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- 2025年07月11日
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文献和实验Technology (ogt) provides good arrays in 4*44k format compatibel with Agilent scanner and hybridisation equipment [5] Hybridisation buffer materials: 5M Sodium chloride Sigma (S6316) 12x MES prepared as follows: 3.52g MES
Preparation of BAC DNA with by Alkaline Prep Method
until the pellet is re-suspended. 4. After all the pellets have been re-suspended (go back to 1st bottle, re-pipette 1-2x to look for clumps), move the bottles from the ice to the bench top. Let them sit for 5 minutes. Solution II: 0.2 M NaOH, 1% SDS (250 ml
【精华】vol 687 Chapter 3 采用Splinkerette-PCR技术对前病毒基因组插入位点进行分离
., and vanLohuizen, M. (2002) Genome-wide retroviral insertional tagging of genes involved in cancer in Cdkn2a-deficient mice. Nat Genet 32, 160–5. 12. Ding, S., Wu, X., Li, G., Han, M., Zhuang,Y., and Xu, T. (2005) Efficient transpositionof the piggyBac (PB
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