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文献和实验microdissected cells in 20 µl proteinase K buffer.Incubate overnight at 37°C.B: Prepare the Glass PlatesTIP: Use Accuwipes for cleaning purposes, as they will not leave lint behind and are non-abrasive.Clean glass plates twice with glass cleaner.Repeat using 95
Tris(PH=6.8) 10% SDS 40 µl 10% ammonium persulfate 40 µl TEMED 7 µl C. Preparation of gel 1. Assemble the glass plates and spacers (0.75 mm thick). 2. Pour the running gel to about 1 cm below the wells of the comb (~3.2 ml). 3. Seal with 1 ml
Lipoprotein Isolation - First week
glass beaker. To get maximum yield, it is necessary to flush out the blood by injecting buffer into the body cavity. The experimental procedure is schematically shown in the following figure. Following the removal of hemocytes, potassium
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