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上海希言科学仪器有限公司
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文献和实验of buffers prior to use. Storage Buffer for Column For 500ml 10mM Tris ph 7.5 5ml of 1M 0.3M NaCl150ml 1M or 60ml 2.5M 1mM EDTA 1ml of 0.5M 0.02% NaN3 1ml of 10% CREB Column - Purification Trial #1 Sample #5-C4-1-1 (pg.25)lysed in 4.5ml (3 vol
PCR purification kit) purify DNA through Qiaquick column elute DNA into 50 µl H2 O use 0.5 - 1 µl per 25 µl PCR reaction: 1 x 95 °C, 2 min 21 x 95 °C, 30 sec; 60 °C, 30 sec; 72 °C, 1 min 1 x 72
Linear amplification of limiting amounts of RNA for gene expression studies
with DEPC-H2 O, in case of a bigger volume, speedvac to 8µl. In vitro transcription (IVT) 1 (in RNAse-free PCR tubes) Add the IVT mix consisting of 4µl 5x IVT reaction buffer, 6µl 25mM rNTP mix and 2µl T7 enzyme mix to the ds cDNA (room
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