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见瓶身
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麦飞生物
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50 ml
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文献和实验A/B/C Random Amplification Protocol
Material DNA fragmentation Part A: Random priming Part B: Dye-primer PCR Hybridization reagents Sau3a (NEB) Sau3a 10x buffer BSA 10 mg/mL Sequenase, T7 DNA pol, 13 U/µ
electrophoresis apparatus and reagents including: Molecular‐biology‐grade agarose TE buffer ( appendix 2A
Native Chromatin Preparation and Illumina/Solexa Library Construction
cell isolation kit) per 107 cells. 12. Mix well and incubate for 15 min at 4°C-8°C. 13. Wash cells with T cell isolation buffer by adding 10X-20X the final labeling volume. Centrifuge at 300g for 10 min. Pipette
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