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100 ML BIOSOURCE (TM)
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文献和实验E. Z. N.A.TM X-press Plasmid Protocol
-press spin column inserted in a 2 ml collection tube. 8. Centrifuge at maximum speed (13,000 x g) for 1 minute. 9. Discard the flow-through liquid and re-use the collection tube. 10. Add 500μl DLW Buffer (diluted with isopropanol
Clonality - X Chromosome Inactivation Assay
can be utilized. 1. Materials DNA sample (see Processing of Microdissected Tissue - DNA-based Analysis) Proteinase K (Sigma) Proteinase K buffer (0.05 M Tris-HCL, 0.001 M EDTA, 1% Tween 20, 0.1 mg/ml proteinase K, pH 8.0) Phenol:chloroform:isoamyl alcohol
Preparation of Microinjection Buffer
EDTA, pH 8.0 (autoclaved) 100 mM NaCl 1 ml of 5 M NaCl (autoclaved) 1x Polyamines 50 microliters 1000x Polyamines mix Autoclaved H2O up to 50 ml NOTE: Prepare fresh and discard unused microinjection buffer.
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