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- 供应商:
INTEGRA
- 规格:
包
货号:4455
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文献和实验Transformation DNA fragments (or plasmid DNA) into competent E. coli
freezer; thaw on wet ice. 2.Place four 15-ml modified polystylene tubes (PST; Corning disposable sterile centrifuge tube) on ice. 3.Gently mix cells (tapping with fingers), then aliquot 50ʵl competent cells into each of chilled the 15 ml PST. 4.Add
to each well. Mix briefly. 9. Add 100 µl Neutralization buffer to each well. Vortex. 10. Transfer the contents of the deep wells to the waiting filter plates/receiving plate stacks using the wide bore pipette tips provided in the kits. 11
ES Cell Culture and Manipulation
tips (preferably barrier, or plugged tips), a sterile 96well round-bottom plate, plenty of ES cell media, and an inverted microscope in a hood. Aspirate the REF media from the 24-wells and add 2ml of ES cell media to each well. Add 40 µl trypsin-EDTA
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