.5M stock 120 µl 1.1% Triton X-100 10% stock 5.5 ml 0.01% SDS 10% stock 50 µl
Natural History Museum Protocol for EST sequencing from lambda zap phage plaques
to collect the eluted DNA in the tube - (if the agarose gel in step 4 only shows a weak band, use less than 50µl of water to elute). Direct Purification Buffer: 50mM KCl (=0.37g/100ml) 10mM Tris-HCL (pH 8.8 at 25oC) (=0.12g/100ml
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