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北京泽平
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货号:T_70312356497
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英文名称:X10 CRUCIBLE PORCELAIN MEDIUM FORM CAPACITY 20ML (PACK OF 10)
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文献和实验Isolation, Culture, and Differentiation of Progenitor Cells from the Central Nervous System
5 mL of NEP basal medium, flick the tube, and remove the medium. 9. Add 0.5-1.0 mL of NEP complete medium and triturate 10-20 times, until the tissue pieces are dissociated. More medium may be required, depending
Tracking individual chromosomes with integrated arrays of Lacop sites and GFP-Laci repressor
in which cells are non-covalently attached to a coverslip by a lectin. The chamber medium-filled chamber is assembled as shown in Figure 2B. A flow of fresh medium can be applied; Coat 18mm coverslips with 10µl ConA (1mg/ml in H2 O) and let them air
原代神经细胞培养方法 Neuron Cell Culture
. Freeze 1 ml aliquots of ……UFDU . Freeze 500 m l aliquots of NGF (10 m g/ml Hank’s BSS) Final medium preparation
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